Canonical Allele Identifier: CA2580090982
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995874
ClinVar RCV Id: RCV002801625

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084646_2084648del , CM000678.2:g.2084646_2084648del GRCh38
NC_000016.9:g.2134647_2134649del , CM000678.1:g.2134647_2134649del GRCh37
NC_000016.8:g.2074648_2074650del NCBI36
NG_005895.1:g.40341_40343del , LRG_487:g.40341_40343del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2773_*2775del ENSP00000455997.2:n.*2773_*2775del
ENST00000642206.2:c.4271_4273del ENSP00000495146.2:p.Val1424del
ENST00000642365.2:c.4421_4423del ENSP00000495459.2:p.Val1474del
ENST00000644417.2:c.*4804_*4806del ENSP00000493912.2:n.*4804_*4806del
ENST00000646464.2:c.*7173_*7175del ENSP00000496610.2:n.*7173_*7175del
ENST00000219476.9:c.4424_4426del MANE Select ENSP00000219476.3:p.Val1475del
ENST00000350773.9:c.4355_4357del ENSP00000344383.4:p.Val1452del
ENST00000401874.7:c.4223_4225del ENSP00000384468.2:p.Val1408del
ENST00000568454.6:c.4256_4258del ENSP00000454487.1:p.Val1419del
ENST00000569110.2:c.660_662del
ENST00000569930.2:n.2306_2308del
ENST00000642365.1:c.3078_3080del
ENST00000642561.1:c.4295_4297del ENSP00000495099.1:p.Val1432del
ENST00000642728.1:n.606_608del
ENST00000642797.1:c.4226_4228del ENSP00000493846.1:p.Val1409del
ENST00000642936.1:c.4292_4294del ENSP00000494514.1:p.Val1431del
ENST00000643088.1:c.4223_4225del ENSP00000494747.1:p.Val1408del
ENST00000643177.1:n.438_440del
ENST00000643426.1:n.2072_2074del
ENST00000643946.1:c.4355_4357del ENSP00000495927.1:p.Val1452del
ENST00000644043.1:c.4295_4297del ENSP00000496262.1:p.Val1432del
ENST00000644329.1:c.4223_4225del ENSP00000496611.1:p.Val1408del
ENST00000644335.1:c.4226_4228del ENSP00000496317.1:p.Val1409del
ENST00000644399.1:c.4345_4347del
ENST00000645024.1:n.2508_2510del
ENST00000646388.1:c.4424_4426del ENSP00000495921.1:p.Val1475del
ENST00000646634.1:n.3239_3241del
ENST00000646674.1:n.1676_1678del
ENST00000647042.1:n.1647_1649del
ENST00000647180.1:n.1537_1539del
ENST00000219476.7:c.4424_4426del ENSP00000219476.3:p.Val1475del
ENST00000350773.8:c.4355_4357del ENSP00000344383.4:p.Val1452del
ENST00000382538.10:c.4079_4081del ENSP00000371978.6:p.Val1360del
ENST00000401874.6:c.4223_4225del ENSP00000384468.2:p.Val1408del
ENST00000439117.6:c.*3591_*3593del ENSP00000406980.2:n.*3591_*3593del
ENST00000439673.6:c.4115_4117del ENSP00000399232.2:p.Val1372del
ENST00000497886.5:n.2182_2184del
ENST00000568454.5:c.4256_4258del ENSP00000454487.1:p.Val1419del
ENST00000569110.1:c.606_608del
ENST00000569930.1:n.1539_1541del
NM_000548.3:c.4424_4426del , LRG_487t1:c.4424_4426del NP_000539.2:p.Val1475del
NM_001077183.1:c.4223_4225del NP_001070651.1:p.Val1408del
NM_001114382.1:c.4355_4357del NP_001107854.1:p.Val1452del
XM_005255529.3:c.4295_4297del XP_005255586.2:p.Val1432del
XM_005255531.3:c.4226_4228del XP_005255588.2:p.Val1409del
XM_011522636.1:c.4478_4480del XP_011520938.1:p.Val1493del
XM_011522637.1:c.4475_4477del XP_011520939.1:p.Val1492del
XM_011522638.1:c.4367_4369del XP_011520940.1:p.Val1456del
XM_011522639.1:c.4349_4351del XP_011520941.1:p.Val1450del
XM_011522640.1:c.4346_4348del XP_011520942.1:p.Val1449del
XM_011522641.1:c.4115_4117del XP_011520943.1:p.Val1372del
NM_000548.4:c.4424_4426del NP_000539.2:p.Val1475del
NM_001077183.2:c.4223_4225del NP_001070651.1:p.Val1408del
NM_001114382.2:c.4355_4357del NP_001107854.1:p.Val1452del
NM_001318827.1:c.4115_4117del NP_001305756.1:p.Val1372del
NM_001318829.1:c.4079_4081del NP_001305758.1:p.Val1360del
NM_001318831.1:c.3692_3694del NP_001305760.1:p.Val1231del
NM_001318832.1:c.4256_4258del NP_001305761.1:p.Val1419del
NM_001363528.1:c.4226_4228del NP_001350457.1:p.Val1409del
NM_021055.2:c.4295_4297del NP_066399.2:p.Val1432del
XM_005255531.4:c.4226_4228del XP_005255588.2:p.Val1409del
XM_011522636.2:c.4478_4480del XP_011520938.1:p.Val1493del
XM_011522637.2:c.4475_4477del XP_011520939.1:p.Val1492del
XM_011522638.2:c.4640_4642del XP_011520940.2:p.Val1547del
XM_011522639.2:c.4349_4351del XP_011520941.1:p.Val1450del
XM_011522640.2:c.4346_4348del XP_011520942.1:p.Val1449del
XM_017023615.1:c.4421_4423del XP_016879104.1:p.Val1474del
XM_017023616.1:c.4292_4294del XP_016879105.1:p.Val1431del
XM_017023617.1:c.4388_4390del XP_016879106.1:p.Val1463del
XM_017023618.1:c.3134_3136del XP_016879107.1:p.Val1045del
XM_024450413.1:c.4223_4225del XP_024306181.1:p.Val1408del
NM_000548.5:c.4424_4426del MANE Select NP_000539.2:p.Val1475del
NM_001370404.1:c.4292_4294del NP_001357333.1:p.Val1431del
NM_001370405.1:c.4295_4297del NP_001357334.1:p.Val1432del
NM_001077183.3:c.4223_4225del NP_001070651.1:p.Val1408del
NM_001114382.3:c.4355_4357del NP_001107854.1:p.Val1452del
NM_001318827.2:c.4115_4117del NP_001305756.1:p.Val1372del
NM_001318829.2:c.4079_4081del NP_001305758.1:p.Val1360del
NM_001318831.2:c.3692_3694del NP_001305760.1:p.Val1231del
NM_001318832.2:c.4256_4258del NP_001305761.1:p.Val1419del
NM_001363528.2:c.4226_4228del NP_001350457.1:p.Val1409del
NM_021055.3:c.4295_4297del NP_066399.2:p.Val1432del