Canonical Allele Identifier: CA16043615
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207498del , CM000668.2:g.157207498del GRCh38
NC_000006.11:g.157528632del , CM000668.1:g.157528632del GRCh37
NC_000006.10:g.157570324del NCBI36
NG_032093.1:g.434569del
NG_032093.2:g.434569del
NG_066624.1:g.436473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.6567del ENSP00000055163.8:p.Asp2191IlefsTer24
ENST00000414678.8:c.6636del ENSP00000412835.3:p.Asp2214IlefsTer24
ENST00000637015.2:c.6855del ENSP00000489729.2:p.Asp2287IlefsTer24
ENST00000346085.10:c.6606del ENSP00000344546.5:p.Asp2204IlefsTer24
ENST00000350026.10:c.6318del ENSP00000055163.7:p.Asp2108IlefsTer24
ENST00000414678.7:c.4884del ENSP00000412835.2:p.Asp1630IlefsTer24
ENST00000635849.1:c.4047del ENSP00000490948.1:p.Asp1351IlefsTer24
ENST00000635928.1:c.875+7del ENSP00000489717.1:n.875+7del
ENST00000635957.1:c.3678del ENSP00000490385.1:p.Asp1228IlefsTer24
ENST00000636227.1:n.5189del
ENST00000636254.1:n.2646del
ENST00000636930.2:c.6726del MANE Select ENSP00000490491.2:p.Asp2244IlefsTer24
ENST00000636940.1:n.4723del
ENST00000637015.1:c.4094del
ENST00000637568.1:c.4008del
ENST00000637741.1:n.3392del
ENST00000637810.1:c.4068del ENSP00000489636.1:p.Asp1358IlefsTer24
ENST00000637904.1:c.4227del ENSP00000490550.1:p.Asp1411IlefsTer24
ENST00000637933.1:n.3841del
ENST00000647938.1:c.6357del ENSP00000498155.1:p.Asp2121IlefsTer24
ENST00000346085.9:c.6357del ENSP00000344546.4:p.Asp2121IlefsTer24
ENST00000350026.9:c.6318del ENSP00000055163.7:p.Asp2108IlefsTer24
ENST00000414678.6:c.4884del ENSP00000412835.2:p.Asp1630IlefsTer24
NM_017519.2:c.6318del NP_059989.2:p.Asp2108IlefsTer24
NM_020732.3:c.6357del NP_065783.3:p.Asp2121IlefsTer24
XM_005267069.3:c.6477del XP_005267126.2:p.Asp2161IlefsTer24
XM_011535984.1:c.5556del XP_011534286.1:p.Asp1854IlefsTer24
XM_011535985.1:c.5376del XP_011534287.1:p.Asp1794IlefsTer24
XM_011535986.1:c.5136del XP_011534288.1:p.Asp1714IlefsTer24
XM_011535987.1:c.4755del XP_011534289.1:p.Asp1587IlefsTer24
XM_011535988.1:c.3618del XP_011534290.1:p.Asp1208IlefsTer24
NM_001346813.1:c.6477del NP_001333742.1:p.Asp2161IlefsTer24
NM_001363725.1:c.4227del NP_001350654.1:p.Asp1411IlefsTer24
XM_011535984.2:c.6687del XP_011534286.2:p.Asp2231IlefsTer24
XM_011535988.3:c.3618del XP_011534290.1:p.Asp1208IlefsTer24
XM_017011103.2:c.6588del XP_016866592.1:p.Asp2198IlefsTer24
XM_017011104.1:c.6558del XP_016866593.1:p.Asp2188IlefsTer24
XM_017011105.2:c.6528del XP_016866594.1:p.Asp2178IlefsTer24
XM_017011106.2:c.6399del XP_016866595.1:p.Asp2135IlefsTer24
XM_017011107.2:c.6378del XP_016866596.1:p.Asp2128IlefsTer24
XR_002956289.1:n.6673del
NM_001363725.2:c.4227del NP_001350654.1:p.Asp1411IlefsTer24
NM_001371656.1:c.6606del NP_001358585.1:p.Asp2204IlefsTer24
NM_001374820.1:c.6606del NP_001361749.1:p.Asp2204IlefsTer24
NM_001374828.1:c.6726del MANE Select NP_001361757.1:p.Asp2244IlefsTer24
NM_017519.3:c.6567del NP_059989.3:p.Asp2191IlefsTer24