Canonical Allele Identifier: CA2186513753

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811826C= , CM000677.2:g.71811826C=	GRCh38
NC_000015.9:g.72104166C= , CM000677.1:g.72104166C=	GRCh37
NC_000015.8:g.69891220C=	NCBI36
NG_009113.2:g.6272C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.306C= MANE Select	ENSP00000482504.1:p.Ala102=
ENST00000617575.4:c.306C=	ENSP00000482504.1:p.Ala102=
ENST00000621098.1:c.306C=	ENSP00000479962.1:p.Ala102=
ENST00000621736.4:c.42C=	ENSP00000479254.1:p.Ala14=
NM_014249.3:c.306C=	NP_055064.1:p.Ala102=
NM_016346.3:c.306C=	NP_057430.1:p.Ala102=
XM_011521146.1:c.42C=	XP_011519448.1:p.Ala14=
NM_014249.4:c.306C= MANE Select	NP_055064.1:p.Ala102=
NM_016346.4:c.306C=	NP_057430.1:p.Ala102=