Canonical Allele Identifier: CA016589
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49190
ClinVar RCV Id: RCV000042446
dbSNP Id: rs137854234

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2071918_2071920del , CM000678.2:g.2071918_2071920del GRCh38
NC_000016.9:g.2121919_2121921del , CM000678.1:g.2121919_2121921del GRCh37
NC_000016.8:g.2061920_2061922del NCBI36
NG_005895.1:g.27613_27615del , LRG_487:g.27613_27615del

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*628_*630del ENSP00000455997.2:n.*628_*630del
ENST00000642206.2:c.2126_2128del ENSP00000495146.2:p.Leu709del
ENST00000642365.2:c.2081_2083del ENSP00000495459.2:p.Leu694del
ENST00000644417.2:c.*1518_*1520del ENSP00000493912.2:n.*1518_*1520del
ENST00000646464.2:c.*1686_*1688del ENSP00000496610.2:n.*1686_*1688del
ENST00000219476.9:c.2081_2083del MANE Select ENSP00000219476.3:p.Leu694del
ENST00000350773.9:c.2081_2083del ENSP00000344383.4:p.Leu694del
ENST00000401874.7:c.2081_2083del ENSP00000384468.2:p.Leu694del
ENST00000563346.2:n.259_261del
ENST00000568454.6:c.2114_2116del ENSP00000454487.1:p.Leu705del
ENST00000642365.1:c.738_740del
ENST00000642561.1:c.2081_2083del ENSP00000495099.1:p.Leu694del
ENST00000642797.1:c.2081_2083del ENSP00000493846.1:p.Leu694del
ENST00000642936.1:c.2081_2083del ENSP00000494514.1:p.Leu694del
ENST00000643088.1:c.2081_2083del ENSP00000494747.1:p.Leu694del
ENST00000643298.1:c.*1583_*1585del ENSP00000494393.1:n.*1583_*1585del
ENST00000643946.1:c.2081_2083del ENSP00000495927.1:p.Leu694del
ENST00000644043.1:c.2081_2083del ENSP00000496262.1:p.Leu694del
ENST00000644329.1:c.2081_2083del ENSP00000496611.1:p.Leu694del
ENST00000644335.1:c.2081_2083del ENSP00000496317.1:p.Leu694del
ENST00000644399.1:c.2074_2076del
ENST00000644847.1:n.1073_1075del
ENST00000645024.1:n.363_365del
ENST00000645552.1:n.361_363del
ENST00000646388.1:c.2081_2083del ENSP00000495921.1:p.Leu694del
ENST00000646464.1:c.134_136del ENSP00000496610.1:p.Leu45del
ENST00000646634.1:n.1094_1096del
ENST00000219476.7:c.2081_2083del ENSP00000219476.3:p.Leu694del
ENST00000350773.8:c.2081_2083del ENSP00000344383.4:p.Leu694del
ENST00000382538.10:c.1934_1936del ENSP00000371978.6:p.Leu645del
ENST00000401874.6:c.2081_2083del ENSP00000384468.2:p.Leu694del
ENST00000439117.6:c.*1380_*1382del ENSP00000406980.2:n.*1380_*1382del
ENST00000439673.6:c.1970_1972del ENSP00000399232.2:p.Leu657del
ENST00000563346.1:n.150_152del
ENST00000568454.5:c.2114_2116del ENSP00000454487.1:p.Leu705del
NM_000548.3:c.2081_2083del , LRG_487t1:c.2081_2083del NP_000539.2:p.Leu694del
NM_001077183.1:c.2081_2083del NP_001070651.1:p.Leu694del
NM_001114382.1:c.2081_2083del NP_001107854.1:p.Leu694del
XM_005255529.3:c.2081_2083del XP_005255586.2:p.Leu694del
XM_005255531.3:c.2081_2083del XP_005255588.2:p.Leu694del
XM_011522636.1:c.2081_2083del XP_011520938.1:p.Leu694del
XM_011522637.1:c.2081_2083del XP_011520939.1:p.Leu694del
XM_011522638.1:c.1970_1972del XP_011520940.1:p.Leu657del
XM_011522639.1:c.2081_2083del XP_011520941.1:p.Leu694del
XM_011522640.1:c.2081_2083del XP_011520942.1:p.Leu694del
XM_011522641.1:c.1970_1972del XP_011520943.1:p.Leu657del
NM_000548.4:c.2081_2083del NP_000539.2:p.Leu694del
NM_001077183.2:c.2081_2083del NP_001070651.1:p.Leu694del
NM_001114382.2:c.2081_2083del NP_001107854.1:p.Leu694del
NM_001318827.1:c.1970_1972del NP_001305756.1:p.Leu657del
NM_001318829.1:c.1934_1936del NP_001305758.1:p.Leu645del
NM_001318831.1:c.1481_1483del NP_001305760.1:p.Leu494del
NM_001318832.1:c.2114_2116del NP_001305761.1:p.Leu705del
NM_001363528.1:c.2081_2083del NP_001350457.1:p.Leu694del
NM_021055.2:c.2081_2083del NP_066399.2:p.Leu694del
XM_005255531.4:c.2081_2083del XP_005255588.2:p.Leu694del
XM_011522636.2:c.2081_2083del XP_011520938.1:p.Leu694del
XM_011522637.2:c.2081_2083del XP_011520939.1:p.Leu694del
XM_011522638.2:c.2243_2245del XP_011520940.2:p.Leu748del
XM_011522639.2:c.2081_2083del XP_011520941.1:p.Leu694del
XM_011522640.2:c.2081_2083del XP_011520942.1:p.Leu694del
XM_017023615.1:c.2081_2083del XP_016879104.1:p.Leu694del
XM_017023616.1:c.2081_2083del XP_016879105.1:p.Leu694del
XM_017023617.1:c.2243_2245del XP_016879106.1:p.Leu748del
XM_017023618.1:c.737_739del XP_016879107.1:p.Leu246del
XM_024450413.1:c.2081_2083del XP_024306181.1:p.Leu694del
NM_000548.5:c.2081_2083del MANE Select NP_000539.2:p.Leu694del
NM_001370404.1:c.2081_2083del NP_001357333.1:p.Leu694del
NM_001370405.1:c.2081_2083del NP_001357334.1:p.Leu694del
NM_001077183.3:c.2081_2083del NP_001070651.1:p.Leu694del
NM_001114382.3:c.2081_2083del NP_001107854.1:p.Leu694del
NM_001318827.2:c.1970_1972del NP_001305756.1:p.Leu657del
NM_001318829.2:c.1934_1936del NP_001305758.1:p.Leu645del
NM_001318831.2:c.1481_1483del NP_001305760.1:p.Leu494del
NM_001318832.2:c.2114_2116del NP_001305761.1:p.Leu705del
NM_001363528.2:c.2081_2083del NP_001350457.1:p.Leu694del
NM_021055.3:c.2081_2083del NP_066399.2:p.Leu694del