Canonical Allele Identifier: CA2644294090
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696669_26696682del , CM000663.2:g.26696669_26696682del GRCh38
NC_000001.10:g.27023160_27023173del , CM000663.1:g.27023160_27023173del GRCh37
NC_000001.9:g.26895747_26895760del NCBI36
NG_029965.1:g.5639_5652del , LRG_875:g.5639_5652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.266_279del MANE Select ENSP00000320485.7:p.Gly89AlafsTer17
ENST00000430799.7:c.-13+3052_-13+3065del ENSP00000390317.3:n.-13+3052_-13+3065del
ENST00000637465.1:c.-13+569_-13+582del ENSP00000490650.1:n.-13+569_-13+582del
ENST00000324856.11:c.266_279del ENSP00000320485.7:p.Gly89AlafsTer17
ENST00000457599.6:c.266_279del ENSP00000387636.2:p.Gly89AlafsTer17
NM_006015.4:c.266_279del , LRG_875t1:c.266_279del NP_006006.3:p.Gly89AlafsTer17
NM_139135.2:c.266_279del NP_624361.1:p.Gly89AlafsTer17
NM_006015.5:c.266_279del NP_006006.3:p.Gly89AlafsTer17
NM_139135.3:c.266_279del NP_624361.1:p.Gly89AlafsTer17
NM_006015.6:c.266_279del MANE Select NP_006006.3:p.Gly89AlafsTer17
NM_139135.4:c.266_279del NP_624361.1:p.Gly89AlafsTer17