Canonical Allele Identifier: CA204614
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200765_157200766del , CM000668.2:g.157200765_157200766del GRCh38
NC_000006.11:g.157521899_157521900del , CM000668.1:g.157521899_157521900del GRCh37
NC_000006.10:g.157563591_157563592del NCBI36
NG_032093.1:g.427836_427837del
NG_032093.2:g.427836_427837del
NG_066624.1:g.429740_429741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4381_4382del ENSP00000055163.8:p.Met1461ValfsTer?
ENST00000414678.8:c.4450_4451del ENSP00000412835.3:p.Met1484ValfsTer?
ENST00000637015.2:c.4669_4670del ENSP00000489729.2:p.Met1557ValfsTer?
ENST00000346085.10:c.4420_4421del ENSP00000344546.5:p.Met1474ValfsTer?
ENST00000350026.10:c.4132_4133del ENSP00000055163.7:p.Met1378ValfsTer?
ENST00000414678.7:c.2698_2699del ENSP00000412835.2:p.Met900ValfsTer?
ENST00000635849.1:c.1861_1862del ENSP00000490948.1:p.Met621ValfsTer?
ENST00000635957.1:c.1492_1493del ENSP00000490385.1:p.Met498ValfsTer?
ENST00000636227.1:n.3003_3004del
ENST00000636254.1:n.460_461del
ENST00000636930.2:c.4540_4541del MANE Select ENSP00000490491.2:p.Met1514ValfsTer?
ENST00000636940.1:n.2537_2538del
ENST00000637015.1:c.1908_1909del
ENST00000637568.1:c.1822_1823del
ENST00000637741.1:n.1206_1207del
ENST00000637810.1:c.1882_1883del ENSP00000489636.1:p.Met628ValfsTer?
ENST00000637904.1:c.2041_2042del ENSP00000490550.1:p.Met681ValfsTer?
ENST00000647938.1:c.4171_4172del ENSP00000498155.1:p.Met1391ValfsTer?
ENST00000346085.9:c.4171_4172del ENSP00000344546.4:p.Met1391ValfsTer?
ENST00000350026.9:c.4132_4133del ENSP00000055163.7:p.Met1378ValfsTer?
ENST00000414678.6:c.2698_2699del ENSP00000412835.2:p.Met900ValfsTer?
NM_017519.2:c.4132_4133del NP_059989.2:p.Met1378ValfsTer?
NM_020732.3:c.4171_4172del NP_065783.3:p.Met1391ValfsTer?
XM_005267069.3:c.4291_4292del XP_005267126.2:p.Met1431ValfsTer?
XM_011535984.1:c.3370_3371del XP_011534286.1:p.Met1124ValfsTer?
XM_011535985.1:c.3190_3191del XP_011534287.1:p.Met1064ValfsTer?
XM_011535986.1:c.2950_2951del XP_011534288.1:p.Met984ValfsTer?
XM_011535987.1:c.2569_2570del XP_011534289.1:p.Met857ValfsTer?
XM_011535988.1:c.1432_1433del XP_011534290.1:p.Met478ValfsTer?
NM_001346813.1:c.4291_4292del NP_001333742.1:p.Met1431ValfsTer?
NM_001363725.1:c.2041_2042del NP_001350654.1:p.Met681ValfsTer?
XM_011535984.2:c.4501_4502del XP_011534286.2:p.Met1501ValfsTer?
XM_011535988.3:c.1432_1433del XP_011534290.1:p.Met478ValfsTer?
XM_017011103.2:c.4402_4403del XP_016866592.1:p.Met1468ValfsTer?
XM_017011104.1:c.4372_4373del XP_016866593.1:p.Met1458ValfsTer?
XM_017011105.2:c.4342_4343del XP_016866594.1:p.Met1448ValfsTer?
XM_017011106.2:c.4213_4214del XP_016866595.1:p.Met1405ValfsTer?
XM_017011107.2:c.4192_4193del XP_016866596.1:p.Met1398ValfsTer?
XR_002956289.1:n.4487_4488del
NM_001363725.2:c.2041_2042del NP_001350654.1:p.Met681ValfsTer?
NM_001371656.1:c.4420_4421del NP_001358585.1:p.Met1474ValfsTer?
NM_001374820.1:c.4420_4421del NP_001361749.1:p.Met1474ValfsTer?
NM_001374828.1:c.4540_4541del MANE Select NP_001361757.1:p.Met1514ValfsTer?
NM_017519.3:c.4381_4382del NP_059989.3:p.Met1461ValfsTer?