Canonical Allele Identifier: CA2644294121
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696742del , CM000663.2:g.26696742del GRCh38
NC_000001.10:g.27023233del , CM000663.1:g.27023233del GRCh37
NC_000001.9:g.26895820del NCBI36
NG_029965.1:g.5712del , LRG_875:g.5712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.339del MANE Select ENSP00000320485.7:p.Asn114ThrfsTer?
ENST00000430799.7:c.-13+3125del ENSP00000390317.3:n.-13+3125del
ENST00000637465.1:c.-13+642del ENSP00000490650.1:n.-13+642del
ENST00000324856.11:c.339del ENSP00000320485.7:p.Asn114ThrfsTer?
ENST00000457599.6:c.339del ENSP00000387636.2:p.Asn114ThrfsTer?
NM_006015.4:c.339del , LRG_875t1:c.339del NP_006006.3:p.Asn114ThrfsTer?
NM_139135.2:c.339del NP_624361.1:p.Asn114ThrfsTer?
NM_006015.5:c.339del NP_006006.3:p.Asn114ThrfsTer?
NM_139135.3:c.339del NP_624361.1:p.Asn114ThrfsTer?
NM_006015.6:c.339del MANE Select NP_006006.3:p.Asn114ThrfsTer?
NM_139135.4:c.339del NP_624361.1:p.Asn114ThrfsTer?