Canonical Allele Identifier: CA2629291546
Gene: NR2E3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000617575.5:c.129del MANE Select ENSP00000482504.1:p.Ser44ArgfsTer?
ENST00000617575.4:c.129del ENSP00000482504.1:p.Ser44ArgfsTer?
ENST00000621098.1:c.129del ENSP00000479962.1:p.Ser44ArgfsTer?
ENST00000621736.4:c.-136del ENSP00000479254.1:n.-136del
NM_014249.3:c.129del NP_055064.1:p.Ser44ArgfsTer?
NM_016346.3:c.129del NP_057430.1:p.Ser44ArgfsTer?
XM_011521146.1:c.-136del XP_011519448.1:n.-136del
NM_014249.4:c.129del MANE Select NP_055064.1:p.Ser44ArgfsTer?
NM_016346.4:c.129del NP_057430.1:p.Ser44ArgfsTer?