Canonical Allele Identifier: CA2186513558
Gene: NR2E3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811493C= , CM000677.2:g.71811493C= GRCh38
NC_000015.9:g.72103833C= , CM000677.1:g.72103833C= GRCh37
NC_000015.8:g.69890887C= NCBI36
NG_009113.2:g.5939C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.129C= MANE Select ENSP00000482504.1:p.Pro43=
ENST00000617575.4:c.129C= ENSP00000482504.1:p.Pro43=
ENST00000621098.1:c.129C= ENSP00000479962.1:p.Pro43=
ENST00000621736.4:c.-136C= ENSP00000479254.1:n.-136C=
NM_014249.3:c.129C= NP_055064.1:p.Pro43=
NM_016346.3:c.129C= NP_057430.1:p.Pro43=
XM_011521146.1:c.-136C= XP_011519448.1:n.-136C=
NM_014249.4:c.129C= MANE Select NP_055064.1:p.Pro43=
NM_016346.4:c.129C= NP_057430.1:p.Pro43=