Canonical Allele Identifier: CA2742917359
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696528_26696663del , CM000663.2:g.26696528_26696663del GRCh38
NC_000001.10:g.27023019_27023154del , CM000663.1:g.27023019_27023154del GRCh37
NC_000001.9:g.26895606_26895741del NCBI36
NG_029965.1:g.5498_5633del , LRG_875:g.5498_5633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.125_260del MANE Select ENSP00000320485.7:p.Ala42GlufsTer14
ENST00000430799.7:c.-13+2911_-13+3046del ENSP00000390317.3:n.-13+2911_-13+3046del
ENST00000637465.1:c.-13+428_-13+563del ENSP00000490650.1:n.-13+428_-13+563del
ENST00000324856.11:c.125_260del ENSP00000320485.7:p.Ala42GlufsTer14
ENST00000457599.6:c.125_260del ENSP00000387636.2:p.Ala42GlufsTer14
NM_006015.4:c.125_260del , LRG_875t1:c.125_260del NP_006006.3:p.Ala42GlufsTer14
NM_139135.2:c.125_260del NP_624361.1:p.Ala42GlufsTer14
NM_006015.5:c.125_260del NP_006006.3:p.Ala42GlufsTer14
NM_139135.3:c.125_260del NP_624361.1:p.Ala42GlufsTer14
NM_006015.6:c.125_260del MANE Select NP_006006.3:p.Ala42GlufsTer14
NM_139135.4:c.125_260del NP_624361.1:p.Ala42GlufsTer14