Canonical Allele Identifier: CA2186513457

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811341_71811342delinsTG , CM000677.2:g.71811341_71811342delinsTG	GRCh38
NC_000015.9:g.72103681_72103682delinsTG , CM000677.1:g.72103681_72103682delinsTG	GRCh37
NC_000015.8:g.69890735_69890736delinsTG	NCBI36
NG_009113.2:g.5787_5788delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.119-142_119-141delinsTG MANE Select	ENSP00000482504.1:n.119-142_119-141delinsTG
ENST00000617575.4:c.119-142_119-141delinsTG	ENSP00000482504.1:n.119-142_119-141delinsTG
ENST00000621098.1:c.119-142_119-141delinsTG	ENSP00000479962.1:n.119-142_119-141delinsTG
ENST00000621736.4:c.-146-142_-146-141delinsTG	ENSP00000479254.1:n.-146-142_-146-141delinsTG
NM_014249.3:c.119-142_119-141delinsTG	NP_055064.1:n.119-142_119-141delinsTG
NM_016346.3:c.119-142_119-141delinsTG	NP_057430.1:n.119-142_119-141delinsTG
XM_011521146.1:c.-146-142_-146-141delinsTG	XP_011519448.1:n.-146-142_-146-141delinsTG
NM_014249.4:c.119-142_119-141delinsTG MANE Select	NP_055064.1:n.119-142_119-141delinsTG
NM_016346.4:c.119-142_119-141delinsTG	NP_057430.1:n.119-142_119-141delinsTG