Canonical Allele Identifier: CA394314418
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058272
ClinVar RCV Id: RCV001367386
dbSNP Id: rs2151630716

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088282A>C , CM000678.2:g.2088282A>C GRCh38
NC_000016.9:g.2138283A>C , CM000678.1:g.2138283A>C GRCh37
NC_000016.8:g.2078284A>C NCBI36
NG_005895.1:g.43977A>C , LRG_487:g.43977A>C
NG_008617.1:g.54939T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3565A>C ENSP00000455997.2:n.*3565A>C
ENST00000642206.2:c.5063A>C ENSP00000495146.2:p.Lys1688Thr
ENST00000642365.2:c.5213A>C ENSP00000495459.2:p.Lys1738Thr
ENST00000644417.2:c.*5729A>C ENSP00000493912.2:n.*5729A>C
ENST00000646464.2:c.*7965A>C ENSP00000496610.2:n.*7965A>C
ENST00000219476.9:c.5216A>C MANE Select ENSP00000219476.3:p.Lys1739Thr
ENST00000350773.9:c.5147A>C ENSP00000344383.4:p.Lys1716Thr
ENST00000401874.7:c.5015A>C ENSP00000384468.2:p.Lys1672Thr
ENST00000568454.6:c.5048A>C ENSP00000454487.1:p.Lys1683Thr
ENST00000569110.2:c.1439A>C
ENST00000569930.2:n.3098A>C
ENST00000642365.1:c.3870A>C
ENST00000642561.1:c.5075A>C ENSP00000495099.1:p.Lys1692Thr
ENST00000642791.1:n.813A>C
ENST00000642797.1:c.5018A>C ENSP00000493846.1:p.Lys1673Thr
ENST00000642936.1:c.5084A>C ENSP00000494514.1:p.Lys1695Thr
ENST00000643088.1:c.5009A>C ENSP00000494747.1:p.Lys1670Thr
ENST00000643426.1:n.2864A>C
ENST00000643946.1:c.5141A>C ENSP00000495927.1:p.Lys1714Thr
ENST00000644043.1:c.5087A>C ENSP00000496262.1:p.Lys1696Thr
ENST00000644329.1:c.5102A>C ENSP00000496611.1:p.Lys1701Thr
ENST00000644335.1:c.5012A>C ENSP00000496317.1:p.Lys1671Thr
ENST00000644399.1:c.5137A>C
ENST00000645024.1:n.3300A>C
ENST00000646388.1:c.5210A>C ENSP00000495921.1:p.Lys1737Thr
ENST00000646634.1:n.4031A>C
ENST00000646674.1:n.2468A>C
ENST00000647042.1:n.2439A>C
ENST00000647180.1:n.2329A>C
ENST00000219476.7:c.5216A>C ENSP00000219476.3:p.Lys1739Thr
ENST00000350773.8:c.5147A>C ENSP00000344383.4:p.Lys1716Thr
ENST00000382538.10:c.4871A>C ENSP00000371978.6:p.Lys1624Thr
ENST00000401874.6:c.5015A>C ENSP00000384468.2:p.Lys1672Thr
ENST00000439117.6:c.*4383A>C ENSP00000406980.2:n.*4383A>C
ENST00000439673.6:c.4907A>C ENSP00000399232.2:p.Lys1636Thr
ENST00000497886.5:n.2939A>C
ENST00000568454.5:c.5048A>C ENSP00000454487.1:p.Lys1683Thr
ENST00000569110.1:c.1398A>C
ENST00000569930.1:n.2331A>C
NM_000548.3:c.5216A>C , LRG_487t1:c.5216A>C NP_000539.2:p.Lys1739Thr
NM_001077183.1:c.5015A>C NP_001070651.1:p.Lys1672Thr
NM_001114382.1:c.5147A>C NP_001107854.1:p.Lys1716Thr
XM_005255529.3:c.5087A>C XP_005255586.2:p.Lys1696Thr
XM_005255531.3:c.5018A>C XP_005255588.2:p.Lys1673Thr
XM_011522636.1:c.5270A>C XP_011520938.1:p.Lys1757Thr
XM_011522637.1:c.5267A>C XP_011520939.1:p.Lys1756Thr
XM_011522638.1:c.5159A>C XP_011520940.1:p.Lys1720Thr
XM_011522639.1:c.5141A>C XP_011520941.1:p.Lys1714Thr
XM_011522640.1:c.5138A>C XP_011520942.1:p.Lys1713Thr
XM_011522641.1:c.4907A>C XP_011520943.1:p.Lys1636Thr
NM_000548.4:c.5216A>C NP_000539.2:p.Lys1739Thr
NM_001077183.2:c.5015A>C NP_001070651.1:p.Lys1672Thr
NM_001114382.2:c.5147A>C NP_001107854.1:p.Lys1716Thr
NM_001318827.1:c.4907A>C NP_001305756.1:p.Lys1636Thr
NM_001318829.1:c.4871A>C NP_001305758.1:p.Lys1624Thr
NM_001318831.1:c.4484A>C NP_001305760.1:p.Lys1495Thr
NM_001318832.1:c.5048A>C NP_001305761.1:p.Lys1683Thr
NM_001363528.1:c.5018A>C NP_001350457.1:p.Lys1673Thr
NM_021055.2:c.5087A>C NP_066399.2:p.Lys1696Thr
XM_005255531.4:c.5018A>C XP_005255588.2:p.Lys1673Thr
XM_011522636.2:c.5270A>C XP_011520938.1:p.Lys1757Thr
XM_011522637.2:c.5267A>C XP_011520939.1:p.Lys1756Thr
XM_011522638.2:c.5432A>C XP_011520940.2:p.Lys1811Thr
XM_011522639.2:c.5141A>C XP_011520941.1:p.Lys1714Thr
XM_011522640.2:c.5138A>C XP_011520942.1:p.Lys1713Thr
XM_017023615.1:c.5213A>C XP_016879104.1:p.Lys1738Thr
XM_017023616.1:c.5084A>C XP_016879105.1:p.Lys1695Thr
XM_017023617.1:c.5180A>C XP_016879106.1:p.Lys1727Thr
XM_017023618.1:c.3926A>C XP_016879107.1:p.Lys1309Thr
XM_024450413.1:c.5102A>C XP_024306181.1:p.Lys1701Thr
NM_000548.5:c.5216A>C MANE Select NP_000539.2:p.Lys1739Thr
NM_001370404.1:c.5084A>C NP_001357333.1:p.Lys1695Thr
NM_001370405.1:c.5075A>C NP_001357334.1:p.Lys1692Thr
NM_001077183.3:c.5015A>C NP_001070651.1:p.Lys1672Thr
NM_001114382.3:c.5147A>C NP_001107854.1:p.Lys1716Thr
NM_001318827.2:c.4907A>C NP_001305756.1:p.Lys1636Thr
NM_001318829.2:c.4871A>C NP_001305758.1:p.Lys1624Thr
NM_001318831.2:c.4484A>C NP_001305760.1:p.Lys1495Thr
NM_001318832.2:c.5048A>C NP_001305761.1:p.Lys1683Thr
NM_001363528.2:c.5018A>C NP_001350457.1:p.Lys1673Thr
NM_021055.3:c.5087A>C NP_066399.2:p.Lys1696Thr