Canonical Allele Identifier: CA2033475675

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852567C= , CM000674.2:g.45852567C=	GRCh38
NC_000012.11:g.46246350C= , CM000674.1:g.46246350C=	GRCh37
NC_000012.10:g.44532617C=	NCBI36
NG_052800.1:g.127903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4444C=	ENSP00000415650.3:p.Gln1482=
ENST00000457135.2:c.653C=
ENST00000334344.11:c.4444C= MANE Select	ENSP00000335044.6:p.Gln1482=
ENST00000422737.6:c.4365C=
ENST00000334344.10:c.4444C=	ENSP00000335044.6:p.Gln1482=
ENST00000422737.5:c.3997C=	ENSP00000415650.1:p.Gln1333=
ENST00000444670.5:c.3274C=	ENSP00000397307.1:p.Gln1092=
ENST00000457135.1:c.268C=	ENSP00000388357.1:p.Gln90=
ENST00000479608.5:n.3735C=
NM_152641.2:c.4444C=	NP_689854.2:p.Gln1482=
XM_006719272.2:c.4444C=	XP_006719335.1:p.Gln1482=
XM_011538025.1:c.2812C=	XP_011536327.1:p.Gln938=
XR_944505.1:n.4592C=
NM_001347839.1:c.4444C=	NP_001334768.1:p.Gln1482=
NM_152641.3:c.4444C=	NP_689854.2:p.Gln1482=
XM_006719272.4:c.4444C=	XP_006719335.1:p.Gln1482=
XR_944505.3:n.4575C=
NM_152641.4:c.4444C= MANE Select	NP_689854.2:p.Gln1482=
NM_001347839.2:c.4444C=	NP_001334768.1:p.Gln1482=