Canonical Allele Identifier: CA344037203
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427735A>T , CM000663.2:g.197427735A>T GRCh38
NC_000001.10:g.197396865A>T , CM000663.1:g.197396865A>T GRCh37
NC_000001.9:g.195663488A>T NCBI36
NG_008483.1:g.164458A>T
NG_008483.2:g.231274A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367400.8:c.2410A>T MANE Select ENSP00000356370.3:p.Lys804Ter
ENST00000638467.1:c.2410A>T ENSP00000491102.1:p.Lys804Ter
ENST00000681519.1:c.1291A>T ENSP00000505267.1:p.Lys431Ter
ENST00000367397.1:c.553A>T ENSP00000356367.1:p.Lys185Ter
ENST00000367399.6:c.2074A>T ENSP00000356369.2:p.Lys692Ter
ENST00000367400.7:c.2410A>T ENSP00000356370.3:p.Lys804Ter
ENST00000480086.2:n.311A>T
ENST00000484075.5:c.2410A>T ENSP00000433932.1:p.Lys804Ter
ENST00000535699.5:c.2203A>T ENSP00000438786.1:p.Lys735Ter
ENST00000538660.5:c.2128+5779A>T ENSP00000438091.1:n.2128+5779A>T
NM_001193640.1:c.2074A>T NP_001180569.1:p.Lys692Ter
NM_001257965.1:c.2203A>T NP_001244894.1:p.Lys735Ter
NM_001257966.1:c.2128+5779A>T NP_001244895.1:n.2128+5779A>T
NM_201253.2:c.2410A>T NP_957705.1:p.Lys804Ter
NR_047563.1:n.2411A>T
NR_047564.1:n.2619A>T
XM_011509365.1:c.2410A>T XP_011507667.1:p.Lys804Ter
XM_011509366.1:c.2410A>T XP_011507668.1:p.Lys804Ter
XM_011509367.1:c.2410A>T XP_011507669.1:p.Lys804Ter
XM_011509368.1:c.1828A>T XP_011507670.1:p.Lys610Ter
XM_011509369.1:c.853A>T XP_011507671.1:p.Lys285Ter
XM_011509365.2:c.2410A>T XP_011507667.1:p.Lys804Ter
XM_011509369.2:c.853A>T XP_011507671.1:p.Lys285Ter
XM_017000851.1:c.1567A>T XP_016856340.1:p.Lys523Ter
XM_017000852.1:c.2410A>T XP_016856341.1:p.Lys804Ter
NM_201253.3:c.2410A>T MANE Select NP_957705.1:p.Lys804Ter
NM_001193640.2:c.2074A>T NP_001180569.1:p.Lys692Ter
NM_001257965.2:c.2203A>T NP_001244894.1:p.Lys735Ter
NR_047563.2:n.2363A>T
NR_047564.2:n.2571A>T
NM_001257966.2:c.2128+5779A>T NP_001244895.1:n.2128+5779A>T