Canonical Allele Identifier: CA2033475767

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852773C= , CM000674.2:g.45852773C=	GRCh38
NC_000012.11:g.46246556C= , CM000674.1:g.46246556C=	GRCh37
NC_000012.10:g.44532823C=	NCBI36
NG_052800.1:g.128109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4650C=	ENSP00000415650.3:p.Ser1550=
ENST00000457135.2:c.859C=
ENST00000334344.11:c.4650C= MANE Select	ENSP00000335044.6:p.Ser1550=
ENST00000422737.6:c.4571C=
ENST00000334344.10:c.4650C=	ENSP00000335044.6:p.Ser1550=
ENST00000422737.5:c.4203C=	ENSP00000415650.1:p.Ser1401=
ENST00000444670.5:c.3480C=	ENSP00000397307.1:p.Ser1160=
ENST00000457135.1:c.474C=	ENSP00000388357.1:p.Ser158=
ENST00000479608.5:n.3941C=
NM_152641.2:c.4650C=	NP_689854.2:p.Ser1550=
XM_006719272.2:c.4650C=	XP_006719335.1:p.Ser1550=
XM_011538025.1:c.3018C=	XP_011536327.1:p.Ser1006=
XR_944505.1:n.4798C=
NM_001347839.1:c.4650C=	NP_001334768.1:p.Ser1550=
NM_152641.3:c.4650C=	NP_689854.2:p.Ser1550=
XM_006719272.4:c.4650C=	XP_006719335.1:p.Ser1550=
XR_944505.3:n.4781C=
NM_152641.4:c.4650C= MANE Select	NP_689854.2:p.Ser1550=
NM_001347839.2:c.4650C=	NP_001334768.1:p.Ser1550=