Canonical Allele Identifier: CA2186513746

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811818T= , CM000677.2:g.71811818T=	GRCh38
NC_000015.9:g.72104158T= , CM000677.1:g.72104158T=	GRCh37
NC_000015.8:g.69891212T=	NCBI36
NG_009113.2:g.6264T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.298T= MANE Select	ENSP00000482504.1:p.Cys100=
ENST00000617575.4:c.298T=	ENSP00000482504.1:p.Cys100=
ENST00000621098.1:c.298T=	ENSP00000479962.1:p.Cys100=
ENST00000621736.4:c.34T=	ENSP00000479254.1:p.Cys12=
NM_014249.3:c.298T=	NP_055064.1:p.Cys100=
NM_016346.3:c.298T=	NP_057430.1:p.Cys100=
XM_011521146.1:c.34T=	XP_011519448.1:p.Cys12=
NM_014249.4:c.298T= MANE Select	NP_055064.1:p.Cys100=
NM_016346.4:c.298T=	NP_057430.1:p.Cys100=