Canonical Allele Identifier: CA1218063026

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421147A= , CM000663.2:g.197421147A=	GRCh38
NC_000001.10:g.197390277A= , CM000663.1:g.197390277A=	GRCh37
NC_000001.9:g.195656900A=	NCBI36
NG_008483.1:g.157870A=
NG_008483.2:g.224686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1319A= MANE Select	ENSP00000356370.3:p.Asp440=
ENST00000638467.1:c.1319A=	ENSP00000491102.1:p.Asp440=
ENST00000681519.1:c.200A=	ENSP00000505267.1:p.Asp67=
ENST00000367397.1:c.-539A=	ENSP00000356367.1:n.-539A=
ENST00000367399.6:c.983A=	ENSP00000356369.2:p.Asp328=
ENST00000367400.7:c.1319A=	ENSP00000356370.3:p.Asp440=
ENST00000476483.1:n.279A=
ENST00000484075.5:c.1319A=	ENSP00000433932.1:p.Asp440=
ENST00000535699.5:c.1112A=	ENSP00000438786.1:p.Asp371=
ENST00000538660.5:c.1319A=	ENSP00000438091.1:p.Asp440=
NM_001193640.1:c.983A=	NP_001180569.1:p.Asp328=
NM_001257965.1:c.1112A=	NP_001244894.1:p.Asp371=
NM_001257966.1:c.1319A=	NP_001244895.1:p.Asp440=
NM_201253.2:c.1319A=	NP_957705.1:p.Asp440=
NR_047563.1:n.1528A=
NR_047564.1:n.1528A=
XM_011509365.1:c.1319A=	XP_011507667.1:p.Asp440=
XM_011509366.1:c.1319A=	XP_011507668.1:p.Asp440=
XM_011509367.1:c.1319A=	XP_011507669.1:p.Asp440=
XM_011509368.1:c.737A=	XP_011507670.1:p.Asp246=
XM_011509369.1:c.-239A=	XP_011507671.1:n.-239A=
XM_011509365.2:c.1319A=	XP_011507667.1:p.Asp440=
XM_011509369.2:c.-239A=	XP_011507671.1:n.-239A=
XM_017000851.1:c.476A=	XP_016856340.1:p.Asp159=
XM_017000852.1:c.1319A=	XP_016856341.1:p.Asp440=
NM_201253.3:c.1319A= MANE Select	NP_957705.1:p.Asp440=
NM_001193640.2:c.983A=	NP_001180569.1:p.Asp328=
NM_001257965.2:c.1112A=	NP_001244894.1:p.Asp371=
NR_047563.2:n.1480A=
NR_047564.2:n.1480A=
NM_001257966.2:c.1319A=	NP_001244895.1:p.Asp440=