Canonical Allele Identifier: CA2186513442

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811308G= , CM000677.2:g.71811308G=	GRCh38
NC_000015.9:g.72103648G= , CM000677.1:g.72103648G=	GRCh37
NC_000015.8:g.69890702G=	NCBI36
NG_009113.2:g.5754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.119-175G= MANE Select	ENSP00000482504.1:n.119-175G=
ENST00000617575.4:c.119-175G=	ENSP00000482504.1:n.119-175G=
ENST00000621098.1:c.119-175G=	ENSP00000479962.1:n.119-175G=
ENST00000621736.4:c.-146-175G=	ENSP00000479254.1:n.-146-175G=
NM_014249.3:c.119-175G=	NP_055064.1:n.119-175G=
NM_016346.3:c.119-175G=	NP_057430.1:n.119-175G=
XM_011521146.1:c.-146-175G=	XP_011519448.1:n.-146-175G=
NM_014249.4:c.119-175G= MANE Select	NP_055064.1:n.119-175G=
NM_016346.4:c.119-175G=	NP_057430.1:n.119-175G=