Canonical Allele Identifier: CA1160218050

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779260A= , CM000663.2:g.26779260A=	GRCh38
NC_000001.10:g.27105751A= , CM000663.1:g.27105751A=	GRCh37
NC_000001.9:g.26978338A=	NCBI36
NG_029965.1:g.88230A= , LRG_875:g.88230A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5362A= MANE Select	ENSP00000320485.7:p.Ile1788=
ENST00000374152.7:c.4213A=	ENSP00000363267.2:p.Ile1405=
ENST00000430799.7:c.4210A=	ENSP00000390317.3:p.Ile1404=
ENST00000466382.2:c.779A=
ENST00000636219.1:c.4216A=	ENSP00000489842.1:p.Ile1406=
ENST00000637788.1:n.1162A=
ENST00000324856.11:c.5362A=	ENSP00000320485.7:p.Ile1788=
ENST00000374152.6:c.4213A=	ENSP00000363267.2:p.Ile1405=
ENST00000430799.6:c.2051A=
ENST00000457599.6:c.4711A=	ENSP00000387636.2:p.Ile1571=
ENST00000466382.1:c.779A=
ENST00000532781.1:c.860A=
NM_006015.4:c.5362A= , LRG_875t1:c.5362A=	NP_006006.3:p.Ile1788=
NM_139135.2:c.4711A=	NP_624361.1:p.Ile1571=
NM_006015.5:c.5362A=	NP_006006.3:p.Ile1788=
NM_139135.3:c.4711A=	NP_624361.1:p.Ile1571=
NM_006015.6:c.5362A= MANE Select	NP_006006.3:p.Ile1788=
NM_139135.4:c.4711A=	NP_624361.1:p.Ile1571=