Canonical Allele Identifier: CA2695216574
Gene: ARID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852810_45852813dup , CM000674.2:g.45852810_45852813dup GRCh38
NC_000012.11:g.46246593_46246596dup , CM000674.1:g.46246593_46246596dup GRCh37
NC_000012.10:g.44532860_44532863dup NCBI36
NG_052800.1:g.128146_128149dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4687_4690dup ENSP00000415650.3:p.Thr1564LysfsTer5
ENST00000457135.2:c.896_899dup
ENST00000334344.11:c.4687_4690dup MANE Select ENSP00000335044.6:p.Thr1564LysfsTer5
ENST00000422737.6:c.4608_4611dup
ENST00000334344.10:c.4687_4690dup ENSP00000335044.6:p.Thr1564LysfsTer5
ENST00000422737.5:c.4240_4243dup ENSP00000415650.1:p.Thr1415LysfsTer5
ENST00000444670.5:c.3517_3520dup ENSP00000397307.1:p.Thr1174LysfsTer5
ENST00000457135.1:c.511_514dup ENSP00000388357.1:p.Thr172LysfsTer5
ENST00000479608.5:n.3978_3981dup
NM_152641.2:c.4687_4690dup NP_689854.2:p.Thr1564LysfsTer5
XM_006719272.2:c.4687_4690dup XP_006719335.1:p.Thr1564LysfsTer5
XM_011538025.1:c.3055_3058dup XP_011536327.1:p.Thr1020LysfsTer5
XR_944505.1:n.4835_4838dup
NM_001347839.1:c.4687_4690dup NP_001334768.1:p.Thr1564LysfsTer5
NM_152641.3:c.4687_4690dup NP_689854.2:p.Thr1564LysfsTer5
XM_006719272.4:c.4687_4690dup XP_006719335.1:p.Thr1564LysfsTer5
XR_944505.3:n.4818_4821dup
NM_152641.4:c.4687_4690dup MANE Select NP_689854.2:p.Thr1564LysfsTer5
NM_001347839.2:c.4687_4690dup NP_001334768.1:p.Thr1564LysfsTer5