Canonical Allele Identifier: CA1160218047

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779254G= , CM000663.2:g.26779254G=	GRCh38
NC_000001.10:g.27105745G= , CM000663.1:g.27105745G=	GRCh37
NC_000001.9:g.26978332G=	NCBI36
NG_029965.1:g.88224G= , LRG_875:g.88224G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5356G= MANE Select	ENSP00000320485.7:p.Glu1786=
ENST00000374152.7:c.4207G=	ENSP00000363267.2:p.Glu1403=
ENST00000430799.7:c.4204G=	ENSP00000390317.3:p.Glu1402=
ENST00000466382.2:c.773G=
ENST00000636219.1:c.4210G=	ENSP00000489842.1:p.Glu1404=
ENST00000637788.1:n.1156G=
ENST00000324856.11:c.5356G=	ENSP00000320485.7:p.Glu1786=
ENST00000374152.6:c.4207G=	ENSP00000363267.2:p.Glu1403=
ENST00000430799.6:c.2045G=
ENST00000457599.6:c.4705G=	ENSP00000387636.2:p.Glu1569=
ENST00000466382.1:c.773G=
ENST00000532781.1:c.854G=
NM_006015.4:c.5356G= , LRG_875t1:c.5356G=	NP_006006.3:p.Glu1786=
NM_139135.2:c.4705G=	NP_624361.1:p.Glu1569=
NM_006015.5:c.5356G=	NP_006006.3:p.Glu1786=
NM_139135.3:c.4705G=	NP_624361.1:p.Glu1569=
NM_006015.6:c.5356G= MANE Select	NP_006006.3:p.Glu1786=
NM_139135.4:c.4705G=	NP_624361.1:p.Glu1569=