Canonical Allele Identifier: CA2033475699

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852615G= , CM000674.2:g.45852615G=	GRCh38
NC_000012.11:g.46246398G= , CM000674.1:g.46246398G=	GRCh37
NC_000012.10:g.44532665G=	NCBI36
NG_052800.1:g.127951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4492G=	ENSP00000415650.3:p.Ala1498=
ENST00000457135.2:c.701G=
ENST00000334344.11:c.4492G= MANE Select	ENSP00000335044.6:p.Ala1498=
ENST00000422737.6:c.4413G=
ENST00000334344.10:c.4492G=	ENSP00000335044.6:p.Ala1498=
ENST00000422737.5:c.4045G=	ENSP00000415650.1:p.Ala1349=
ENST00000444670.5:c.3322G=	ENSP00000397307.1:p.Ala1108=
ENST00000457135.1:c.316G=	ENSP00000388357.1:p.Ala106=
ENST00000479608.5:n.3783G=
NM_152641.2:c.4492G=	NP_689854.2:p.Ala1498=
XM_006719272.2:c.4492G=	XP_006719335.1:p.Ala1498=
XM_011538025.1:c.2860G=	XP_011536327.1:p.Ala954=
XR_944505.1:n.4640G=
NM_001347839.1:c.4492G=	NP_001334768.1:p.Ala1498=
NM_152641.3:c.4492G=	NP_689854.2:p.Ala1498=
XM_006719272.4:c.4492G=	XP_006719335.1:p.Ala1498=
XR_944505.3:n.4623G=
NM_152641.4:c.4492G= MANE Select	NP_689854.2:p.Ala1498=
NM_001347839.2:c.4492G=	NP_001334768.1:p.Ala1498=