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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q16602: Variant p.Tyr8Asn

Calcitonin gene-related peptide type 1 receptor
Gene: CALCRL
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Variant information Variant position: help 8 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LB/B The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Tyrosine (Y) to Asparagine (N) at position 8 (Y8N, p.Tyr8Asn). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from large size and aromatic (Y) to medium size and polar (N) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 8 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 461 The length of the canonical sequence.
Location on the sequence: help MEKKCTL Y FLVLLPFFMILVTAELEESP The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         MEKKCTLYFLVLL---PFFMIL---VTAEL-EES--P-

Mouse                         MDKKHILCFLVLL---PLNMAL---ISA

Rat                           MDKKCTLCFLFLL---LLNMAL---IAA

Pig                           MEKKYILYFLFLL---PFFMIL---VIA

Bovine                        MEKKFFLSFLFLL---PFFMIL---VIA

Xenopus laevis                LSRSALFKYIIIF---LIMINTRGYVLA

Xenopus tropicalis            LLRSALFKYIIIV---LIMLNLRGYVLA

Zebrafish                     MTASCWTICLFLLGSVTEFIVLASPEVN

Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Signal peptide 1 – 22



Literature citations
A cDNA encoding the calcitonin gene-related peptide type 1 receptor.
Aiyar N.; Rand K.; Elshourbagy N.A.; Zeng Z.; Adamou J.E.; Bergsma D.J.; Li Y.;
J. Biol. Chem. 271:11325-11329(1996)
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; VARIANT ASN-8; A human orphan calcitonin receptor-like structure.
Fluehmann B.; Muff R.; Hunziker W.; Fischer J.A.; Born W.;
Biochem. Biophys. Res. Commun. 206:341-347(1995)
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; VARIANT ASN-8; cDNA clones of human proteins involved in signal transduction sequenced by the Guthrie cDNA resource center (www.cdna.org).
Kopatz S.A.; Aronstam R.S.; Sharma S.V.;
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]; VARIANT ASN-8;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.