Canonical Allele Identifier: CA1218066285

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427799A= , CM000663.2:g.197427799A=	GRCh38
NC_000001.10:g.197396929A= , CM000663.1:g.197396929A=	GRCh37
NC_000001.9:g.195663552A=	NCBI36
NG_008483.1:g.164522A=
NG_008483.2:g.231338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2474A= MANE Select	ENSP00000356370.3:p.Glu825=
ENST00000638467.1:c.2474A=	ENSP00000491102.1:p.Glu825=
ENST00000681519.1:c.1355A=	ENSP00000505267.1:p.Glu452=
ENST00000367397.1:c.617A=	ENSP00000356367.1:p.Glu206=
ENST00000367399.6:c.2138A=	ENSP00000356369.2:p.Glu713=
ENST00000367400.7:c.2474A=	ENSP00000356370.3:p.Glu825=
ENST00000480086.2:n.375A=
ENST00000484075.5:c.2474A=	ENSP00000433932.1:p.Glu825=
ENST00000535699.5:c.2267A=	ENSP00000438786.1:p.Glu756=
ENST00000538660.5:c.2128+5843A=	ENSP00000438091.1:n.2128+5843A=
NM_001193640.1:c.2138A=	NP_001180569.1:p.Glu713=
NM_001257965.1:c.2267A=	NP_001244894.1:p.Glu756=
NM_001257966.1:c.2128+5843A=	NP_001244895.1:n.2128+5843A=
NM_201253.2:c.2474A=	NP_957705.1:p.Glu825=
NR_047563.1:n.2475A=
NR_047564.1:n.2683A=
XM_011509365.1:c.2474A=	XP_011507667.1:p.Glu825=
XM_011509366.1:c.2474A=	XP_011507668.1:p.Glu825=
XM_011509367.1:c.2474A=	XP_011507669.1:p.Glu825=
XM_011509368.1:c.1892A=	XP_011507670.1:p.Glu631=
XM_011509369.1:c.917A=	XP_011507671.1:p.Glu306=
XM_011509365.2:c.2474A=	XP_011507667.1:p.Glu825=
XM_011509369.2:c.917A=	XP_011507671.1:p.Glu306=
XM_017000851.1:c.1631A=	XP_016856340.1:p.Glu544=
XM_017000852.1:c.2474A=	XP_016856341.1:p.Glu825=
NM_201253.3:c.2474A= MANE Select	NP_957705.1:p.Glu825=
NM_001193640.2:c.2138A=	NP_001180569.1:p.Glu713=
NM_001257965.2:c.2267A=	NP_001244894.1:p.Glu756=
NR_047563.2:n.2427A=
NR_047564.2:n.2635A=
NM_001257966.2:c.2128+5843A=	NP_001244895.1:n.2128+5843A=