Canonical Allele Identifier: CA022490
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49373
ClinVar RCV Id: RCV000042633
dbSNP Id: rs137854228

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088594dup , CM000678.2:g.2088594dup GRCh38
NC_000016.9:g.2138595dup , CM000678.1:g.2138595dup GRCh37
NC_000016.8:g.2078596dup NCBI36
NG_005895.1:g.44289dup , LRG_487:g.44289dup
NG_008617.1:g.54628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3757dup ENSP00000455997.2:n.*3757dup
ENST00000642206.2:c.5255dup ENSP00000495146.2:p.Thr1753HisfsTer?
ENST00000642365.2:c.5405dup ENSP00000495459.2:p.Thr1803HisfsTer?
ENST00000644417.2:c.*5921dup ENSP00000493912.2:n.*5921dup
ENST00000646464.2:c.*8157dup ENSP00000496610.2:n.*8157dup
ENST00000219476.9:c.5408dup MANE Select ENSP00000219476.3:p.Thr1804HisfsTer?
ENST00000350773.9:c.5339dup ENSP00000344383.4:p.Thr1781HisfsTer?
ENST00000401874.7:c.5207dup ENSP00000384468.2:p.Thr1737HisfsTer?
ENST00000568454.6:c.5240dup ENSP00000454487.1:p.Thr1748HisfsTer?
ENST00000569110.2:c.1631dup
ENST00000569930.2:n.3290dup
ENST00000642365.1:c.4062dup
ENST00000642561.1:c.5267dup ENSP00000495099.1:p.Thr1757HisfsTer?
ENST00000642791.1:n.1005dup
ENST00000642797.1:c.5210dup ENSP00000493846.1:p.Thr1738HisfsTer?
ENST00000642936.1:c.5276dup ENSP00000494514.1:p.Thr1760HisfsTer?
ENST00000643088.1:c.5201dup ENSP00000494747.1:p.Thr1735HisfsTer?
ENST00000643426.1:n.3056dup
ENST00000643946.1:c.5333dup ENSP00000495927.1:p.Thr1779HisfsTer?
ENST00000644043.1:c.5279dup ENSP00000496262.1:p.Thr1761HisfsTer?
ENST00000644329.1:c.5294dup ENSP00000496611.1:p.Thr1766HisfsTer?
ENST00000644335.1:c.5204dup ENSP00000496317.1:p.Thr1736HisfsTer?
ENST00000644399.1:c.5329dup
ENST00000646388.1:c.5402dup ENSP00000495921.1:p.Thr1802HisfsTer?
ENST00000646634.1:n.4223dup
ENST00000646674.1:n.2660dup
ENST00000647042.1:n.2631dup
ENST00000647180.1:n.2521dup
ENST00000219476.7:c.5408dup ENSP00000219476.3:p.Thr1804HisfsTer?
ENST00000350773.8:c.5339dup ENSP00000344383.4:p.Thr1781HisfsTer?
ENST00000382538.10:c.5063dup ENSP00000371978.6:p.Thr1689HisfsTer?
ENST00000401874.6:c.5207dup ENSP00000384468.2:p.Thr1737HisfsTer?
ENST00000439117.6:c.*4575dup ENSP00000406980.2:n.*4575dup
ENST00000439673.6:c.5099dup ENSP00000399232.2:p.Thr1701HisfsTer?
ENST00000497886.5:n.3131dup
ENST00000568454.5:c.5240dup ENSP00000454487.1:p.Thr1748HisfsTer?
ENST00000569110.1:c.1590dup
ENST00000569930.1:n.2523dup
NM_000548.3:c.5408dup , LRG_487t1:c.5408dup NP_000539.2:p.Thr1804HisfsTer?
NM_001077183.1:c.5207dup NP_001070651.1:p.Thr1737HisfsTer?
NM_001114382.1:c.5339dup NP_001107854.1:p.Thr1781HisfsTer?
XM_005255529.3:c.5279dup XP_005255586.2:p.Thr1761HisfsTer?
XM_005255531.3:c.5210dup XP_005255588.2:p.Thr1738HisfsTer?
XM_011522636.1:c.5462dup XP_011520938.1:p.Thr1822HisfsTer?
XM_011522637.1:c.5459dup XP_011520939.1:p.Thr1821HisfsTer?
XM_011522638.1:c.5351dup XP_011520940.1:p.Thr1785HisfsTer?
XM_011522639.1:c.5333dup XP_011520941.1:p.Thr1779HisfsTer?
XM_011522640.1:c.5330dup XP_011520942.1:p.Thr1778HisfsTer?
XM_011522641.1:c.5099dup XP_011520943.1:p.Thr1701HisfsTer?
NM_000548.4:c.5408dup NP_000539.2:p.Thr1804HisfsTer?
NM_001077183.2:c.5207dup NP_001070651.1:p.Thr1737HisfsTer?
NM_001114382.2:c.5339dup NP_001107854.1:p.Thr1781HisfsTer?
NM_001318827.1:c.5099dup NP_001305756.1:p.Thr1701HisfsTer?
NM_001318829.1:c.5063dup NP_001305758.1:p.Thr1689HisfsTer?
NM_001318831.1:c.4676dup NP_001305760.1:p.Thr1560HisfsTer?
NM_001318832.1:c.5240dup NP_001305761.1:p.Thr1748HisfsTer?
NM_001363528.1:c.5210dup NP_001350457.1:p.Thr1738HisfsTer?
NM_021055.2:c.5279dup NP_066399.2:p.Thr1761HisfsTer?
XM_005255531.4:c.5210dup XP_005255588.2:p.Thr1738HisfsTer?
XM_011522636.2:c.5462dup XP_011520938.1:p.Thr1822HisfsTer?
XM_011522637.2:c.5459dup XP_011520939.1:p.Thr1821HisfsTer?
XM_011522638.2:c.5624dup XP_011520940.2:p.Thr1876HisfsTer?
XM_011522639.2:c.5333dup XP_011520941.1:p.Thr1779HisfsTer?
XM_011522640.2:c.5330dup XP_011520942.1:p.Thr1778HisfsTer?
XM_017023615.1:c.5405dup XP_016879104.1:p.Thr1803HisfsTer?
XM_017023616.1:c.5276dup XP_016879105.1:p.Thr1760HisfsTer?
XM_017023617.1:c.5372dup XP_016879106.1:p.Thr1792HisfsTer?
XM_017023618.1:c.4118dup XP_016879107.1:p.Thr1374HisfsTer?
XM_024450413.1:c.5294dup XP_024306181.1:p.Thr1766HisfsTer?
NM_000548.5:c.5408dup MANE Select NP_000539.2:p.Thr1804HisfsTer?
NM_001370404.1:c.5276dup NP_001357333.1:p.Thr1760HisfsTer?
NM_001370405.1:c.5267dup NP_001357334.1:p.Thr1757HisfsTer?
NM_001077183.3:c.5207dup NP_001070651.1:p.Thr1737HisfsTer?
NM_001114382.3:c.5339dup NP_001107854.1:p.Thr1781HisfsTer?
NM_001318827.2:c.5099dup NP_001305756.1:p.Thr1701HisfsTer?
NM_001318829.2:c.5063dup NP_001305758.1:p.Thr1689HisfsTer?
NM_001318831.2:c.4676dup NP_001305760.1:p.Thr1560HisfsTer?
NM_001318832.2:c.5240dup NP_001305761.1:p.Thr1748HisfsTer?
NM_001363528.2:c.5210dup NP_001350457.1:p.Thr1738HisfsTer?
NM_021055.3:c.5279dup NP_066399.2:p.Thr1761HisfsTer?