Canonical Allele Identifier: CA1160218013

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779175G= , CM000663.2:g.26779175G=	GRCh38
NC_000001.10:g.27105666G= , CM000663.1:g.27105666G=	GRCh37
NC_000001.9:g.26978253G=	NCBI36
NG_029965.1:g.88145G= , LRG_875:g.88145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5277G= MANE Select	ENSP00000320485.7:p.Met1759=
ENST00000374152.7:c.4128G=	ENSP00000363267.2:p.Met1376=
ENST00000430799.7:c.4125G=	ENSP00000390317.3:p.Met1375=
ENST00000466382.2:c.694G=
ENST00000636219.1:c.4131G=	ENSP00000489842.1:p.Met1377=
ENST00000637788.1:n.1077G=
ENST00000324856.11:c.5277G=	ENSP00000320485.7:p.Met1759=
ENST00000374152.6:c.4128G=	ENSP00000363267.2:p.Met1376=
ENST00000430799.6:c.1966G=
ENST00000457599.6:c.4626G=	ENSP00000387636.2:p.Met1542=
ENST00000466382.1:c.694G=
ENST00000532781.1:c.775G=
NM_006015.4:c.5277G= , LRG_875t1:c.5277G=	NP_006006.3:p.Met1759=
NM_139135.2:c.4626G=	NP_624361.1:p.Met1542=
NM_006015.5:c.5277G=	NP_006006.3:p.Met1759=
NM_139135.3:c.4626G=	NP_624361.1:p.Met1542=
NM_006015.6:c.5277G= MANE Select	NP_006006.3:p.Met1759=
NM_139135.4:c.4626G=	NP_624361.1:p.Met1542=