Canonical Allele Identifier: CA2033475789

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852834G= , CM000674.2:g.45852834G=	GRCh38
NC_000012.11:g.46246617G= , CM000674.1:g.46246617G=	GRCh37
NC_000012.10:g.44532884G=	NCBI36
NG_052800.1:g.128170G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4711G=	ENSP00000415650.3:p.Glu1571=
ENST00000457135.2:c.920G=
ENST00000334344.11:c.4711G= MANE Select	ENSP00000335044.6:p.Glu1571=
ENST00000422737.6:c.4632G=
ENST00000334344.10:c.4711G=	ENSP00000335044.6:p.Glu1571=
ENST00000422737.5:c.4264G=	ENSP00000415650.1:p.Glu1422=
ENST00000444670.5:c.3541G=	ENSP00000397307.1:p.Glu1181=
ENST00000457135.1:c.535G=	ENSP00000388357.1:p.Glu179=
ENST00000479608.5:n.4002G=
NM_152641.2:c.4711G=	NP_689854.2:p.Glu1571=
XM_006719272.2:c.4711G=	XP_006719335.1:p.Glu1571=
XM_011538025.1:c.3079G=	XP_011536327.1:p.Glu1027=
XR_944505.1:n.4859G=
NM_001347839.1:c.4711G=	NP_001334768.1:p.Glu1571=
NM_152641.3:c.4711G=	NP_689854.2:p.Glu1571=
XM_006719272.4:c.4711G=	XP_006719335.1:p.Glu1571=
XR_944505.3:n.4842G=
NM_152641.4:c.4711G= MANE Select	NP_689854.2:p.Glu1571=
NM_001347839.2:c.4711G=	NP_001334768.1:p.Glu1571=