Canonical Allele Identifier: CA2033475744

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852714C= , CM000674.2:g.45852714C=	GRCh38
NC_000012.11:g.46246497C= , CM000674.1:g.46246497C=	GRCh37
NC_000012.10:g.44532764C=	NCBI36
NG_052800.1:g.128050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4591C=	ENSP00000415650.3:p.Pro1531=
ENST00000457135.2:c.800C=
ENST00000334344.11:c.4591C= MANE Select	ENSP00000335044.6:p.Pro1531=
ENST00000422737.6:c.4512C=
ENST00000334344.10:c.4591C=	ENSP00000335044.6:p.Pro1531=
ENST00000422737.5:c.4144C=	ENSP00000415650.1:p.Pro1382=
ENST00000444670.5:c.3421C=	ENSP00000397307.1:p.Pro1141=
ENST00000457135.1:c.415C=	ENSP00000388357.1:p.Pro139=
ENST00000479608.5:n.3882C=
NM_152641.2:c.4591C=	NP_689854.2:p.Pro1531=
XM_006719272.2:c.4591C=	XP_006719335.1:p.Pro1531=
XM_011538025.1:c.2959C=	XP_011536327.1:p.Pro987=
XR_944505.1:n.4739C=
NM_001347839.1:c.4591C=	NP_001334768.1:p.Pro1531=
NM_152641.3:c.4591C=	NP_689854.2:p.Pro1531=
XM_006719272.4:c.4591C=	XP_006719335.1:p.Pro1531=
XR_944505.3:n.4722C=
NM_152641.4:c.4591C= MANE Select	NP_689854.2:p.Pro1531=
NM_001347839.2:c.4591C=	NP_001334768.1:p.Pro1531=