Canonical Allele Identifier: CA1160218039

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779222A= , CM000663.2:g.26779222A=	GRCh38
NC_000001.10:g.27105713A= , CM000663.1:g.27105713A=	GRCh37
NC_000001.9:g.26978300A=	NCBI36
NG_029965.1:g.88192A= , LRG_875:g.88192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5324A= MANE Select	ENSP00000320485.7:p.Glu1775=
ENST00000374152.7:c.4175A=	ENSP00000363267.2:p.Glu1392=
ENST00000430799.7:c.4172A=	ENSP00000390317.3:p.Glu1391=
ENST00000466382.2:c.741A=
ENST00000636219.1:c.4178A=	ENSP00000489842.1:p.Glu1393=
ENST00000637788.1:n.1124A=
ENST00000324856.11:c.5324A=	ENSP00000320485.7:p.Glu1775=
ENST00000374152.6:c.4175A=	ENSP00000363267.2:p.Glu1392=
ENST00000430799.6:c.2013A=
ENST00000457599.6:c.4673A=	ENSP00000387636.2:p.Glu1558=
ENST00000466382.1:c.741A=
ENST00000532781.1:c.822A=
NM_006015.4:c.5324A= , LRG_875t1:c.5324A=	NP_006006.3:p.Glu1775=
NM_139135.2:c.4673A=	NP_624361.1:p.Glu1558=
NM_006015.5:c.5324A=	NP_006006.3:p.Glu1775=
NM_139135.3:c.4673A=	NP_624361.1:p.Glu1558=
NM_006015.6:c.5324A= MANE Select	NP_006006.3:p.Glu1775=
NM_139135.4:c.4673A=	NP_624361.1:p.Glu1558=