Canonical Allele Identifier: CA2186513742

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811809C= , CM000677.2:g.71811809C=	GRCh38
NC_000015.9:g.72104149C= , CM000677.1:g.72104149C=	GRCh37
NC_000015.8:g.69891203C=	NCBI36
NG_009113.2:g.6255C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.289C= MANE Select	ENSP00000482504.1:p.Arg97=
ENST00000617575.4:c.289C=	ENSP00000482504.1:p.Arg97=
ENST00000621098.1:c.289C=	ENSP00000479962.1:p.Arg97=
ENST00000621736.4:c.25C=	ENSP00000479254.1:p.Arg9=
NM_014249.3:c.289C=	NP_055064.1:p.Arg97=
NM_016346.3:c.289C=	NP_057430.1:p.Arg97=
XM_011521146.1:c.25C=	XP_011519448.1:p.Arg9=
NM_014249.4:c.289C= MANE Select	NP_055064.1:p.Arg97=
NM_016346.4:c.289C=	NP_057430.1:p.Arg97=