Canonical Allele Identifier: CA2629291504
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71811454_71811455insCGGCC , CM000677.2:g.71811454_71811455insCGGCC GRCh38
NC_000015.9:g.72103794_72103795insCGGCC , CM000677.1:g.72103794_72103795insCGGCC GRCh37
NC_000015.8:g.69890848_69890849insCGGCC NCBI36
NG_009113.2:g.5900_5901insCGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000617575.5:c.119-29_119-28insCGGCC MANE Select ENSP00000482504.1:n.119-29_119-28insCGGCC
ENST00000617575.4:c.119-29_119-28insCGGCC ENSP00000482504.1:n.119-29_119-28insCGGCC
ENST00000621098.1:c.119-29_119-28insCGGCC ENSP00000479962.1:n.119-29_119-28insCGGCC
ENST00000621736.4:c.-146-29_-146-28insCGGCC ENSP00000479254.1:n.-146-29_-146-28insCGGCC
NM_014249.3:c.119-29_119-28insCGGCC NP_055064.1:n.119-29_119-28insCGGCC
NM_016346.3:c.119-29_119-28insCGGCC NP_057430.1:n.119-29_119-28insCGGCC
XM_011521146.1:c.-146-29_-146-28insCGGCC XP_011519448.1:n.-146-29_-146-28insCGGCC
NM_014249.4:c.119-29_119-28insCGGCC MANE Select NP_055064.1:n.119-29_119-28insCGGCC
NM_016346.4:c.119-29_119-28insCGGCC NP_057430.1:n.119-29_119-28insCGGCC