Canonical Allele Identifier: CA1143836186

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779170C= , CM000663.2:g.26779170C=	GRCh38
NC_000001.10:g.27105661C= , CM000663.1:g.27105661C=	GRCh37
NC_000001.9:g.26978248C=	NCBI36
NG_029965.1:g.88140C= , LRG_875:g.88140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5272C= MANE Select	ENSP00000320485.7:p.Pro1758=
ENST00000374152.7:c.4123C=	ENSP00000363267.2:p.Pro1375=
ENST00000430799.7:c.4120C=	ENSP00000390317.3:p.Pro1374=
ENST00000466382.2:c.689C=
ENST00000636219.1:c.4126C=	ENSP00000489842.1:p.Pro1376=
ENST00000637788.1:n.1072C=
ENST00000324856.11:c.5272C=	ENSP00000320485.7:p.Pro1758=
ENST00000374152.6:c.4123C=	ENSP00000363267.2:p.Pro1375=
ENST00000430799.6:c.1961C=
ENST00000457599.6:c.4621C=	ENSP00000387636.2:p.Pro1541=
ENST00000466382.1:c.689C=
ENST00000532781.1:c.770C=
NM_006015.4:c.5272C= , LRG_875t1:c.5272C=	NP_006006.3:p.Pro1758=
NM_139135.2:c.4621C=	NP_624361.1:p.Pro1541=
NM_006015.5:c.5272C=	NP_006006.3:p.Pro1758=
NM_139135.3:c.4621C=	NP_624361.1:p.Pro1541=
NM_006015.6:c.5272C= MANE Select	NP_006006.3:p.Pro1758=
NM_139135.4:c.4621C=	NP_624361.1:p.Pro1541=