Canonical Allele Identifier: CA1160218001
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779152A= , CM000663.2:g.26779152A= GRCh38
NC_000001.10:g.27105643A= , CM000663.1:g.27105643A= GRCh37
NC_000001.9:g.26978230A= NCBI36
NG_029965.1:g.88122A= , LRG_875:g.88122A=

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5254A= MANE Select ENSP00000320485.7:p.Lys1752=
ENST00000374152.7:c.4105A= ENSP00000363267.2:p.Lys1369=
ENST00000430799.7:c.4102A= ENSP00000390317.3:p.Lys1368=
ENST00000466382.2:c.671A=
ENST00000636219.1:c.4108A= ENSP00000489842.1:p.Lys1370=
ENST00000637788.1:n.1054A=
ENST00000324856.11:c.5254A= ENSP00000320485.7:p.Lys1752=
ENST00000374152.6:c.4105A= ENSP00000363267.2:p.Lys1369=
ENST00000430799.6:c.1943A=
ENST00000457599.6:c.4603A= ENSP00000387636.2:p.Lys1535=
ENST00000466382.1:c.671A=
ENST00000532781.1:c.752A=
NM_006015.4:c.5254A= , LRG_875t1:c.5254A= NP_006006.3:p.Lys1752=
NM_139135.2:c.4603A= NP_624361.1:p.Lys1535=
NM_006015.5:c.5254A= NP_006006.3:p.Lys1752=
NM_139135.3:c.4603A= NP_624361.1:p.Lys1535=
NM_006015.6:c.5254A= MANE Select NP_006006.3:p.Lys1752=
NM_139135.4:c.4603A= NP_624361.1:p.Lys1535=