Canonical Allele Identifier: CA1218065298

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429370C= , CM000663.2:g.197429370C=	GRCh38
NC_000001.10:g.197398500C= , CM000663.1:g.197398500C=	GRCh37
NC_000001.9:g.195665123C=	NCBI36
NG_008483.1:g.166093C=
NG_008483.2:g.232909C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2677-79C= MANE Select	ENSP00000356370.3:n.2677-79C=
ENST00000638467.1:c.2677-79C=	ENSP00000491102.1:n.2677-79C=
ENST00000681519.1:c.1558-79C=	ENSP00000505267.1:n.1558-79C=
ENST00000367397.1:c.820-79C=	ENSP00000356367.1:n.820-79C=
ENST00000367399.6:c.2341-79C=	ENSP00000356369.2:n.2341-79C=
ENST00000367400.7:c.2677-79C=	ENSP00000356370.3:n.2677-79C=
ENST00000484075.5:c.2677-79C=	ENSP00000433932.1:n.2677-79C=
ENST00000535699.5:c.2605-79C=	ENSP00000438786.1:n.2605-79C=
ENST00000538660.5:c.2129-6230C=	ENSP00000438091.1:n.2129-6230C=
NM_001193640.1:c.2341-79C=	NP_001180569.1:n.2341-79C=
NM_001257965.1:c.2605-79C=	NP_001244894.1:n.2605-79C=
NM_001257966.1:c.2129-6230C=	NP_001244895.1:n.2129-6230C=
NM_201253.2:c.2677-79C=	NP_957705.1:n.2677-79C=
NR_047563.1:n.2678-79C=
NR_047564.1:n.2886-79C=
XM_011509365.1:c.2677-79C=	XP_011507667.1:n.2677-79C=
XM_011509366.1:c.2677-79C=	XP_011507668.1:n.2677-79C=
XM_011509367.1:c.2677-79C=	XP_011507669.1:n.2677-79C=
XM_011509368.1:c.2095-79C=	XP_011507670.1:n.2095-79C=
XM_011509369.1:c.1120-79C=	XP_011507671.1:n.1120-79C=
XM_011509365.2:c.2677-79C=	XP_011507667.1:n.2677-79C=
XM_011509369.2:c.1120-79C=	XP_011507671.1:n.1120-79C=
XM_017000851.1:c.1834-79C=	XP_016856340.1:n.1834-79C=
XM_017000852.1:c.2812-79C=	XP_016856341.1:n.2812-79C=
NM_201253.3:c.2677-79C= MANE Select	NP_957705.1:n.2677-79C=
NM_001193640.2:c.2341-79C=	NP_001180569.1:n.2341-79C=
NM_001257965.2:c.2605-79C=	NP_001244894.1:n.2605-79C=
NR_047563.2:n.2630-79C=
NR_047564.2:n.2838-79C=
NM_001257966.2:c.2129-6230C=	NP_001244895.1:n.2129-6230C=