Canonical Allele Identifier: CA1218063001

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421086A= , CM000663.2:g.197421086A=	GRCh38
NC_000001.10:g.197390216A= , CM000663.1:g.197390216A=	GRCh37
NC_000001.9:g.195656839A=	NCBI36
NG_008483.1:g.157809A=
NG_008483.2:g.224625A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1258A= MANE Select	ENSP00000356370.3:p.Thr420=
ENST00000638467.1:c.1258A=	ENSP00000491102.1:p.Thr420=
ENST00000681519.1:c.139A=	ENSP00000505267.1:p.Thr47=
ENST00000367397.1:c.-600A=	ENSP00000356367.1:n.-600A=
ENST00000367399.6:c.922A=	ENSP00000356369.2:p.Thr308=
ENST00000367400.7:c.1258A=	ENSP00000356370.3:p.Thr420=
ENST00000476483.1:n.218A=
ENST00000484075.5:c.1258A=	ENSP00000433932.1:p.Thr420=
ENST00000535699.5:c.1051A=	ENSP00000438786.1:p.Thr351=
ENST00000538660.5:c.1258A=	ENSP00000438091.1:p.Thr420=
NM_001193640.1:c.922A=	NP_001180569.1:p.Thr308=
NM_001257965.1:c.1051A=	NP_001244894.1:p.Thr351=
NM_001257966.1:c.1258A=	NP_001244895.1:p.Thr420=
NM_201253.2:c.1258A=	NP_957705.1:p.Thr420=
NR_047563.1:n.1467A=
NR_047564.1:n.1467A=
XM_011509365.1:c.1258A=	XP_011507667.1:p.Thr420=
XM_011509366.1:c.1258A=	XP_011507668.1:p.Thr420=
XM_011509367.1:c.1258A=	XP_011507669.1:p.Thr420=
XM_011509368.1:c.676A=	XP_011507670.1:p.Thr226=
XM_011509369.1:c.-300A=	XP_011507671.1:n.-300A=
XM_011509365.2:c.1258A=	XP_011507667.1:p.Thr420=
XM_011509369.2:c.-300A=	XP_011507671.1:n.-300A=
XM_017000851.1:c.415A=	XP_016856340.1:p.Thr139=
XM_017000852.1:c.1258A=	XP_016856341.1:p.Thr420=
NM_201253.3:c.1258A= MANE Select	NP_957705.1:p.Thr420=
NM_001193640.2:c.922A=	NP_001180569.1:p.Thr308=
NM_001257965.2:c.1051A=	NP_001244894.1:p.Thr351=
NR_047563.2:n.1419A=
NR_047564.2:n.1419A=
NM_001257966.2:c.1258A=	NP_001244895.1:p.Thr420=