Canonical Allele Identifier: CA2033475782

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852815T= , CM000674.2:g.45852815T=	GRCh38
NC_000012.11:g.46246598T= , CM000674.1:g.46246598T=	GRCh37
NC_000012.10:g.44532865T=	NCBI36
NG_052800.1:g.128151T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4692T=	ENSP00000415650.3:p.Thr1564=
ENST00000457135.2:c.901T=
ENST00000334344.11:c.4692T= MANE Select	ENSP00000335044.6:p.Thr1564=
ENST00000422737.6:c.4613T=
ENST00000334344.10:c.4692T=	ENSP00000335044.6:p.Thr1564=
ENST00000422737.5:c.4245T=	ENSP00000415650.1:p.Thr1415=
ENST00000444670.5:c.3522T=	ENSP00000397307.1:p.Thr1174=
ENST00000457135.1:c.516T=	ENSP00000388357.1:p.Thr172=
ENST00000479608.5:n.3983T=
NM_152641.2:c.4692T=	NP_689854.2:p.Thr1564=
XM_006719272.2:c.4692T=	XP_006719335.1:p.Thr1564=
XM_011538025.1:c.3060T=	XP_011536327.1:p.Thr1020=
XR_944505.1:n.4840T=
NM_001347839.1:c.4692T=	NP_001334768.1:p.Thr1564=
NM_152641.3:c.4692T=	NP_689854.2:p.Thr1564=
XM_006719272.4:c.4692T=	XP_006719335.1:p.Thr1564=
XR_944505.3:n.4823T=
NM_152641.4:c.4692T= MANE Select	NP_689854.2:p.Thr1564=
NM_001347839.2:c.4692T=	NP_001334768.1:p.Thr1564=