Canonical Allele Identifier: CA394314421
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151630716

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3565A>T ENSP00000455997.2:n.*3565A>T
ENST00000642206.2:c.5063A>T ENSP00000495146.2:p.Lys1688Met
ENST00000642365.2:c.5213A>T ENSP00000495459.2:p.Lys1738Met
ENST00000644417.2:c.*5729A>T ENSP00000493912.2:n.*5729A>T
ENST00000646464.2:c.*7965A>T ENSP00000496610.2:n.*7965A>T
ENST00000219476.9:c.5216A>T MANE Select ENSP00000219476.3:p.Lys1739Met
ENST00000350773.9:c.5147A>T ENSP00000344383.4:p.Lys1716Met
ENST00000401874.7:c.5015A>T ENSP00000384468.2:p.Lys1672Met
ENST00000568454.6:c.5048A>T ENSP00000454487.1:p.Lys1683Met
ENST00000569110.2:c.1439A>T
ENST00000569930.2:n.3098A>T
ENST00000642365.1:c.3870A>T
ENST00000642561.1:c.5075A>T ENSP00000495099.1:p.Lys1692Met
ENST00000642791.1:n.813A>T
ENST00000642797.1:c.5018A>T ENSP00000493846.1:p.Lys1673Met
ENST00000642936.1:c.5084A>T ENSP00000494514.1:p.Lys1695Met
ENST00000643088.1:c.5009A>T ENSP00000494747.1:p.Lys1670Met
ENST00000643426.1:n.2864A>T
ENST00000643946.1:c.5141A>T ENSP00000495927.1:p.Lys1714Met
ENST00000644043.1:c.5087A>T ENSP00000496262.1:p.Lys1696Met
ENST00000644329.1:c.5102A>T ENSP00000496611.1:p.Lys1701Met
ENST00000644335.1:c.5012A>T ENSP00000496317.1:p.Lys1671Met
ENST00000644399.1:c.5137A>T
ENST00000645024.1:n.3300A>T
ENST00000646388.1:c.5210A>T ENSP00000495921.1:p.Lys1737Met
ENST00000646634.1:n.4031A>T
ENST00000646674.1:n.2468A>T
ENST00000647042.1:n.2439A>T
ENST00000647180.1:n.2329A>T
ENST00000219476.7:c.5216A>T ENSP00000219476.3:p.Lys1739Met
ENST00000350773.8:c.5147A>T ENSP00000344383.4:p.Lys1716Met
ENST00000382538.10:c.4871A>T ENSP00000371978.6:p.Lys1624Met
ENST00000401874.6:c.5015A>T ENSP00000384468.2:p.Lys1672Met
ENST00000439117.6:c.*4383A>T ENSP00000406980.2:n.*4383A>T
ENST00000439673.6:c.4907A>T ENSP00000399232.2:p.Lys1636Met
ENST00000497886.5:n.2939A>T
ENST00000568454.5:c.5048A>T ENSP00000454487.1:p.Lys1683Met
ENST00000569110.1:c.1398A>T
ENST00000569930.1:n.2331A>T
NM_000548.3:c.5216A>T , LRG_487t1:c.5216A>T NP_000539.2:p.Lys1739Met
NM_001077183.1:c.5015A>T NP_001070651.1:p.Lys1672Met
NM_001114382.1:c.5147A>T NP_001107854.1:p.Lys1716Met
XM_005255529.3:c.5087A>T XP_005255586.2:p.Lys1696Met
XM_005255531.3:c.5018A>T XP_005255588.2:p.Lys1673Met
XM_011522636.1:c.5270A>T XP_011520938.1:p.Lys1757Met
XM_011522637.1:c.5267A>T XP_011520939.1:p.Lys1756Met
XM_011522638.1:c.5159A>T XP_011520940.1:p.Lys1720Met
XM_011522639.1:c.5141A>T XP_011520941.1:p.Lys1714Met
XM_011522640.1:c.5138A>T XP_011520942.1:p.Lys1713Met
XM_011522641.1:c.4907A>T XP_011520943.1:p.Lys1636Met
NM_000548.4:c.5216A>T NP_000539.2:p.Lys1739Met
NM_001077183.2:c.5015A>T NP_001070651.1:p.Lys1672Met
NM_001114382.2:c.5147A>T NP_001107854.1:p.Lys1716Met
NM_001318827.1:c.4907A>T NP_001305756.1:p.Lys1636Met
NM_001318829.1:c.4871A>T NP_001305758.1:p.Lys1624Met
NM_001318831.1:c.4484A>T NP_001305760.1:p.Lys1495Met
NM_001318832.1:c.5048A>T NP_001305761.1:p.Lys1683Met
NM_001363528.1:c.5018A>T NP_001350457.1:p.Lys1673Met
NM_021055.2:c.5087A>T NP_066399.2:p.Lys1696Met
XM_005255531.4:c.5018A>T XP_005255588.2:p.Lys1673Met
XM_011522636.2:c.5270A>T XP_011520938.1:p.Lys1757Met
XM_011522637.2:c.5267A>T XP_011520939.1:p.Lys1756Met
XM_011522638.2:c.5432A>T XP_011520940.2:p.Lys1811Met
XM_011522639.2:c.5141A>T XP_011520941.1:p.Lys1714Met
XM_011522640.2:c.5138A>T XP_011520942.1:p.Lys1713Met
XM_017023615.1:c.5213A>T XP_016879104.1:p.Lys1738Met
XM_017023616.1:c.5084A>T XP_016879105.1:p.Lys1695Met
XM_017023617.1:c.5180A>T XP_016879106.1:p.Lys1727Met
XM_017023618.1:c.3926A>T XP_016879107.1:p.Lys1309Met
XM_024450413.1:c.5102A>T XP_024306181.1:p.Lys1701Met
NM_000548.5:c.5216A>T MANE Select NP_000539.2:p.Lys1739Met
NM_001370404.1:c.5084A>T NP_001357333.1:p.Lys1695Met
NM_001370405.1:c.5075A>T NP_001357334.1:p.Lys1692Met
NM_001077183.3:c.5015A>T NP_001070651.1:p.Lys1672Met
NM_001114382.3:c.5147A>T NP_001107854.1:p.Lys1716Met
NM_001318827.2:c.4907A>T NP_001305756.1:p.Lys1636Met
NM_001318829.2:c.4871A>T NP_001305758.1:p.Lys1624Met
NM_001318831.2:c.4484A>T NP_001305760.1:p.Lys1495Met
NM_001318832.2:c.5048A>T NP_001305761.1:p.Lys1683Met
NM_001363528.2:c.5018A>T NP_001350457.1:p.Lys1673Met
NM_021055.3:c.5087A>T NP_066399.2:p.Lys1696Met