Canonical Allele Identifier: CA1160180773
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696758G= , CM000663.2:g.26696758G= GRCh38
NC_000001.10:g.27023249G= , CM000663.1:g.27023249G= GRCh37
NC_000001.9:g.26895836G= NCBI36
NG_029965.1:g.5728G= , LRG_875:g.5728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.355G= MANE Select ENSP00000320485.7:p.Glu119=
ENST00000430799.7:c.-13+3141G= ENSP00000390317.3:n.-13+3141G=
ENST00000637465.1:c.-13+658G= ENSP00000490650.1:n.-13+658G=
ENST00000324856.11:c.355G= ENSP00000320485.7:p.Glu119=
ENST00000457599.6:c.355G= ENSP00000387636.2:p.Glu119=
NM_006015.4:c.355G= , LRG_875t1:c.355G= NP_006006.3:p.Glu119=
NM_139135.2:c.355G= NP_624361.1:p.Glu119=
NM_006015.5:c.355G= NP_006006.3:p.Glu119=
NM_139135.3:c.355G= NP_624361.1:p.Glu119=
NM_006015.6:c.355G= MANE Select NP_006006.3:p.Glu119=
NM_139135.4:c.355G= NP_624361.1:p.Glu119=