Canonical Allele Identifier: CA1160180712
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696665_26696683delinsGCCGGCAGCGGCGGCGGGC , CM000663.2:g.26696665_26696683delinsGCCGGCAGCGGCGGCGGGC GRCh38
NC_000001.10:g.27023156_27023174delinsGCCGGCAGCGGCGGCGGGC , CM000663.1:g.27023156_27023174delinsGCCGGCAGCGGCGGCGGGC GRCh37
NC_000001.9:g.26895743_26895761delinsGCCGGCAGCGGCGGCGGGC NCBI36
NG_029965.1:g.5635_5653delinsGCCGGCAGCGGCGGCGGGC , LRG_875:g.5635_5653delinsGCCGGCAGCGGCGGCGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.262_280delinsGCCGGCAGCGGCGGCGGGC MANE Select ENSP00000320485.7:p.Ala88=
ENST00000430799.7:c.-13+3048_-13+3066delinsGCCGGCAGCGGCGGCGGGC ENSP00000390317.3:n.-13+3048_-13+3066delinsGCCGGCAGCGGCGGCGGG...
ENST00000637465.1:c.-13+565_-13+583delinsGCCGGCAGCGGCGGCGGGC ENSP00000490650.1:n.-13+565_-13+583delinsGCCGGCAGCGGCGGCGGGC
ENST00000324856.11:c.262_280delinsGCCGGCAGCGGCGGCGGGC ENSP00000320485.7:p.Ala88=
ENST00000457599.6:c.262_280delinsGCCGGCAGCGGCGGCGGGC ENSP00000387636.2:p.Ala88=
NM_006015.4:c.262_280delinsGCCGGCAGCGGCGGCGGGC , LRG_875t1:c.262_280delinsGCCGGCAGCGGCGGCGGGC NP_006006.3:p.Ala88=
NM_139135.2:c.262_280delinsGCCGGCAGCGGCGGCGGGC NP_624361.1:p.Ala88=
NM_006015.5:c.262_280delinsGCCGGCAGCGGCGGCGGGC NP_006006.3:p.Ala88=
NM_139135.3:c.262_280delinsGCCGGCAGCGGCGGCGGGC NP_624361.1:p.Ala88=
NM_006015.6:c.262_280delinsGCCGGCAGCGGCGGCGGGC MANE Select NP_006006.3:p.Ala88=
NM_139135.4:c.262_280delinsGCCGGCAGCGGCGGCGGGC NP_624361.1:p.Ala88=