Canonical Allele Identifier: CA1218062976

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421008T= , CM000663.2:g.197421008T=	GRCh38
NC_000001.10:g.197390138T= , CM000663.1:g.197390138T=	GRCh37
NC_000001.9:g.195656761T=	NCBI36
NG_008483.1:g.157731T=
NG_008483.2:g.224547T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1180T= MANE Select	ENSP00000356370.3:p.Cys394=
ENST00000638467.1:c.1180T=	ENSP00000491102.1:p.Cys394=
ENST00000681519.1:c.61T=	ENSP00000505267.1:p.Cys21=
ENST00000367397.1:c.-678T=	ENSP00000356367.1:n.-678T=
ENST00000367399.6:c.844T=	ENSP00000356369.2:p.Cys282=
ENST00000367400.7:c.1180T=	ENSP00000356370.3:p.Cys394=
ENST00000476483.1:n.140T=
ENST00000484075.5:c.1180T=	ENSP00000433932.1:p.Cys394=
ENST00000535699.5:c.973T=	ENSP00000438786.1:p.Cys325=
ENST00000538660.5:c.1180T=	ENSP00000438091.1:p.Cys394=
NM_001193640.1:c.844T=	NP_001180569.1:p.Cys282=
NM_001257965.1:c.973T=	NP_001244894.1:p.Cys325=
NM_001257966.1:c.1180T=	NP_001244895.1:p.Cys394=
NM_201253.2:c.1180T=	NP_957705.1:p.Cys394=
NR_047563.1:n.1389T=
NR_047564.1:n.1389T=
XM_011509365.1:c.1180T=	XP_011507667.1:p.Cys394=
XM_011509366.1:c.1180T=	XP_011507668.1:p.Cys394=
XM_011509367.1:c.1180T=	XP_011507669.1:p.Cys394=
XM_011509368.1:c.598T=	XP_011507670.1:p.Cys200=
XM_011509369.1:c.-378T=	XP_011507671.1:n.-378T=
XM_011509365.2:c.1180T=	XP_011507667.1:p.Cys394=
XM_011509369.2:c.-378T=	XP_011507671.1:n.-378T=
XM_017000851.1:c.337T=	XP_016856340.1:p.Cys113=
XM_017000852.1:c.1180T=	XP_016856341.1:p.Cys394=
NM_201253.3:c.1180T= MANE Select	NP_957705.1:p.Cys394=
NM_001193640.2:c.844T=	NP_001180569.1:p.Cys282=
NM_001257965.2:c.973T=	NP_001244894.1:p.Cys325=
NR_047563.2:n.1341T=
NR_047564.2:n.1341T=
NM_001257966.2:c.1180T=	NP_001244895.1:p.Cys394=