Canonical Allele Identifier: CA2644294104
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696677_26696678del , CM000663.2:g.26696677_26696678del GRCh38
NC_000001.10:g.27023168_27023169del , CM000663.1:g.27023168_27023169del GRCh37
NC_000001.9:g.26895755_26895756del NCBI36
NG_029965.1:g.5647_5648del , LRG_875:g.5647_5648del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.274_275del MANE Select ENSP00000320485.7:p.Gly92ArgfsTer18
ENST00000430799.7:c.-13+3060_-13+3061del ENSP00000390317.3:n.-13+3060_-13+3061del
ENST00000637465.1:c.-13+577_-13+578del ENSP00000490650.1:n.-13+577_-13+578del
ENST00000324856.11:c.274_275del ENSP00000320485.7:p.Gly92ArgfsTer18
ENST00000457599.6:c.274_275del ENSP00000387636.2:p.Gly92ArgfsTer18
NM_006015.4:c.274_275del , LRG_875t1:c.274_275del NP_006006.3:p.Gly92ArgfsTer18
NM_139135.2:c.274_275del NP_624361.1:p.Gly92ArgfsTer18
NM_006015.5:c.274_275del NP_006006.3:p.Gly92ArgfsTer18
NM_139135.3:c.274_275del NP_624361.1:p.Gly92ArgfsTer18
NM_006015.6:c.274_275del MANE Select NP_006006.3:p.Gly92ArgfsTer18
NM_139135.4:c.274_275del NP_624361.1:p.Gly92ArgfsTer18