Canonical Allele Identifier: CA2033475629

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852475C= , CM000674.2:g.45852475C=	GRCh38
NC_000012.11:g.46246258C= , CM000674.1:g.46246258C=	GRCh37
NC_000012.10:g.44532525C=	NCBI36
NG_052800.1:g.127811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4352C=	ENSP00000415650.3:p.Pro1451=
ENST00000457135.2:c.561C=
ENST00000334344.11:c.4352C= MANE Select	ENSP00000335044.6:p.Pro1451=
ENST00000422737.6:c.4273C=
ENST00000334344.10:c.4352C=	ENSP00000335044.6:p.Pro1451=
ENST00000422737.5:c.3905C=	ENSP00000415650.1:p.Pro1302=
ENST00000444670.5:c.3182C=	ENSP00000397307.1:p.Pro1061=
ENST00000457135.1:c.176C=	ENSP00000388357.1:p.Pro59=
ENST00000479608.5:n.3643C=
NM_152641.2:c.4352C=	NP_689854.2:p.Pro1451=
XM_006719272.2:c.4352C=	XP_006719335.1:p.Pro1451=
XM_011538025.1:c.2720C=	XP_011536327.1:p.Pro907=
XR_944505.1:n.4500C=
NM_001347839.1:c.4352C=	NP_001334768.1:p.Pro1451=
NM_152641.3:c.4352C=	NP_689854.2:p.Pro1451=
XM_006719272.4:c.4352C=	XP_006719335.1:p.Pro1451=
XR_944505.3:n.4483C=
NM_152641.4:c.4352C= MANE Select	NP_689854.2:p.Pro1451=
NM_001347839.2:c.4352C=	NP_001334768.1:p.Pro1451=