Canonical Allele Identifier: CA2618443423

Gene: ARID2

Linked Data

• gnomAD v4: 12-45852833-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852834del , CM000674.2:g.45852834del	GRCh38
NC_000012.11:g.46246617del , CM000674.1:g.46246617del	GRCh37
NC_000012.10:g.44532884del	NCBI36
NG_052800.1:g.128170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4711del	ENSP00000415650.3:p.Glu1571LysfsTer?
ENST00000457135.2:c.920del
ENST00000334344.11:c.4711del MANE Select	ENSP00000335044.6:p.Glu1571LysfsTer?
ENST00000422737.6:c.4632del
ENST00000334344.10:c.4711del	ENSP00000335044.6:p.Glu1571LysfsTer?
ENST00000422737.5:c.4264del	ENSP00000415650.1:p.Glu1422LysfsTer?
ENST00000444670.5:c.3541del	ENSP00000397307.1:p.Glu1181LysfsTer?
ENST00000457135.1:c.535del	ENSP00000388357.1:p.Glu179LysfsTer?
ENST00000479608.5:n.4002del
NM_152641.2:c.4711del	NP_689854.2:p.Glu1571LysfsTer?
XM_006719272.2:c.4711del	XP_006719335.1:p.Glu1571LysfsTer?
XM_011538025.1:c.3079del	XP_011536327.1:p.Glu1027LysfsTer?
XR_944505.1:n.4859del
NM_001347839.1:c.4711del	NP_001334768.1:p.Glu1571LysfsTer?
NM_152641.3:c.4711del	NP_689854.2:p.Glu1571LysfsTer?
XM_006719272.4:c.4711del	XP_006719335.1:p.Glu1571LysfsTer?
XR_944505.3:n.4842del
NM_152641.4:c.4711del MANE Select	NP_689854.2:p.Glu1571LysfsTer?
NM_001347839.2:c.4711del	NP_001334768.1:p.Glu1571LysfsTer?