Canonical Allele Identifier: CA344030353

Gene: CRB1

Linked Data

• dbSNP Id: rs1558125488
• gnomAD v4: 1-197421144-C-A
• COSMIC: COSM4616171 ; COSM4616172
• MyVariant Identifiers: chr1:g.197390274C>A (hg19) ; chr1:g.197421144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421144C>A , CM000663.2:g.197421144C>A	GRCh38
NC_000001.10:g.197390274C>A , CM000663.1:g.197390274C>A	GRCh37
NC_000001.9:g.195656897C>A	NCBI36
NG_008483.1:g.157867C>A
NG_008483.2:g.224683C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1316C>A MANE Select	ENSP00000356370.3:p.Ser439Tyr
ENST00000638467.1:c.1316C>A	ENSP00000491102.1:p.Ser439Tyr
ENST00000681519.1:c.197C>A	ENSP00000505267.1:p.Ser66Tyr
ENST00000367397.1:c.-542C>A	ENSP00000356367.1:n.-542C>A
ENST00000367399.6:c.980C>A	ENSP00000356369.2:p.Ser327Tyr
ENST00000367400.7:c.1316C>A	ENSP00000356370.3:p.Ser439Tyr
ENST00000476483.1:n.276C>A
ENST00000484075.5:c.1316C>A	ENSP00000433932.1:p.Ser439Tyr
ENST00000535699.5:c.1109C>A	ENSP00000438786.1:p.Ser370Tyr
ENST00000538660.5:c.1316C>A	ENSP00000438091.1:p.Ser439Tyr
NM_001193640.1:c.980C>A	NP_001180569.1:p.Ser327Tyr
NM_001257965.1:c.1109C>A	NP_001244894.1:p.Ser370Tyr
NM_001257966.1:c.1316C>A	NP_001244895.1:p.Ser439Tyr
NM_201253.2:c.1316C>A	NP_957705.1:p.Ser439Tyr
NR_047563.1:n.1525C>A
NR_047564.1:n.1525C>A
XM_011509365.1:c.1316C>A	XP_011507667.1:p.Ser439Tyr
XM_011509366.1:c.1316C>A	XP_011507668.1:p.Ser439Tyr
XM_011509367.1:c.1316C>A	XP_011507669.1:p.Ser439Tyr
XM_011509368.1:c.734C>A	XP_011507670.1:p.Ser245Tyr
XM_011509369.1:c.-242C>A	XP_011507671.1:n.-242C>A
XM_011509365.2:c.1316C>A	XP_011507667.1:p.Ser439Tyr
XM_011509369.2:c.-242C>A	XP_011507671.1:n.-242C>A
XM_017000851.1:c.473C>A	XP_016856340.1:p.Ser158Tyr
XM_017000852.1:c.1316C>A	XP_016856341.1:p.Ser439Tyr
NM_201253.3:c.1316C>A MANE Select	NP_957705.1:p.Ser439Tyr
NM_001193640.2:c.980C>A	NP_001180569.1:p.Ser327Tyr
NM_001257965.2:c.1109C>A	NP_001244894.1:p.Ser370Tyr
NR_047563.2:n.1477C>A
NR_047564.2:n.1477C>A
NM_001257966.2:c.1316C>A	NP_001244895.1:p.Ser439Tyr