Canonical Allele Identifier: CA1160218000
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779151C= , CM000663.2:g.26779151C= GRCh38
NC_000001.10:g.27105642C= , CM000663.1:g.27105642C= GRCh37
NC_000001.9:g.26978229C= NCBI36
NG_029965.1:g.88121C= , LRG_875:g.88121C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5253C= MANE Select ENSP00000320485.7:p.Ser1751=
ENST00000374152.7:c.4104C= ENSP00000363267.2:p.Ser1368=
ENST00000430799.7:c.4101C= ENSP00000390317.3:p.Ser1367=
ENST00000466382.2:c.670C=
ENST00000636219.1:c.4107C= ENSP00000489842.1:p.Ser1369=
ENST00000637788.1:n.1053C=
ENST00000324856.11:c.5253C= ENSP00000320485.7:p.Ser1751=
ENST00000374152.6:c.4104C= ENSP00000363267.2:p.Ser1368=
ENST00000430799.6:c.1942C=
ENST00000457599.6:c.4602C= ENSP00000387636.2:p.Ser1534=
ENST00000466382.1:c.670C=
ENST00000532781.1:c.751C=
NM_006015.4:c.5253C= , LRG_875t1:c.5253C= NP_006006.3:p.Ser1751=
NM_139135.2:c.4602C= NP_624361.1:p.Ser1534=
NM_006015.5:c.5253C= NP_006006.3:p.Ser1751=
NM_139135.3:c.4602C= NP_624361.1:p.Ser1534=
NM_006015.6:c.5253C= MANE Select NP_006006.3:p.Ser1751=
NM_139135.4:c.4602C= NP_624361.1:p.Ser1534=