Canonical Allele Identifier: CA1160180771
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696756C= , CM000663.2:g.26696756C= GRCh38
NC_000001.10:g.27023247C= , CM000663.1:g.27023247C= GRCh37
NC_000001.9:g.26895834C= NCBI36
NG_029965.1:g.5726C= , LRG_875:g.5726C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.353C= MANE Select ENSP00000320485.7:p.Thr118=
ENST00000430799.7:c.-13+3139C= ENSP00000390317.3:n.-13+3139C=
ENST00000637465.1:c.-13+656C= ENSP00000490650.1:n.-13+656C=
ENST00000324856.11:c.353C= ENSP00000320485.7:p.Thr118=
ENST00000457599.6:c.353C= ENSP00000387636.2:p.Thr118=
NM_006015.4:c.353C= , LRG_875t1:c.353C= NP_006006.3:p.Thr118=
NM_139135.2:c.353C= NP_624361.1:p.Thr118=
NM_006015.5:c.353C= NP_006006.3:p.Thr118=
NM_139135.3:c.353C= NP_624361.1:p.Thr118=
NM_006015.6:c.353C= MANE Select NP_006006.3:p.Thr118=
NM_139135.4:c.353C= NP_624361.1:p.Thr118=