Canonical Allele Identifier: CA645513078
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696814_26696817del , CM000663.2:g.26696814_26696817del GRCh38
NC_000001.10:g.27023305_27023308del , CM000663.1:g.27023305_27023308del GRCh37
NC_000001.9:g.26895892_26895895del NCBI36
NG_029965.1:g.5784_5787del , LRG_875:g.5784_5787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.411_414del MANE Select ENSP00000320485.7:p.His137GlnfsTer?
ENST00000430799.7:c.-13+3197_-13+3200del ENSP00000390317.3:n.-13+3197_-13+3200del
ENST00000637465.1:c.-13+714_-13+717del ENSP00000490650.1:n.-13+714_-13+717del
ENST00000324856.11:c.411_414del ENSP00000320485.7:p.His137GlnfsTer?
ENST00000457599.6:c.411_414del ENSP00000387636.2:p.His137GlnfsTer?
NM_006015.4:c.411_414del , LRG_875t1:c.411_414del NP_006006.3:p.His137GlnfsTer?
NM_139135.2:c.411_414del NP_624361.1:p.His137GlnfsTer?
NM_006015.5:c.411_414del NP_006006.3:p.His137GlnfsTer?
NM_139135.3:c.411_414del NP_624361.1:p.His137GlnfsTer?
NM_006015.6:c.411_414del MANE Select NP_006006.3:p.His137GlnfsTer?
NM_139135.4:c.411_414del NP_624361.1:p.His137GlnfsTer?