Canonical Allele Identifier: CA1160218021

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779191G= , CM000663.2:g.26779191G=	GRCh38
NC_000001.10:g.27105682G= , CM000663.1:g.27105682G=	GRCh37
NC_000001.9:g.26978269G=	NCBI36
NG_029965.1:g.88161G= , LRG_875:g.88161G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5293G= MANE Select	ENSP00000320485.7:p.Glu1765=
ENST00000374152.7:c.4144G=	ENSP00000363267.2:p.Glu1382=
ENST00000430799.7:c.4141G=	ENSP00000390317.3:p.Glu1381=
ENST00000466382.2:c.710G=
ENST00000636219.1:c.4147G=	ENSP00000489842.1:p.Glu1383=
ENST00000637788.1:n.1093G=
ENST00000324856.11:c.5293G=	ENSP00000320485.7:p.Glu1765=
ENST00000374152.6:c.4144G=	ENSP00000363267.2:p.Glu1382=
ENST00000430799.6:c.1982G=
ENST00000457599.6:c.4642G=	ENSP00000387636.2:p.Glu1548=
ENST00000466382.1:c.710G=
ENST00000532781.1:c.791G=
NM_006015.4:c.5293G= , LRG_875t1:c.5293G=	NP_006006.3:p.Glu1765=
NM_139135.2:c.4642G=	NP_624361.1:p.Glu1548=
NM_006015.5:c.5293G=	NP_006006.3:p.Glu1765=
NM_139135.3:c.4642G=	NP_624361.1:p.Glu1548=
NM_006015.6:c.5293G= MANE Select	NP_006006.3:p.Glu1765=
NM_139135.4:c.4642G=	NP_624361.1:p.Glu1548=