Canonical Allele Identifier: CA2202031937
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088266G= , CM000678.2:g.2088266G= GRCh38
NC_000016.9:g.2138267G= , CM000678.1:g.2138267G= GRCh37
NC_000016.8:g.2078268G= NCBI36
NG_005895.1:g.43961G= , LRG_487:g.43961G=
NG_008617.1:g.54955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3549G= ENSP00000455997.2:n.*3549G=
ENST00000642206.2:c.5047G= ENSP00000495146.2:p.Asp1683=
ENST00000642365.2:c.5197G= ENSP00000495459.2:p.Asp1733=
ENST00000644417.2:c.*5713G= ENSP00000493912.2:n.*5713G=
ENST00000646464.2:c.*7949G= ENSP00000496610.2:n.*7949G=
ENST00000219476.9:c.5200G= MANE Select ENSP00000219476.3:p.Asp1734=
ENST00000350773.9:c.5131G= ENSP00000344383.4:p.Asp1711=
ENST00000401874.7:c.4999G= ENSP00000384468.2:p.Asp1667=
ENST00000568454.6:c.5032G= ENSP00000454487.1:p.Asp1678=
ENST00000569110.2:c.1423G=
ENST00000569930.2:n.3082G=
ENST00000642365.1:c.3854G=
ENST00000642561.1:c.5059G= ENSP00000495099.1:p.Asp1687=
ENST00000642791.1:n.797G=
ENST00000642797.1:c.5002G= ENSP00000493846.1:p.Asp1668=
ENST00000642936.1:c.5068G= ENSP00000494514.1:p.Asp1690=
ENST00000643088.1:c.4993G= ENSP00000494747.1:p.Asp1665=
ENST00000643426.1:n.2848G=
ENST00000643946.1:c.5125G= ENSP00000495927.1:p.Asp1709=
ENST00000644043.1:c.5071G= ENSP00000496262.1:p.Asp1691=
ENST00000644329.1:c.5086G= ENSP00000496611.1:p.Asp1696=
ENST00000644335.1:c.4996G= ENSP00000496317.1:p.Asp1666=
ENST00000644399.1:c.5121G=
ENST00000645024.1:n.3284G=
ENST00000646388.1:c.5194G= ENSP00000495921.1:p.Asp1732=
ENST00000646634.1:n.4015G=
ENST00000646674.1:n.2452G=
ENST00000647042.1:n.2423G=
ENST00000647180.1:n.2313G=
ENST00000219476.7:c.5200G= ENSP00000219476.3:p.Asp1734=
ENST00000350773.8:c.5131G= ENSP00000344383.4:p.Asp1711=
ENST00000382538.10:c.4855G= ENSP00000371978.6:p.Asp1619=
ENST00000401874.6:c.4999G= ENSP00000384468.2:p.Asp1667=
ENST00000439117.6:c.*4367G= ENSP00000406980.2:n.*4367G=
ENST00000439673.6:c.4891G= ENSP00000399232.2:p.Asp1631=
ENST00000497886.5:n.2923G=
ENST00000568454.5:c.5032G= ENSP00000454487.1:p.Asp1678=
ENST00000569110.1:c.1382G=
ENST00000569930.1:n.2315G=
NM_000548.3:c.5200G= , LRG_487t1:c.5200G= NP_000539.2:p.Asp1734=
NM_001077183.1:c.4999G= NP_001070651.1:p.Asp1667=
NM_001114382.1:c.5131G= NP_001107854.1:p.Asp1711=
XM_005255529.3:c.5071G= XP_005255586.2:p.Asp1691=
XM_005255531.3:c.5002G= XP_005255588.2:p.Asp1668=
XM_011522636.1:c.5254G= XP_011520938.1:p.Asp1752=
XM_011522637.1:c.5251G= XP_011520939.1:p.Asp1751=
XM_011522638.1:c.5143G= XP_011520940.1:p.Asp1715=
XM_011522639.1:c.5125G= XP_011520941.1:p.Asp1709=
XM_011522640.1:c.5122G= XP_011520942.1:p.Asp1708=
XM_011522641.1:c.4891G= XP_011520943.1:p.Asp1631=
NM_000548.4:c.5200G= NP_000539.2:p.Asp1734=
NM_001077183.2:c.4999G= NP_001070651.1:p.Asp1667=
NM_001114382.2:c.5131G= NP_001107854.1:p.Asp1711=
NM_001318827.1:c.4891G= NP_001305756.1:p.Asp1631=
NM_001318829.1:c.4855G= NP_001305758.1:p.Asp1619=
NM_001318831.1:c.4468G= NP_001305760.1:p.Asp1490=
NM_001318832.1:c.5032G= NP_001305761.1:p.Asp1678=
NM_001363528.1:c.5002G= NP_001350457.1:p.Asp1668=
NM_021055.2:c.5071G= NP_066399.2:p.Asp1691=
XM_005255531.4:c.5002G= XP_005255588.2:p.Asp1668=
XM_011522636.2:c.5254G= XP_011520938.1:p.Asp1752=
XM_011522637.2:c.5251G= XP_011520939.1:p.Asp1751=
XM_011522638.2:c.5416G= XP_011520940.2:p.Asp1806=
XM_011522639.2:c.5125G= XP_011520941.1:p.Asp1709=
XM_011522640.2:c.5122G= XP_011520942.1:p.Asp1708=
XM_017023615.1:c.5197G= XP_016879104.1:p.Asp1733=
XM_017023616.1:c.5068G= XP_016879105.1:p.Asp1690=
XM_017023617.1:c.5164G= XP_016879106.1:p.Asp1722=
XM_017023618.1:c.3910G= XP_016879107.1:p.Asp1304=
XM_024450413.1:c.5086G= XP_024306181.1:p.Asp1696=
NM_000548.5:c.5200G= MANE Select NP_000539.2:p.Asp1734=
NM_001370404.1:c.5068G= NP_001357333.1:p.Asp1690=
NM_001370405.1:c.5059G= NP_001357334.1:p.Asp1687=
NM_001077183.3:c.4999G= NP_001070651.1:p.Asp1667=
NM_001114382.3:c.5131G= NP_001107854.1:p.Asp1711=
NM_001318827.2:c.4891G= NP_001305756.1:p.Asp1631=
NM_001318829.2:c.4855G= NP_001305758.1:p.Asp1619=
NM_001318831.2:c.4468G= NP_001305760.1:p.Asp1490=
NM_001318832.2:c.5032G= NP_001305761.1:p.Asp1678=
NM_001363528.2:c.5002G= NP_001350457.1:p.Asp1668=
NM_021055.3:c.5071G= NP_066399.2:p.Asp1691=