Canonical Allele Identifier: CA015668
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49623
ClinVar RCV Id: RCV002399400
dbSNP Id: rs137854371

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2070499_2070500del , CM000678.2:g.2070499_2070500del GRCh38
NC_000016.9:g.2120500_2120501del , CM000678.1:g.2120500_2120501del GRCh37
NC_000016.8:g.2060501_2060502del NCBI36
NG_005895.1:g.26194_26195del , LRG_487:g.26194_26195del

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*307_*308del ENSP00000455997.2:n.*307_*308del
ENST00000642206.2:c.1805_1806del ENSP00000495146.2:p.Tyr602Ter
ENST00000642365.2:c.1760_1761del ENSP00000495459.2:p.Tyr587Ter
ENST00000644417.2:c.*1197_*1198del ENSP00000493912.2:n.*1197_*1198del
ENST00000646464.2:c.*1365_*1366del ENSP00000496610.2:n.*1365_*1366del
ENST00000219476.9:c.1760_1761del MANE Select ENSP00000219476.3:p.Tyr587Ter
ENST00000350773.9:c.1760_1761del ENSP00000344383.4:p.Tyr587Ter
ENST00000401874.7:c.1760_1761del ENSP00000384468.2:p.Tyr587Ter
ENST00000568454.6:c.1793_1794del ENSP00000454487.1:p.Tyr598Ter
ENST00000642365.1:c.417_418del
ENST00000642561.1:c.1760_1761del ENSP00000495099.1:p.Tyr587Ter
ENST00000642797.1:c.1760_1761del ENSP00000493846.1:p.Tyr587Ter
ENST00000642936.1:c.1760_1761del ENSP00000494514.1:p.Tyr587Ter
ENST00000643088.1:c.1760_1761del ENSP00000494747.1:p.Tyr587Ter
ENST00000643298.1:c.*1262_*1263del ENSP00000494393.1:n.*1262_*1263del
ENST00000643946.1:c.1760_1761del ENSP00000495927.1:p.Tyr587Ter
ENST00000644043.1:c.1760_1761del ENSP00000496262.1:p.Tyr587Ter
ENST00000644135.1:c.*260_*261del ENSP00000495644.1:n.*260_*261del
ENST00000644329.1:c.1760_1761del ENSP00000496611.1:p.Tyr587Ter
ENST00000644335.1:c.1760_1761del ENSP00000496317.1:p.Tyr587Ter
ENST00000644399.1:c.1753_1754del
ENST00000644847.1:n.752_753del
ENST00000645552.1:n.40_41del
ENST00000646388.1:c.1760_1761del ENSP00000495921.1:p.Tyr587Ter
ENST00000646634.1:n.773_774del
ENST00000219476.7:c.1760_1761del ENSP00000219476.3:p.Tyr587Ter
ENST00000350773.8:c.1760_1761del ENSP00000344383.4:p.Tyr587Ter
ENST00000382538.10:c.1613_1614del ENSP00000371978.6:p.Tyr538Ter
ENST00000401874.6:c.1760_1761del ENSP00000384468.2:p.Tyr587Ter
ENST00000439117.6:c.*1059_*1060del ENSP00000406980.2:n.*1059_*1060del
ENST00000439673.6:c.1649_1650del ENSP00000399232.2:p.Tyr550Ter
ENST00000488675.5:n.267_268del
ENST00000562474.1:n.485_486del
ENST00000568454.5:c.1793_1794del ENSP00000454487.1:p.Tyr598Ter
ENST00000568566.5:c.400_401del ENSP00000455997.1:n.400_401del
NM_000548.3:c.1760_1761del , LRG_487t1:c.1760_1761del NP_000539.2:p.Tyr587Ter
NM_001077183.1:c.1760_1761del NP_001070651.1:p.Tyr587Ter
NM_001114382.1:c.1760_1761del NP_001107854.1:p.Tyr587Ter
XM_005255529.3:c.1760_1761del XP_005255586.2:p.Tyr587Ter
XM_005255531.3:c.1760_1761del XP_005255588.2:p.Tyr587Ter
XM_011522636.1:c.1760_1761del XP_011520938.1:p.Tyr587Ter
XM_011522637.1:c.1760_1761del XP_011520939.1:p.Tyr587Ter
XM_011522638.1:c.1649_1650del XP_011520940.1:p.Tyr550Ter
XM_011522639.1:c.1760_1761del XP_011520941.1:p.Tyr587Ter
XM_011522640.1:c.1760_1761del XP_011520942.1:p.Tyr587Ter
XM_011522641.1:c.1649_1650del XP_011520943.1:p.Tyr550Ter
NM_000548.4:c.1760_1761del NP_000539.2:p.Tyr587Ter
NM_001077183.2:c.1760_1761del NP_001070651.1:p.Tyr587Ter
NM_001114382.2:c.1760_1761del NP_001107854.1:p.Tyr587Ter
NM_001318827.1:c.1649_1650del NP_001305756.1:p.Tyr550Ter
NM_001318829.1:c.1613_1614del NP_001305758.1:p.Tyr538Ter
NM_001318831.1:c.1160_1161del NP_001305760.1:p.Tyr387Ter
NM_001318832.1:c.1793_1794del NP_001305761.1:p.Tyr598Ter
NM_001363528.1:c.1760_1761del NP_001350457.1:p.Tyr587Ter
NM_021055.2:c.1760_1761del NP_066399.2:p.Tyr587Ter
XM_005255531.4:c.1760_1761del XP_005255588.2:p.Tyr587Ter
XM_011522636.2:c.1760_1761del XP_011520938.1:p.Tyr587Ter
XM_011522637.2:c.1760_1761del XP_011520939.1:p.Tyr587Ter
XM_011522638.2:c.1922_1923del XP_011520940.2:p.Tyr641Ter
XM_011522639.2:c.1760_1761del XP_011520941.1:p.Tyr587Ter
XM_011522640.2:c.1760_1761del XP_011520942.1:p.Tyr587Ter
XM_017023615.1:c.1760_1761del XP_016879104.1:p.Tyr587Ter
XM_017023616.1:c.1760_1761del XP_016879105.1:p.Tyr587Ter
XM_017023617.1:c.1922_1923del XP_016879106.1:p.Tyr641Ter
XM_017023618.1:c.416_417del XP_016879107.1:p.Tyr139Ter
XM_024450413.1:c.1760_1761del XP_024306181.1:p.Tyr587Ter
NM_000548.5:c.1760_1761del MANE Select NP_000539.2:p.Tyr587Ter
NM_001370404.1:c.1760_1761del NP_001357333.1:p.Tyr587Ter
NM_001370405.1:c.1760_1761del NP_001357334.1:p.Tyr587Ter
NM_001077183.3:c.1760_1761del NP_001070651.1:p.Tyr587Ter
NM_001114382.3:c.1760_1761del NP_001107854.1:p.Tyr587Ter
NM_001318827.2:c.1649_1650del NP_001305756.1:p.Tyr550Ter
NM_001318829.2:c.1613_1614del NP_001305758.1:p.Tyr538Ter
NM_001318831.2:c.1160_1161del NP_001305760.1:p.Tyr387Ter
NM_001318832.2:c.1793_1794del NP_001305761.1:p.Tyr598Ter
NM_001363528.2:c.1760_1761del NP_001350457.1:p.Tyr587Ter
NM_021055.3:c.1760_1761del NP_066399.2:p.Tyr587Ter