Canonical Allele Identifier: CA1160180711
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696664_26696679delinsAGCCGGCAGCGGCGGC , CM000663.2:g.26696664_26696679delinsAGCCGGCAGCGGCGGC GRCh38
NC_000001.10:g.27023155_27023170delinsAGCCGGCAGCGGCGGC , CM000663.1:g.27023155_27023170delinsAGCCGGCAGCGGCGGC GRCh37
NC_000001.9:g.26895742_26895757delinsAGCCGGCAGCGGCGGC NCBI36
NG_029965.1:g.5634_5649delinsAGCCGGCAGCGGCGGC , LRG_875:g.5634_5649delinsAGCCGGCAGCGGCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.261_276delinsAGCCGGCAGCGGCGGC MANE Select ENSP00000320485.7:p.Gly87=
ENST00000430799.7:c.-13+3047_-13+3062delinsAGCCGGCAGCGGCGGC ENSP00000390317.3:n.-13+3047_-13+3062delinsAGCCGGCAGCGGCGGC
ENST00000637465.1:c.-13+564_-13+579delinsAGCCGGCAGCGGCGGC ENSP00000490650.1:n.-13+564_-13+579delinsAGCCGGCAGCGGCGGC
ENST00000324856.11:c.261_276delinsAGCCGGCAGCGGCGGC ENSP00000320485.7:p.Gly87=
ENST00000457599.6:c.261_276delinsAGCCGGCAGCGGCGGC ENSP00000387636.2:p.Gly87=
NM_006015.4:c.261_276delinsAGCCGGCAGCGGCGGC , LRG_875t1:c.261_276delinsAGCCGGCAGCGGCGGC NP_006006.3:p.Gly87=
NM_139135.2:c.261_276delinsAGCCGGCAGCGGCGGC NP_624361.1:p.Gly87=
NM_006015.5:c.261_276delinsAGCCGGCAGCGGCGGC NP_006006.3:p.Gly87=
NM_139135.3:c.261_276delinsAGCCGGCAGCGGCGGC NP_624361.1:p.Gly87=
NM_006015.6:c.261_276delinsAGCCGGCAGCGGCGGC MANE Select NP_006006.3:p.Gly87=
NM_139135.4:c.261_276delinsAGCCGGCAGCGGCGGC NP_624361.1:p.Gly87=