Canonical Allele Identifier: CA344037047
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1418893083

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427685T>C , CM000663.2:g.197427685T>C GRCh38
NC_000001.10:g.197396815T>C , CM000663.1:g.197396815T>C GRCh37
NC_000001.9:g.195663438T>C NCBI36
NG_008483.1:g.164408T>C
NG_008483.2:g.231224T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2360T>C MANE Select ENSP00000356370.3:p.Val787Ala
ENST00000638467.1:c.2360T>C ENSP00000491102.1:p.Val787Ala
ENST00000681519.1:c.1241T>C ENSP00000505267.1:p.Val414Ala
ENST00000367397.1:c.503T>C ENSP00000356367.1:p.Val168Ala
ENST00000367399.6:c.2024T>C ENSP00000356369.2:p.Val675Ala
ENST00000367400.7:c.2360T>C ENSP00000356370.3:p.Val787Ala
ENST00000480086.2:n.261T>C
ENST00000484075.5:c.2360T>C ENSP00000433932.1:p.Val787Ala
ENST00000535699.5:c.2153T>C ENSP00000438786.1:p.Val718Ala
ENST00000538660.5:c.2128+5729T>C ENSP00000438091.1:n.2128+5729T>C
NM_001193640.1:c.2024T>C NP_001180569.1:p.Val675Ala
NM_001257965.1:c.2153T>C NP_001244894.1:p.Val718Ala
NM_001257966.1:c.2128+5729T>C NP_001244895.1:n.2128+5729T>C
NM_201253.2:c.2360T>C NP_957705.1:p.Val787Ala
NR_047563.1:n.2361T>C
NR_047564.1:n.2569T>C
XM_011509365.1:c.2360T>C XP_011507667.1:p.Val787Ala
XM_011509366.1:c.2360T>C XP_011507668.1:p.Val787Ala
XM_011509367.1:c.2360T>C XP_011507669.1:p.Val787Ala
XM_011509368.1:c.1778T>C XP_011507670.1:p.Val593Ala
XM_011509369.1:c.803T>C XP_011507671.1:p.Val268Ala
XM_011509365.2:c.2360T>C XP_011507667.1:p.Val787Ala
XM_011509369.2:c.803T>C XP_011507671.1:p.Val268Ala
XM_017000851.1:c.1517T>C XP_016856340.1:p.Val506Ala
XM_017000852.1:c.2360T>C XP_016856341.1:p.Val787Ala
NM_201253.3:c.2360T>C MANE Select NP_957705.1:p.Val787Ala
NM_001193640.2:c.2024T>C NP_001180569.1:p.Val675Ala
NM_001257965.2:c.2153T>C NP_001244894.1:p.Val718Ala
NR_047563.2:n.2313T>C
NR_047564.2:n.2521T>C
NM_001257966.2:c.2128+5729T>C NP_001244895.1:n.2128+5729T>C