Canonical Allele Identifier: CA1311914
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs769475443

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421213A>G , CM000663.2:g.197421213A>G GRCh38
NC_000001.10:g.197390343A>G , CM000663.1:g.197390343A>G GRCh37
NC_000001.9:g.195656966A>G NCBI36
NG_008483.1:g.157936A>G
NG_008483.2:g.224752A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1385A>G MANE Select ENSP00000356370.3:p.Asp462Gly
ENST00000638467.1:c.1385A>G ENSP00000491102.1:p.Asp462Gly
ENST00000681519.1:c.266A>G ENSP00000505267.1:p.Asp89Gly
ENST00000367397.1:c.-473A>G ENSP00000356367.1:n.-473A>G
ENST00000367399.6:c.1049A>G ENSP00000356369.2:p.Asp350Gly
ENST00000367400.7:c.1385A>G ENSP00000356370.3:p.Asp462Gly
ENST00000476483.1:n.345A>G
ENST00000484075.5:c.1385A>G ENSP00000433932.1:p.Asp462Gly
ENST00000535699.5:c.1178A>G ENSP00000438786.1:p.Asp393Gly
ENST00000538660.5:c.1385A>G ENSP00000438091.1:p.Asp462Gly
NM_001193640.1:c.1049A>G NP_001180569.1:p.Asp350Gly
NM_001257965.1:c.1178A>G NP_001244894.1:p.Asp393Gly
NM_001257966.1:c.1385A>G NP_001244895.1:p.Asp462Gly
NM_201253.2:c.1385A>G NP_957705.1:p.Asp462Gly
NR_047563.1:n.1594A>G
NR_047564.1:n.1594A>G
XM_011509365.1:c.1385A>G XP_011507667.1:p.Asp462Gly
XM_011509366.1:c.1385A>G XP_011507668.1:p.Asp462Gly
XM_011509367.1:c.1385A>G XP_011507669.1:p.Asp462Gly
XM_011509368.1:c.803A>G XP_011507670.1:p.Asp268Gly
XM_011509369.1:c.-173A>G XP_011507671.1:n.-173A>G
XM_011509365.2:c.1385A>G XP_011507667.1:p.Asp462Gly
XM_011509369.2:c.-173A>G XP_011507671.1:n.-173A>G
XM_017000851.1:c.542A>G XP_016856340.1:p.Asp181Gly
XM_017000852.1:c.1385A>G XP_016856341.1:p.Asp462Gly
NM_201253.3:c.1385A>G MANE Select NP_957705.1:p.Asp462Gly
NM_001193640.2:c.1049A>G NP_001180569.1:p.Asp350Gly
NM_001257965.2:c.1178A>G NP_001244894.1:p.Asp393Gly
NR_047563.2:n.1546A>G
NR_047564.2:n.1546A>G
NM_001257966.2:c.1385A>G NP_001244895.1:p.Asp462Gly