Canonical Allele Identifier: CA1160180787
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696772_26696778delinsCGGCGGT , CM000663.2:g.26696772_26696778delinsCGGCGGT GRCh38
NC_000001.10:g.27023263_27023269delinsCGGCGGT , CM000663.1:g.27023263_27023269delinsCGGCGGT GRCh37
NC_000001.9:g.26895850_26895856delinsCGGCGGT NCBI36
NG_029965.1:g.5742_5748delinsCGGCGGT , LRG_875:g.5742_5748delinsCGGCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.369_375delinsCGGCGGT MANE Select ENSP00000320485.7:p.Gly123=
ENST00000430799.7:c.-13+3155_-13+3161delinsCGGCGGT ENSP00000390317.3:n.-13+3155_-13+3161delinsCGGCGGT
ENST00000637465.1:c.-13+672_-13+678delinsCGGCGGT ENSP00000490650.1:n.-13+672_-13+678delinsCGGCGGT
ENST00000324856.11:c.369_375delinsCGGCGGT ENSP00000320485.7:p.Gly123=
ENST00000457599.6:c.369_375delinsCGGCGGT ENSP00000387636.2:p.Gly123=
NM_006015.4:c.369_375delinsCGGCGGT , LRG_875t1:c.369_375delinsCGGCGGT NP_006006.3:p.Gly123=
NM_139135.2:c.369_375delinsCGGCGGT NP_624361.1:p.Gly123=
NM_006015.5:c.369_375delinsCGGCGGT NP_006006.3:p.Gly123=
NM_139135.3:c.369_375delinsCGGCGGT NP_624361.1:p.Gly123=
NM_006015.6:c.369_375delinsCGGCGGT MANE Select NP_006006.3:p.Gly123=
NM_139135.4:c.369_375delinsCGGCGGT NP_624361.1:p.Gly123=