Canonical Allele Identifier: CA020774
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs397515137

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085281_2085289del , CM000678.2:g.2085281_2085289del GRCh38
NC_000016.9:g.2135282_2135290del , CM000678.1:g.2135282_2135290del GRCh37
NC_000016.8:g.2075283_2075291del NCBI36
NG_005895.1:g.40976_40984del , LRG_487:g.40976_40984del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2970_*2978del ENSP00000455997.2:n.*2970_*2978del
ENST00000642206.2:c.4468_4476del ENSP00000495146.2:p.Asp1490_His1492del
ENST00000642365.2:c.4618_4626del ENSP00000495459.2:p.Asp1540_His1542del
ENST00000644417.2:c.*5001_*5009del ENSP00000493912.2:n.*5001_*5009del
ENST00000646464.2:c.*7370_*7378del ENSP00000496610.2:n.*7370_*7378del
ENST00000219476.9:c.4621_4629del MANE Select ENSP00000219476.3:p.Asp1541_His1543del
ENST00000350773.9:c.4552_4560del ENSP00000344383.4:p.Asp1518_His1520del
ENST00000401874.7:c.4420_4428del ENSP00000384468.2:p.Asp1474_His1476del
ENST00000568454.6:c.4453_4461del ENSP00000454487.1:p.Asp1485_His1487del
ENST00000569110.2:c.844_852del
ENST00000569930.2:n.2503_2511del
ENST00000642365.1:c.3275_3283del
ENST00000642561.1:c.4492_4500del ENSP00000495099.1:p.Asp1498_His1500del
ENST00000642728.1:n.803_811del
ENST00000642791.1:n.218_226del
ENST00000642797.1:c.4423_4431del ENSP00000493846.1:p.Asp1475_His1477del
ENST00000642936.1:c.4489_4497del ENSP00000494514.1:p.Asp1497_His1499del
ENST00000643088.1:c.4414_4422del ENSP00000494747.1:p.Asp1472_His1474del
ENST00000643177.1:n.635_643del
ENST00000643426.1:n.2269_2277del
ENST00000643946.1:c.4546_4554del ENSP00000495927.1:p.Asp1516_His1518del
ENST00000644043.1:c.4492_4500del ENSP00000496262.1:p.Asp1498_His1500del
ENST00000644278.1:n.103_111del
ENST00000644329.1:c.4420_4428del ENSP00000496611.1:p.Asp1474_His1476del
ENST00000644335.1:c.4417_4425del ENSP00000496317.1:p.Asp1473_His1475del
ENST00000644399.1:c.4542_4550del
ENST00000645024.1:n.2705_2713del
ENST00000646388.1:c.4615_4623del ENSP00000495921.1:p.Asp1539_His1541del
ENST00000646634.1:n.3436_3444del
ENST00000646674.1:n.1873_1881del
ENST00000647042.1:n.1844_1852del
ENST00000647180.1:n.1734_1742del
ENST00000219476.7:c.4621_4629del ENSP00000219476.3:p.Asp1541_His1543del
ENST00000350773.8:c.4552_4560del ENSP00000344383.4:p.Asp1518_His1520del
ENST00000382538.10:c.4276_4284del ENSP00000371978.6:p.Asp1426_His1428del
ENST00000401874.6:c.4420_4428del ENSP00000384468.2:p.Asp1474_His1476del
ENST00000439117.6:c.*3788_*3796del ENSP00000406980.2:n.*3788_*3796del
ENST00000439673.6:c.4312_4320del ENSP00000399232.2:p.Asp1438_His1440del
ENST00000497886.5:n.2379_2387del
ENST00000568454.5:c.4453_4461del ENSP00000454487.1:p.Asp1485_His1487del
ENST00000569110.1:c.803_811del
ENST00000569930.1:n.1736_1744del
NM_000548.3:c.4621_4629del , LRG_487t1:c.4621_4629del NP_000539.2:p.Asp1541_His1543del
NM_001077183.1:c.4420_4428del NP_001070651.1:p.Asp1474_His1476del
NM_001114382.1:c.4552_4560del NP_001107854.1:p.Asp1518_His1520del
XM_005255529.3:c.4492_4500del XP_005255586.2:p.Asp1498_His1500del
XM_005255531.3:c.4423_4431del XP_005255588.2:p.Asp1475_His1477del
XM_011522636.1:c.4675_4683del XP_011520938.1:p.Asp1559_His1561del
XM_011522637.1:c.4672_4680del XP_011520939.1:p.Asp1558_His1560del
XM_011522638.1:c.4564_4572del XP_011520940.1:p.Asp1522_His1524del
XM_011522639.1:c.4546_4554del XP_011520941.1:p.Asp1516_His1518del
XM_011522640.1:c.4543_4551del XP_011520942.1:p.Asp1515_His1517del
XM_011522641.1:c.4312_4320del XP_011520943.1:p.Asp1438_His1440del
NM_000548.4:c.4621_4629del NP_000539.2:p.Asp1541_His1543del
NM_001077183.2:c.4420_4428del NP_001070651.1:p.Asp1474_His1476del
NM_001114382.2:c.4552_4560del NP_001107854.1:p.Asp1518_His1520del
NM_001318827.1:c.4312_4320del NP_001305756.1:p.Asp1438_His1440del
NM_001318829.1:c.4276_4284del NP_001305758.1:p.Asp1426_His1428del
NM_001318831.1:c.3889_3897del NP_001305760.1:p.Asp1297_His1299del
NM_001318832.1:c.4453_4461del NP_001305761.1:p.Asp1485_His1487del
NM_001363528.1:c.4423_4431del NP_001350457.1:p.Asp1475_His1477del
NM_021055.2:c.4492_4500del NP_066399.2:p.Asp1498_His1500del
XM_005255531.4:c.4423_4431del XP_005255588.2:p.Asp1475_His1477del
XM_011522636.2:c.4675_4683del XP_011520938.1:p.Asp1559_His1561del
XM_011522637.2:c.4672_4680del XP_011520939.1:p.Asp1558_His1560del
XM_011522638.2:c.4837_4845del XP_011520940.2:p.Asp1613_His1615del
XM_011522639.2:c.4546_4554del XP_011520941.1:p.Asp1516_His1518del
XM_011522640.2:c.4543_4551del XP_011520942.1:p.Asp1515_His1517del
XM_017023615.1:c.4618_4626del XP_016879104.1:p.Asp1540_His1542del
XM_017023616.1:c.4489_4497del XP_016879105.1:p.Asp1497_His1499del
XM_017023617.1:c.4585_4593del XP_016879106.1:p.Asp1529_His1531del
XM_017023618.1:c.3331_3339del XP_016879107.1:p.Asp1111_His1113del
XM_024450413.1:c.4420_4428del XP_024306181.1:p.Asp1474_His1476del
NM_000548.5:c.4621_4629del MANE Select NP_000539.2:p.Asp1541_His1543del
NM_001370404.1:c.4489_4497del NP_001357333.1:p.Asp1497_His1499del
NM_001370405.1:c.4492_4500del NP_001357334.1:p.Asp1498_His1500del
NM_001077183.3:c.4420_4428del NP_001070651.1:p.Asp1474_His1476del
NM_001114382.3:c.4552_4560del NP_001107854.1:p.Asp1518_His1520del
NM_001318827.2:c.4312_4320del NP_001305756.1:p.Asp1438_His1440del
NM_001318829.2:c.4276_4284del NP_001305758.1:p.Asp1426_His1428del
NM_001318831.2:c.3889_3897del NP_001305760.1:p.Asp1297_His1299del
NM_001318832.2:c.4453_4461del NP_001305761.1:p.Asp1485_His1487del
NM_001363528.2:c.4423_4431del NP_001350457.1:p.Asp1475_His1477del
NM_021055.3:c.4492_4500del NP_066399.2:p.Asp1498_His1500del