Canonical Allele Identifier: CA2033475777

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852793C= , CM000674.2:g.45852793C=	GRCh38
NC_000012.11:g.46246576C= , CM000674.1:g.46246576C=	GRCh37
NC_000012.10:g.44532843C=	NCBI36
NG_052800.1:g.128129C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4670C=	ENSP00000415650.3:p.Pro1557=
ENST00000457135.2:c.879C=
ENST00000334344.11:c.4670C= MANE Select	ENSP00000335044.6:p.Pro1557=
ENST00000422737.6:c.4591C=
ENST00000334344.10:c.4670C=	ENSP00000335044.6:p.Pro1557=
ENST00000422737.5:c.4223C=	ENSP00000415650.1:p.Pro1408=
ENST00000444670.5:c.3500C=	ENSP00000397307.1:p.Pro1167=
ENST00000457135.1:c.494C=	ENSP00000388357.1:p.Pro165=
ENST00000479608.5:n.3961C=
NM_152641.2:c.4670C=	NP_689854.2:p.Pro1557=
XM_006719272.2:c.4670C=	XP_006719335.1:p.Pro1557=
XM_011538025.1:c.3038C=	XP_011536327.1:p.Pro1013=
XR_944505.1:n.4818C=
NM_001347839.1:c.4670C=	NP_001334768.1:p.Pro1557=
NM_152641.3:c.4670C=	NP_689854.2:p.Pro1557=
XM_006719272.4:c.4670C=	XP_006719335.1:p.Pro1557=
XR_944505.3:n.4801C=
NM_152641.4:c.4670C= MANE Select	NP_689854.2:p.Pro1557=
NM_001347839.2:c.4670C=	NP_001334768.1:p.Pro1557=