Canonical Allele Identifier: CA1160218031
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779205A= , CM000663.2:g.26779205A= GRCh38
NC_000001.10:g.27105696A= , CM000663.1:g.27105696A= GRCh37
NC_000001.9:g.26978283A= NCBI36
NG_029965.1:g.88175A= , LRG_875:g.88175A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.5307A= MANE Select ENSP00000320485.7:p.Leu1769=
ENST00000374152.7:c.4158A= ENSP00000363267.2:p.Leu1386=
ENST00000430799.7:c.4155A= ENSP00000390317.3:p.Leu1385=
ENST00000466382.2:c.724A=
ENST00000636219.1:c.4161A= ENSP00000489842.1:p.Leu1387=
ENST00000637788.1:n.1107A=
ENST00000324856.11:c.5307A= ENSP00000320485.7:p.Leu1769=
ENST00000374152.6:c.4158A= ENSP00000363267.2:p.Leu1386=
ENST00000430799.6:c.1996A=
ENST00000457599.6:c.4656A= ENSP00000387636.2:p.Leu1552=
ENST00000466382.1:c.724A=
ENST00000532781.1:c.805A=
NM_006015.4:c.5307A= , LRG_875t1:c.5307A= NP_006006.3:p.Leu1769=
NM_139135.2:c.4656A= NP_624361.1:p.Leu1552=
NM_006015.5:c.5307A= NP_006006.3:p.Leu1769=
NM_139135.3:c.4656A= NP_624361.1:p.Leu1552=
NM_006015.6:c.5307A= MANE Select NP_006006.3:p.Leu1769=
NM_139135.4:c.4656A= NP_624361.1:p.Leu1552=