Canonical Allele Identifier: CA344031073
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421302G>T , CM000663.2:g.197421302G>T GRCh38
NC_000001.10:g.197390432G>T , CM000663.1:g.197390432G>T GRCh37
NC_000001.9:g.195657055G>T NCBI36
NG_008483.1:g.158025G>T
NG_008483.2:g.224841G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1474G>T MANE Select ENSP00000356370.3:p.Gly492Cys
ENST00000638467.1:c.1474G>T ENSP00000491102.1:p.Gly492Cys
ENST00000681519.1:c.355G>T ENSP00000505267.1:p.Gly119Cys
ENST00000367397.1:c.-384G>T ENSP00000356367.1:n.-384G>T
ENST00000367399.6:c.1138G>T ENSP00000356369.2:p.Gly380Cys
ENST00000367400.7:c.1474G>T ENSP00000356370.3:p.Gly492Cys
ENST00000476483.1:n.434G>T
ENST00000484075.5:c.1474G>T ENSP00000433932.1:p.Gly492Cys
ENST00000535699.5:c.1267G>T ENSP00000438786.1:p.Gly423Cys
ENST00000538660.5:c.1474G>T ENSP00000438091.1:p.Gly492Cys
NM_001193640.1:c.1138G>T NP_001180569.1:p.Gly380Cys
NM_001257965.1:c.1267G>T NP_001244894.1:p.Gly423Cys
NM_001257966.1:c.1474G>T NP_001244895.1:p.Gly492Cys
NM_201253.2:c.1474G>T NP_957705.1:p.Gly492Cys
NR_047563.1:n.1683G>T
NR_047564.1:n.1683G>T
XM_011509365.1:c.1474G>T XP_011507667.1:p.Gly492Cys
XM_011509366.1:c.1474G>T XP_011507668.1:p.Gly492Cys
XM_011509367.1:c.1474G>T XP_011507669.1:p.Gly492Cys
XM_011509368.1:c.892G>T XP_011507670.1:p.Gly298Cys
XM_011509369.1:c.-84G>T XP_011507671.1:n.-84G>T
XM_011509365.2:c.1474G>T XP_011507667.1:p.Gly492Cys
XM_011509369.2:c.-84G>T XP_011507671.1:n.-84G>T
XM_017000851.1:c.631G>T XP_016856340.1:p.Gly211Cys
XM_017000852.1:c.1474G>T XP_016856341.1:p.Gly492Cys
NM_201253.3:c.1474G>T MANE Select NP_957705.1:p.Gly492Cys
NM_001193640.2:c.1138G>T NP_001180569.1:p.Gly380Cys
NM_001257965.2:c.1267G>T NP_001244894.1:p.Gly423Cys
NR_047563.2:n.1635G>T
NR_047564.2:n.1635G>T
NM_001257966.2:c.1474G>T NP_001244895.1:p.Gly492Cys