Canonical Allele Identifier: CA2695201657
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696730_26696734dup , CM000663.2:g.26696730_26696734dup GRCh38
NC_000001.10:g.27023221_27023225dup , CM000663.1:g.27023221_27023225dup GRCh37
NC_000001.9:g.26895808_26895812dup NCBI36
NG_029965.1:g.5700_5704dup , LRG_875:g.5700_5704dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.327_331dup MANE Select ENSP00000320485.7:p.Pro111LeufsTer5
ENST00000430799.7:c.-13+3113_-13+3117dup ENSP00000390317.3:n.-13+3113_-13+3117dup
ENST00000637465.1:c.-13+630_-13+634dup ENSP00000490650.1:n.-13+630_-13+634dup
ENST00000324856.11:c.327_331dup ENSP00000320485.7:p.Pro111LeufsTer5
ENST00000457599.6:c.327_331dup ENSP00000387636.2:p.Pro111LeufsTer5
NM_006015.4:c.327_331dup , LRG_875t1:c.327_331dup NP_006006.3:p.Pro111LeufsTer5
NM_139135.2:c.327_331dup NP_624361.1:p.Pro111LeufsTer5
NM_006015.5:c.327_331dup NP_006006.3:p.Pro111LeufsTer5
NM_139135.3:c.327_331dup NP_624361.1:p.Pro111LeufsTer5
NM_006015.6:c.327_331dup MANE Select NP_006006.3:p.Pro111LeufsTer5
NM_139135.4:c.327_331dup NP_624361.1:p.Pro111LeufsTer5