Sequence information
Variant position: 311 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1480 The length of the canonical sequence.
Location on the sequence:
TELKLTRKAAYVRYFNSSAF
F FSGFFVVFLSVLPYALIKGI
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: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALIKGI
Gorilla TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALIKGI
Rhesus macaque TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALIKGI
Chimpanzee TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALIKGI
Mouse VELKMTRKAAYMRFFTSSAFF FSGFFVVFLSVLPYTVINGI
Rat EELKMTRRSAYMRFFTSSAFF FSGFFVVFLSVLPYTVINGI
Pig TELKLTRKAAYVRYFNSSAFF FSGLFVVFLSVLPYALLKGI
Bovine TELKLTRKAAYVRYLNSSAFF FSGFFVVFLSVLPYALLKGI
Rabbit TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALTKGI
Sheep TELKLTRKAAYVRYLNSSAFF FSGFFVVFLSVLPYALLKGI
Horse TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSVLPYALIKGI
Xenopus laevis TELKLTRKAAYVRYFNSSAFF FSGFFVVFLSIVPHLLLDGI
Zebrafish DEVKLTRKIGSLRYFYSSAYF FSAIFVIVAAVVPHALSRGI
Sequence annotation in neighborhood: 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.
Type Positions Description
Chain
1 – 1480
Cystic fibrosis transmembrane conductance regulator
Transmembrane
299 – 319
Helical; Name=5
Domain
81 – 365
ABC transmembrane type-1 1
Helix
278 – 312
Literature citations
No reference for the current variant in UniProtKB/Swiss-Prot.
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.