Canonical Allele Identifier: CA2186513440

Gene: NR2E3

Linked Data

• dbSNP Id: rs2054176612

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811306del , CM000677.2:g.71811306del	GRCh38
NC_000015.9:g.72103646del , CM000677.1:g.72103646del	GRCh37
NC_000015.8:g.69890700del	NCBI36
NG_009113.2:g.5752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.119-177del MANE Select	ENSP00000482504.1:n.119-177del
ENST00000617575.4:c.119-177del	ENSP00000482504.1:n.119-177del
ENST00000621098.1:c.119-177del	ENSP00000479962.1:n.119-177del
ENST00000621736.4:c.-146-177del	ENSP00000479254.1:n.-146-177del
NM_014249.3:c.119-177del	NP_055064.1:n.119-177del
NM_016346.3:c.119-177del	NP_057430.1:n.119-177del
XM_011521146.1:c.-146-177del	XP_011519448.1:n.-146-177del
NM_014249.4:c.119-177del MANE Select	NP_055064.1:n.119-177del
NM_016346.4:c.119-177del	NP_057430.1:n.119-177del