Canonical Allele Identifier: CA1160180731
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696694G= , CM000663.2:g.26696694G= GRCh38
NC_000001.10:g.27023185G= , CM000663.1:g.27023185G= GRCh37
NC_000001.9:g.26895772G= NCBI36
NG_029965.1:g.5664G= , LRG_875:g.5664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.291G= MANE Select ENSP00000320485.7:p.Glu97=
ENST00000430799.7:c.-13+3077G= ENSP00000390317.3:n.-13+3077G=
ENST00000637465.1:c.-13+594G= ENSP00000490650.1:n.-13+594G=
ENST00000324856.11:c.291G= ENSP00000320485.7:p.Glu97=
ENST00000457599.6:c.291G= ENSP00000387636.2:p.Glu97=
NM_006015.4:c.291G= , LRG_875t1:c.291G= NP_006006.3:p.Glu97=
NM_139135.2:c.291G= NP_624361.1:p.Glu97=
NM_006015.5:c.291G= NP_006006.3:p.Glu97=
NM_139135.3:c.291G= NP_624361.1:p.Glu97=
NM_006015.6:c.291G= MANE Select NP_006006.3:p.Glu97=
NM_139135.4:c.291G= NP_624361.1:p.Glu97=