Canonical Allele Identifier: CA2033475769

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852775C= , CM000674.2:g.45852775C=	GRCh38
NC_000012.11:g.46246558C= , CM000674.1:g.46246558C=	GRCh37
NC_000012.10:g.44532825C=	NCBI36
NG_052800.1:g.128111C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4652C=	ENSP00000415650.3:p.Ala1551=
ENST00000457135.2:c.861C=
ENST00000334344.11:c.4652C= MANE Select	ENSP00000335044.6:p.Ala1551=
ENST00000422737.6:c.4573C=
ENST00000334344.10:c.4652C=	ENSP00000335044.6:p.Ala1551=
ENST00000422737.5:c.4205C=	ENSP00000415650.1:p.Ala1402=
ENST00000444670.5:c.3482C=	ENSP00000397307.1:p.Ala1161=
ENST00000457135.1:c.476C=	ENSP00000388357.1:p.Ala159=
ENST00000479608.5:n.3943C=
NM_152641.2:c.4652C=	NP_689854.2:p.Ala1551=
XM_006719272.2:c.4652C=	XP_006719335.1:p.Ala1551=
XM_011538025.1:c.3020C=	XP_011536327.1:p.Ala1007=
XR_944505.1:n.4800C=
NM_001347839.1:c.4652C=	NP_001334768.1:p.Ala1551=
NM_152641.3:c.4652C=	NP_689854.2:p.Ala1551=
XM_006719272.4:c.4652C=	XP_006719335.1:p.Ala1551=
XR_944505.3:n.4783C=
NM_152641.4:c.4652C= MANE Select	NP_689854.2:p.Ala1551=
NM_001347839.2:c.4652C=	NP_001334768.1:p.Ala1551=