Canonical Allele Identifier: CA891841747
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696668_26696684del , CM000663.2:g.26696668_26696684del GRCh38
NC_000001.10:g.27023159_27023175del , CM000663.1:g.27023159_27023175del GRCh37
NC_000001.9:g.26895746_26895762del NCBI36
NG_029965.1:g.5638_5654del , LRG_875:g.5638_5654del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.265_281del MANE Select ENSP00000320485.7:p.Gly89ArgfsTer16
ENST00000430799.7:c.-13+3051_-13+3067del ENSP00000390317.3:n.-13+3051_-13+3067del
ENST00000637465.1:c.-13+568_-13+584del ENSP00000490650.1:n.-13+568_-13+584del
ENST00000324856.11:c.265_281del ENSP00000320485.7:p.Gly89ArgfsTer16
ENST00000457599.6:c.265_281del ENSP00000387636.2:p.Gly89ArgfsTer16
NM_006015.4:c.265_281del , LRG_875t1:c.265_281del NP_006006.3:p.Gly89ArgfsTer16
NM_139135.2:c.265_281del NP_624361.1:p.Gly89ArgfsTer16
NM_006015.5:c.265_281del NP_006006.3:p.Gly89ArgfsTer16
NM_139135.3:c.265_281del NP_624361.1:p.Gly89ArgfsTer16
NM_006015.6:c.265_281del MANE Select NP_006006.3:p.Gly89ArgfsTer16
NM_139135.4:c.265_281del NP_624361.1:p.Gly89ArgfsTer16