Canonical Allele Identifier: CA2573151656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354613
ClinVar RCV Id: RCV001866512
dbSNP Id: rs2151536071

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2773del ENSP00000455997.2:n.*2773del
ENST00000642206.2:c.4271del ENSP00000495146.2:p.Val1424GlufsTer6
ENST00000642365.2:c.4421del ENSP00000495459.2:p.Val1474GlufsTer6
ENST00000644417.2:c.*4804del ENSP00000493912.2:n.*4804del
ENST00000646464.2:c.*7173del ENSP00000496610.2:n.*7173del
ENST00000219476.9:c.4424del MANE Select ENSP00000219476.3:p.Val1475GlufsTer6
ENST00000350773.9:c.4355del ENSP00000344383.4:p.Val1452GlufsTer6
ENST00000401874.7:c.4223del ENSP00000384468.2:p.Val1408GlufsTer6
ENST00000568454.6:c.4256del ENSP00000454487.1:p.Val1419GlufsTer6
ENST00000569110.2:c.660del
ENST00000569930.2:n.2306del
ENST00000642365.1:c.3078del
ENST00000642561.1:c.4295del ENSP00000495099.1:p.Val1432GlufsTer6
ENST00000642728.1:n.606del
ENST00000642797.1:c.4226del ENSP00000493846.1:p.Val1409GlufsTer6
ENST00000642936.1:c.4292del ENSP00000494514.1:p.Val1431GlufsTer6
ENST00000643088.1:c.4223del ENSP00000494747.1:p.Val1408GlufsTer6
ENST00000643177.1:n.438del
ENST00000643426.1:n.2072del
ENST00000643946.1:c.4355del ENSP00000495927.1:p.Val1452GlufsTer6
ENST00000644043.1:c.4295del ENSP00000496262.1:p.Val1432GlufsTer6
ENST00000644329.1:c.4223del ENSP00000496611.1:p.Val1408GlufsTer6
ENST00000644335.1:c.4226del ENSP00000496317.1:p.Val1409GlufsTer6
ENST00000644399.1:c.4345del
ENST00000645024.1:n.2508del
ENST00000646388.1:c.4424del ENSP00000495921.1:p.Val1475GlufsTer6
ENST00000646634.1:n.3239del
ENST00000646674.1:n.1676del
ENST00000647042.1:n.1647del
ENST00000647180.1:n.1537del
ENST00000219476.7:c.4424del ENSP00000219476.3:p.Val1475GlufsTer6
ENST00000350773.8:c.4355del ENSP00000344383.4:p.Val1452GlufsTer6
ENST00000382538.10:c.4079del ENSP00000371978.6:p.Val1360GlufsTer6
ENST00000401874.6:c.4223del ENSP00000384468.2:p.Val1408GlufsTer6
ENST00000439117.6:c.*3591del ENSP00000406980.2:n.*3591del
ENST00000439673.6:c.4115del ENSP00000399232.2:p.Val1372GlufsTer6
ENST00000497886.5:n.2182del
ENST00000568454.5:c.4256del ENSP00000454487.1:p.Val1419GlufsTer6
ENST00000569110.1:c.606del
ENST00000569930.1:n.1539del
NM_000548.3:c.4424del , LRG_487t1:c.4424del NP_000539.2:p.Val1475GlufsTer6
NM_001077183.1:c.4223del NP_001070651.1:p.Val1408GlufsTer6
NM_001114382.1:c.4355del NP_001107854.1:p.Val1452GlufsTer6
XM_005255529.3:c.4295del XP_005255586.2:p.Val1432GlufsTer6
XM_005255531.3:c.4226del XP_005255588.2:p.Val1409GlufsTer6
XM_011522636.1:c.4478del XP_011520938.1:p.Val1493GlufsTer6
XM_011522637.1:c.4475del XP_011520939.1:p.Val1492GlufsTer6
XM_011522638.1:c.4367del XP_011520940.1:p.Val1456GlufsTer6
XM_011522639.1:c.4349del XP_011520941.1:p.Val1450GlufsTer6
XM_011522640.1:c.4346del XP_011520942.1:p.Val1449GlufsTer6
XM_011522641.1:c.4115del XP_011520943.1:p.Val1372GlufsTer6
NM_000548.4:c.4424del NP_000539.2:p.Val1475GlufsTer6
NM_001077183.2:c.4223del NP_001070651.1:p.Val1408GlufsTer6
NM_001114382.2:c.4355del NP_001107854.1:p.Val1452GlufsTer6
NM_001318827.1:c.4115del NP_001305756.1:p.Val1372GlufsTer6
NM_001318829.1:c.4079del NP_001305758.1:p.Val1360GlufsTer6
NM_001318831.1:c.3692del NP_001305760.1:p.Val1231GlufsTer6
NM_001318832.1:c.4256del NP_001305761.1:p.Val1419GlufsTer6
NM_001363528.1:c.4226del NP_001350457.1:p.Val1409GlufsTer6
NM_021055.2:c.4295del NP_066399.2:p.Val1432GlufsTer6
XM_005255531.4:c.4226del XP_005255588.2:p.Val1409GlufsTer6
XM_011522636.2:c.4478del XP_011520938.1:p.Val1493GlufsTer6
XM_011522637.2:c.4475del XP_011520939.1:p.Val1492GlufsTer6
XM_011522638.2:c.4640del XP_011520940.2:p.Val1547GlufsTer6
XM_011522639.2:c.4349del XP_011520941.1:p.Val1450GlufsTer6
XM_011522640.2:c.4346del XP_011520942.1:p.Val1449GlufsTer6
XM_017023615.1:c.4421del XP_016879104.1:p.Val1474GlufsTer6
XM_017023616.1:c.4292del XP_016879105.1:p.Val1431GlufsTer6
XM_017023617.1:c.4388del XP_016879106.1:p.Val1463GlufsTer6
XM_017023618.1:c.3134del XP_016879107.1:p.Val1045GlufsTer6
XM_024450413.1:c.4223del XP_024306181.1:p.Val1408GlufsTer6
NM_000548.5:c.4424del MANE Select NP_000539.2:p.Val1475GlufsTer6
NM_001370404.1:c.4292del NP_001357333.1:p.Val1431GlufsTer6
NM_001370405.1:c.4295del NP_001357334.1:p.Val1432GlufsTer6
NM_001077183.3:c.4223del NP_001070651.1:p.Val1408GlufsTer6
NM_001114382.3:c.4355del NP_001107854.1:p.Val1452GlufsTer6
NM_001318827.2:c.4115del NP_001305756.1:p.Val1372GlufsTer6
NM_001318829.2:c.4079del NP_001305758.1:p.Val1360GlufsTer6
NM_001318831.2:c.3692del NP_001305760.1:p.Val1231GlufsTer6
NM_001318832.2:c.4256del NP_001305761.1:p.Val1419GlufsTer6
NM_001363528.2:c.4226del NP_001350457.1:p.Val1409GlufsTer6
NM_021055.3:c.4295del NP_066399.2:p.Val1432GlufsTer6