Canonical Allele Identifier: CA2033475773

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852786G= , CM000674.2:g.45852786G=	GRCh38
NC_000012.11:g.46246569G= , CM000674.1:g.46246569G=	GRCh37
NC_000012.10:g.44532836G=	NCBI36
NG_052800.1:g.128122G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4663G=	ENSP00000415650.3:p.Ala1555=
ENST00000457135.2:c.872G=
ENST00000334344.11:c.4663G= MANE Select	ENSP00000335044.6:p.Ala1555=
ENST00000422737.6:c.4584G=
ENST00000334344.10:c.4663G=	ENSP00000335044.6:p.Ala1555=
ENST00000422737.5:c.4216G=	ENSP00000415650.1:p.Ala1406=
ENST00000444670.5:c.3493G=	ENSP00000397307.1:p.Ala1165=
ENST00000457135.1:c.487G=	ENSP00000388357.1:p.Ala163=
ENST00000479608.5:n.3954G=
NM_152641.2:c.4663G=	NP_689854.2:p.Ala1555=
XM_006719272.2:c.4663G=	XP_006719335.1:p.Ala1555=
XM_011538025.1:c.3031G=	XP_011536327.1:p.Ala1011=
XR_944505.1:n.4811G=
NM_001347839.1:c.4663G=	NP_001334768.1:p.Ala1555=
NM_152641.3:c.4663G=	NP_689854.2:p.Ala1555=
XM_006719272.4:c.4663G=	XP_006719335.1:p.Ala1555=
XR_944505.3:n.4794G=
NM_152641.4:c.4663G= MANE Select	NP_689854.2:p.Ala1555=
NM_001347839.2:c.4663G=	NP_001334768.1:p.Ala1555=