Canonical Allele Identifier: CA821296225
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778301_156778315del , CM000668.2:g.156778301_156778315del GRCh38
NC_000006.11:g.157099435_157099449del , CM000668.1:g.157099435_157099449del GRCh37
NC_000006.10:g.157141127_157141141del NCBI36
NG_032093.1:g.5372_5386del
NG_032093.2:g.5372_5386del
NG_066624.1:g.7276_7290del

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.621_635del MANE Select NP_001361757.1:p.Gln208_Gln212del
ENST00000636930.2:c.621_635del MANE Select ENSP00000490491.2:p.Gln208_Gln212del
NM_001346813.1:c.372_386del NP_001333742.1:p.Gln125_Gln129del
NM_001371656.1:c.621_635del NP_001358585.1:p.Gln208_Gln212del
NM_001374820.1:c.621_635del NP_001361749.1:p.Gln208_Gln212del
NM_017519.2:c.372_386del NP_059989.2:p.Gln125_Gln129del
NM_017519.3:c.621_635del NP_059989.3:p.Gln208_Gln212del
NM_020732.3:c.372_386del NP_065783.3:p.Gln125_Gln129del
NR_163974.1:n.212_226del
ENST00000346085.10:c.621_635del ENSP00000344546.5:p.Gln208_Gln212del
ENST00000346085.9:c.372_386del ENSP00000344546.4:p.Gln125_Gln129del
ENST00000350026.10:c.372_386del ENSP00000055163.7:p.Gln125_Gln129del
ENST00000350026.11:c.621_635del ENSP00000055163.8:p.Gln208_Gln212del
ENST00000350026.9:c.372_386del ENSP00000055163.7:p.Gln125_Gln129del
ENST00000414678.8:c.621_635del ENSP00000412835.3:p.Gln208_Gln212del
ENST00000637015.2:c.621_635del ENSP00000489729.2:p.Gln208_Gln212del
ENST00000647938.1:c.372_386del ENSP00000498155.1:p.Gln125_Gln129del
ENST00000674298.1:c.361_375del
XM_005267069.3:c.372_386del XP_005267126.2:p.Gln125_Gln129del
XM_011535984.2:c.372_386del XP_011534286.2:p.Gln125_Gln129del
XM_017011103.2:c.372_386del XP_016866592.1:p.Gln125_Gln129del
XM_017011104.1:c.372_386del XP_016866593.1:p.Gln125_Gln129del
XM_017011105.2:c.372_386del XP_016866594.1:p.Gln125_Gln129del
XM_017011106.2:c.372_386del XP_016866595.1:p.Gln125_Gln129del
XM_017011107.2:c.372_386del XP_016866596.1:p.Gln125_Gln129del
XR_002956289.1:n.455_469del
XR_943148.1:n.116_130del