Canonical Allele Identifier: CA10575556
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207604_157207614del , CM000668.2:g.157207604_157207614del GRCh38
NC_000006.11:g.157528738_157528748del , CM000668.1:g.157528738_157528748del GRCh37
NC_000006.10:g.157570430_157570440del NCBI36
NG_032093.1:g.434675_434685del
NG_032093.2:g.434675_434685del
NG_066624.1:g.436579_436589del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.6673_6683del ENSP00000055163.8:p.Ser2225LeufsTer?
ENST00000414678.8:c.6742_6752del ENSP00000412835.3:p.Ser2248LeufsTer?
ENST00000637015.2:c.6961_6971del ENSP00000489729.2:p.Ser2321LeufsTer?
ENST00000346085.10:c.6712_6722del ENSP00000344546.5:p.Ser2238LeufsTer?
ENST00000350026.10:c.6424_6434del ENSP00000055163.7:p.Ser2142LeufsTer?
ENST00000414678.7:c.4990_5000del ENSP00000412835.2:p.Ser1664LeufsTer?
ENST00000635849.1:c.4153_4163del ENSP00000490948.1:p.Ser1385LeufsTer?
ENST00000635928.1:c.875+113_875+123del ENSP00000489717.1:n.875+113_875+123del
ENST00000635957.1:c.3784_3794del ENSP00000490385.1:p.Ser1262LeufsTer?
ENST00000636227.1:n.5295_5305del
ENST00000636254.1:n.2752_2762del
ENST00000636930.2:c.6832_6842del MANE Select ENSP00000490491.2:p.Ser2278LeufsTer?
ENST00000636940.1:n.4829_4839del
ENST00000637015.1:c.4200_4210del
ENST00000637568.1:c.4114_4124del
ENST00000637741.1:n.3498_3508del
ENST00000637810.1:c.4174_4184del ENSP00000489636.1:p.Ser1392LeufsTer?
ENST00000637904.1:c.4333_4343del ENSP00000490550.1:p.Ser1445LeufsTer?
ENST00000637933.1:n.3947_3957del
ENST00000647938.1:c.6463_6473del ENSP00000498155.1:p.Ser2155LeufsTer?
ENST00000346085.9:c.6463_6473del ENSP00000344546.4:p.Ser2155LeufsTer?
ENST00000350026.9:c.6424_6434del ENSP00000055163.7:p.Ser2142LeufsTer?
ENST00000414678.6:c.4990_5000del ENSP00000412835.2:p.Ser1664LeufsTer?
NM_017519.2:c.6424_6434del NP_059989.2:p.Ser2142LeufsTer?
NM_020732.3:c.6463_6473del NP_065783.3:p.Ser2155LeufsTer?
XM_005267069.3:c.6583_6593del XP_005267126.2:p.Ser2195LeufsTer?
XM_011535984.1:c.5662_5672del XP_011534286.1:p.Ser1888LeufsTer?
XM_011535985.1:c.5482_5492del XP_011534287.1:p.Ser1828LeufsTer?
XM_011535986.1:c.5242_5252del XP_011534288.1:p.Ser1748LeufsTer?
XM_011535987.1:c.4861_4871del XP_011534289.1:p.Ser1621LeufsTer?
XM_011535988.1:c.3724_3734del XP_011534290.1:p.Ser1242LeufsTer?
NM_001346813.1:c.6583_6593del NP_001333742.1:p.Ser2195LeufsTer?
NM_001363725.1:c.4333_4343del NP_001350654.1:p.Ser1445LeufsTer?
XM_011535984.2:c.6793_6803del XP_011534286.2:p.Ser2265LeufsTer?
XM_011535988.3:c.3724_3734del XP_011534290.1:p.Ser1242LeufsTer?
XM_017011103.2:c.6694_6704del XP_016866592.1:p.Ser2232LeufsTer?
XM_017011104.1:c.6664_6674del XP_016866593.1:p.Ser2222LeufsTer?
XM_017011105.2:c.6634_6644del XP_016866594.1:p.Ser2212LeufsTer?
XM_017011106.2:c.6505_6515del XP_016866595.1:p.Ser2169LeufsTer?
XM_017011107.2:c.6484_6494del XP_016866596.1:p.Ser2162LeufsTer?
XR_002956289.1:n.6779_6789del
NM_001363725.2:c.4333_4343del NP_001350654.1:p.Ser1445LeufsTer?
NM_001371656.1:c.6712_6722del NP_001358585.1:p.Ser2238LeufsTer?
NM_001374820.1:c.6712_6722del NP_001361749.1:p.Ser2238LeufsTer?
NM_001374828.1:c.6832_6842del MANE Select NP_001361757.1:p.Ser2278LeufsTer?
NM_017519.3:c.6673_6683del NP_059989.3:p.Ser2225LeufsTer?