Variant position: 1028 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:
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 VAVLQPYIFVATVPVIVAFI MLRAYFLQTSQQLKQLESEGR
Gorilla VAVLQPYIFVATVPVIVAFI MLRAYFLQTSQQLKQLESEGR
Rhesus macaque VAVLQPYIFVATVPVIVAFI MLRAYFLQTSQQLKQLESEGR
Chimpanzee VAVLQPYIFVATVPVIVAFI MLRAYFLQTSQQLKQLESEGR
Mouse VSALQPYIFLATVPGLVVFI LLRAYFLHTAQQLKQLESEGR
Rat VSALQPYIFLATVPGLAVFI LLRAYFLHTSQQLKQLESEGR
Pig VSVLKPYIFLATVPVIVAFI LLRAYFLHTSQQLKQLESEGR
Bovine VSVLQPYIFLATVPVIAAFI LLRAYFLHTSQQLKQLESEGR
Rabbit VSVLQPYIFLATVPVIAAFI LLRAYFLHTSQQLKQLESEGR
Sheep VSVLQPYIFLATVPVIAAFI LLRGYFLHTSQQLKQLESEGR
Horse VSVLQPYIFLATVPVIAAFI ILRAYFLHTSQQLKQLESEGR
Xenopus laevis VSLLEPYIFLATVPVIVAFI LLRSYFLHTSQQLKQLESKAR
Zebrafish VSIVRPYIFLAATPLAIIFI VMRKYFLRTGQQLKQLETEAR
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
1 – 1480 Cystic fibrosis transmembrane conductance regulator
1014 – 1034 Helical; Name=10
859 – 1155 ABC transmembrane type-1 2
606 – 1480 Missing. In isoform 3.
1014 – 1046
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I).
Onay T.; Topaloglu O.; Zielenski J.; Gokgoz N.; Kayserili H.; Camcioglu Y.; Cokugras H.; Akcakaya N.; Apak M.; Tsui L.-C.; Kirdar B.;
Hum. Genet. 102:224-230(1998)
Cited for: VARIANTS CF LEU-1013 AND ILE-1028;
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.