Canonical Allele Identifier: CA479694244
Gene: ARID2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.46246623del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852840del , CM000674.2:g.45852840del GRCh38
NC_000012.11:g.46246623del , CM000674.1:g.46246623del GRCh37
NC_000012.10:g.44532890del NCBI36
NG_052800.1:g.128176del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4717del ENSP00000415650.3:p.Ala1573LeufsTer?
ENST00000457135.2:c.926del
ENST00000334344.11:c.4717del MANE Select ENSP00000335044.6:p.Ala1573LeufsTer?
ENST00000422737.6:c.4638del
ENST00000334344.10:c.4717del ENSP00000335044.6:p.Ala1573LeufsTer?
ENST00000422737.5:c.4270del ENSP00000415650.1:p.Ala1424LeufsTer?
ENST00000444670.5:c.3547del ENSP00000397307.1:p.Ala1183LeufsTer?
ENST00000457135.1:c.541del ENSP00000388357.1:p.Ala181LeufsTer?
ENST00000479608.5:n.4008del
NM_152641.2:c.4717del NP_689854.2:p.Ala1573LeufsTer?
XM_006719272.2:c.4717del XP_006719335.1:p.Ala1573LeufsTer?
XM_011538025.1:c.3085del XP_011536327.1:p.Ala1029LeufsTer?
XR_944505.1:n.4865del
NM_001347839.1:c.4717del NP_001334768.1:p.Ala1573LeufsTer?
NM_152641.3:c.4717del NP_689854.2:p.Ala1573LeufsTer?
XM_006719272.4:c.4717del XP_006719335.1:p.Ala1573LeufsTer?
XR_944505.3:n.4848del
NM_152641.4:c.4717del MANE Select NP_689854.2:p.Ala1573LeufsTer?
NM_001347839.2:c.4717del NP_001334768.1:p.Ala1573LeufsTer?