Canonical Allele Identifier: CA2186513439

Gene: NR2E3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71811302_71811303delinsTG , CM000677.2:g.71811302_71811303delinsTG	GRCh38
NC_000015.9:g.72103642_72103643delinsTG , CM000677.1:g.72103642_72103643delinsTG	GRCh37
NC_000015.8:g.69890696_69890697delinsTG	NCBI36
NG_009113.2:g.5748_5749delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617575.5:c.119-181_119-180delinsTG MANE Select	ENSP00000482504.1:n.119-181_119-180delinsTG
ENST00000617575.4:c.119-181_119-180delinsTG	ENSP00000482504.1:n.119-181_119-180delinsTG
ENST00000621098.1:c.119-181_119-180delinsTG	ENSP00000479962.1:n.119-181_119-180delinsTG
ENST00000621736.4:c.-146-181_-146-180delinsTG	ENSP00000479254.1:n.-146-181_-146-180delinsTG
NM_014249.3:c.119-181_119-180delinsTG	NP_055064.1:n.119-181_119-180delinsTG
NM_016346.3:c.119-181_119-180delinsTG	NP_057430.1:n.119-181_119-180delinsTG
XM_011521146.1:c.-146-181_-146-180delinsTG	XP_011519448.1:n.-146-181_-146-180delinsTG
NM_014249.4:c.119-181_119-180delinsTG MANE Select	NP_055064.1:n.119-181_119-180delinsTG
NM_016346.4:c.119-181_119-180delinsTG	NP_057430.1:n.119-181_119-180delinsTG