Canonical Allele Identifier: CA1160218020
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779185G= , CM000663.2:g.26779185G= GRCh38
NC_000001.10:g.27105676G= , CM000663.1:g.27105676G= GRCh37
NC_000001.9:g.26978263G= NCBI36
NG_029965.1:g.88155G= , LRG_875:g.88155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.5287G= MANE Select ENSP00000320485.7:p.Glu1763=
ENST00000374152.7:c.4138G= ENSP00000363267.2:p.Glu1380=
ENST00000430799.7:c.4135G= ENSP00000390317.3:p.Glu1379=
ENST00000466382.2:c.704G=
ENST00000636219.1:c.4141G= ENSP00000489842.1:p.Glu1381=
ENST00000637788.1:n.1087G=
ENST00000324856.11:c.5287G= ENSP00000320485.7:p.Glu1763=
ENST00000374152.6:c.4138G= ENSP00000363267.2:p.Glu1380=
ENST00000430799.6:c.1976G=
ENST00000457599.6:c.4636G= ENSP00000387636.2:p.Glu1546=
ENST00000466382.1:c.704G=
ENST00000532781.1:c.785G=
NM_006015.4:c.5287G= , LRG_875t1:c.5287G= NP_006006.3:p.Glu1763=
NM_139135.2:c.4636G= NP_624361.1:p.Glu1546=
NM_006015.5:c.5287G= NP_006006.3:p.Glu1763=
NM_139135.3:c.4636G= NP_624361.1:p.Glu1546=
NM_006015.6:c.5287G= MANE Select NP_006006.3:p.Glu1763=
NM_139135.4:c.4636G= NP_624361.1:p.Glu1546=