Canonical Allele Identifier: CA1160218003

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779155G= , CM000663.2:g.26779155G=	GRCh38
NC_000001.10:g.27105646G= , CM000663.1:g.27105646G=	GRCh37
NC_000001.9:g.26978233G=	NCBI36
NG_029965.1:g.88125G= , LRG_875:g.88125G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5257G= MANE Select	ENSP00000320485.7:p.Val1753=
ENST00000374152.7:c.4108G=	ENSP00000363267.2:p.Val1370=
ENST00000430799.7:c.4105G=	ENSP00000390317.3:p.Val1369=
ENST00000466382.2:c.674G=
ENST00000636219.1:c.4111G=	ENSP00000489842.1:p.Val1371=
ENST00000637788.1:n.1057G=
ENST00000324856.11:c.5257G=	ENSP00000320485.7:p.Val1753=
ENST00000374152.6:c.4108G=	ENSP00000363267.2:p.Val1370=
ENST00000430799.6:c.1946G=
ENST00000457599.6:c.4606G=	ENSP00000387636.2:p.Val1536=
ENST00000466382.1:c.674G=
ENST00000532781.1:c.755G=
NM_006015.4:c.5257G= , LRG_875t1:c.5257G=	NP_006006.3:p.Val1753=
NM_139135.2:c.4606G=	NP_624361.1:p.Val1536=
NM_006015.5:c.5257G=	NP_006006.3:p.Val1753=
NM_139135.3:c.4606G=	NP_624361.1:p.Val1536=
NM_006015.6:c.5257G= MANE Select	NP_006006.3:p.Val1753=
NM_139135.4:c.4606G=	NP_624361.1:p.Val1536=