Canonical Allele Identifier: CA1218068707

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434879T= , CM000663.2:g.197434879T=	GRCh38
NC_000001.10:g.197404009T= , CM000663.1:g.197404009T=	GRCh37
NC_000001.9:g.195670632T=	NCBI36
NG_008483.1:g.171602T=
NG_008483.2:g.238418T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3016T= MANE Select	ENSP00000356370.3:p.Ser1006=
ENST00000638467.1:c.3016T=	ENSP00000491102.1:p.Ser1006=
ENST00000681519.1:c.1897T=	ENSP00000505267.1:p.Ser633=
ENST00000367397.1:c.1159T=	ENSP00000356367.1:p.Ser387=
ENST00000367399.6:c.2680T=	ENSP00000356369.2:p.Ser894=
ENST00000367400.7:c.3016T=	ENSP00000356370.3:p.Ser1006=
ENST00000484075.5:c.3016T=	ENSP00000433932.1:p.Ser1006=
ENST00000535699.5:c.2944T=	ENSP00000438786.1:p.Ser982=
ENST00000538660.5:c.2129-721T=	ENSP00000438091.1:n.2129-721T=
NM_001193640.1:c.2680T=	NP_001180569.1:p.Ser894=
NM_001257965.1:c.2944T=	NP_001244894.1:p.Ser982=
NM_001257966.1:c.2129-721T=	NP_001244895.1:n.2129-721T=
NM_201253.2:c.3016T=	NP_957705.1:p.Ser1006=
NR_047563.1:n.3017T=
NR_047564.1:n.3225T=
XM_011509365.1:c.3016T=	XP_011507667.1:p.Ser1006=
XM_011509366.1:c.3016T=	XP_011507668.1:p.Ser1006=
XM_011509367.1:c.3016T=	XP_011507669.1:p.Ser1006=
XM_011509368.1:c.2434T=	XP_011507670.1:p.Ser812=
XM_011509369.1:c.1459T=	XP_011507671.1:p.Ser487=
XM_011509365.2:c.3016T=	XP_011507667.1:p.Ser1006=
XM_011509369.2:c.1459T=	XP_011507671.1:p.Ser487=
XM_017000851.1:c.2173T=	XP_016856340.1:p.Ser725=
XM_017000852.1:c.3151T=	XP_016856341.1:p.Ser1051=
NM_201253.3:c.3016T= MANE Select	NP_957705.1:p.Ser1006=
NM_001193640.2:c.2680T=	NP_001180569.1:p.Ser894=
NM_001257965.2:c.2944T=	NP_001244894.1:p.Ser982=
NR_047563.2:n.2969T=
NR_047564.2:n.3177T=
NM_001257966.2:c.2129-721T=	NP_001244895.1:n.2129-721T=