Canonical Allele Identifier: CA1160218041

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779236G= , CM000663.2:g.26779236G=	GRCh38
NC_000001.10:g.27105727G= , CM000663.1:g.27105727G=	GRCh37
NC_000001.9:g.26978314G=	NCBI36
NG_029965.1:g.88206G= , LRG_875:g.88206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5338G= MANE Select	ENSP00000320485.7:p.Glu1780=
ENST00000374152.7:c.4189G=	ENSP00000363267.2:p.Glu1397=
ENST00000430799.7:c.4186G=	ENSP00000390317.3:p.Glu1396=
ENST00000466382.2:c.755G=
ENST00000636219.1:c.4192G=	ENSP00000489842.1:p.Glu1398=
ENST00000637788.1:n.1138G=
ENST00000324856.11:c.5338G=	ENSP00000320485.7:p.Glu1780=
ENST00000374152.6:c.4189G=	ENSP00000363267.2:p.Glu1397=
ENST00000430799.6:c.2027G=
ENST00000457599.6:c.4687G=	ENSP00000387636.2:p.Glu1563=
ENST00000466382.1:c.755G=
ENST00000532781.1:c.836G=
NM_006015.4:c.5338G= , LRG_875t1:c.5338G=	NP_006006.3:p.Glu1780=
NM_139135.2:c.4687G=	NP_624361.1:p.Glu1563=
NM_006015.5:c.5338G=	NP_006006.3:p.Glu1780=
NM_139135.3:c.4687G=	NP_624361.1:p.Glu1563=
NM_006015.6:c.5338G= MANE Select	NP_006006.3:p.Glu1780=
NM_139135.4:c.4687G=	NP_624361.1:p.Glu1563=