Canonical Allele Identifier: CA2644294109
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696684_26696685del , CM000663.2:g.26696684_26696685del GRCh38
NC_000001.10:g.27023175_27023176del , CM000663.1:g.27023175_27023176del GRCh37
NC_000001.9:g.26895762_26895763del NCBI36
NG_029965.1:g.5654_5655del , LRG_875:g.5654_5655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.281_282del MANE Select ENSP00000320485.7:p.Pro94ArgfsTer16
ENST00000430799.7:c.-13+3067_-13+3068del ENSP00000390317.3:n.-13+3067_-13+3068del
ENST00000637465.1:c.-13+584_-13+585del ENSP00000490650.1:n.-13+584_-13+585del
ENST00000324856.11:c.281_282del ENSP00000320485.7:p.Pro94ArgfsTer16
ENST00000457599.6:c.281_282del ENSP00000387636.2:p.Pro94ArgfsTer16
NM_006015.4:c.281_282del , LRG_875t1:c.281_282del NP_006006.3:p.Pro94ArgfsTer16
NM_139135.2:c.281_282del NP_624361.1:p.Pro94ArgfsTer16
NM_006015.5:c.281_282del NP_006006.3:p.Pro94ArgfsTer16
NM_139135.3:c.281_282del NP_624361.1:p.Pro94ArgfsTer16
NM_006015.6:c.281_282del MANE Select NP_006006.3:p.Pro94ArgfsTer16
NM_139135.4:c.281_282del NP_624361.1:p.Pro94ArgfsTer16