Canonical Allele Identifier: CA2739291636
Gene: ARID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852826dup , CM000674.2:g.45852826dup GRCh38
NC_000012.11:g.46246609dup , CM000674.1:g.46246609dup GRCh37
NC_000012.10:g.44532876dup NCBI36
NG_052800.1:g.128162dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4703dup ENSP00000415650.3:p.Ala1569SerfsTer?
ENST00000457135.2:c.912dup
ENST00000334344.11:c.4703dup MANE Select ENSP00000335044.6:p.Ala1569SerfsTer?
ENST00000422737.6:c.4624dup
ENST00000334344.10:c.4703dup ENSP00000335044.6:p.Ala1569SerfsTer?
ENST00000422737.5:c.4256dup ENSP00000415650.1:p.Ala1420SerfsTer?
ENST00000444670.5:c.3533dup ENSP00000397307.1:p.Ala1179SerfsTer?
ENST00000457135.1:c.527dup ENSP00000388357.1:p.Ala177SerfsTer?
ENST00000479608.5:n.3994dup
NM_152641.2:c.4703dup NP_689854.2:p.Ala1569SerfsTer?
XM_006719272.2:c.4703dup XP_006719335.1:p.Ala1569SerfsTer?
XM_011538025.1:c.3071dup XP_011536327.1:p.Ala1025SerfsTer?
XR_944505.1:n.4851dup
NM_001347839.1:c.4703dup NP_001334768.1:p.Ala1569SerfsTer?
NM_152641.3:c.4703dup NP_689854.2:p.Ala1569SerfsTer?
XM_006719272.4:c.4703dup XP_006719335.1:p.Ala1569SerfsTer?
XR_944505.3:n.4834dup
NM_152641.4:c.4703dup MANE Select NP_689854.2:p.Ala1569SerfsTer?
NM_001347839.2:c.4703dup NP_001334768.1:p.Ala1569SerfsTer?