Canonical Allele Identifier: CA2202019279
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085263G= , CM000678.2:g.2085263G= GRCh38
NC_000016.9:g.2135264G= , CM000678.1:g.2135264G= GRCh37
NC_000016.8:g.2075265G= NCBI36
NG_005895.1:g.40958G= , LRG_487:g.40958G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2952G= ENSP00000455997.2:n.*2952G=
ENST00000642206.2:c.4450G= ENSP00000495146.2:p.Asp1484=
ENST00000642365.2:c.4600G= ENSP00000495459.2:p.Asp1534=
ENST00000644417.2:c.*4983G= ENSP00000493912.2:n.*4983G=
ENST00000646464.2:c.*7352G= ENSP00000496610.2:n.*7352G=
ENST00000219476.9:c.4603G= MANE Select ENSP00000219476.3:p.Asp1535=
ENST00000350773.9:c.4534G= ENSP00000344383.4:p.Asp1512=
ENST00000401874.7:c.4402G= ENSP00000384468.2:p.Asp1468=
ENST00000568454.6:c.4435G= ENSP00000454487.1:p.Asp1479=
ENST00000569110.2:c.826G=
ENST00000569930.2:n.2485G=
ENST00000642365.1:c.3257G=
ENST00000642561.1:c.4474G= ENSP00000495099.1:p.Asp1492=
ENST00000642728.1:n.785G=
ENST00000642791.1:n.200G=
ENST00000642797.1:c.4405G= ENSP00000493846.1:p.Asp1469=
ENST00000642936.1:c.4471G= ENSP00000494514.1:p.Asp1491=
ENST00000643088.1:c.4396G= ENSP00000494747.1:p.Asp1466=
ENST00000643177.1:n.617G=
ENST00000643426.1:n.2251G=
ENST00000643946.1:c.4528G= ENSP00000495927.1:p.Asp1510=
ENST00000644043.1:c.4474G= ENSP00000496262.1:p.Asp1492=
ENST00000644278.1:n.85G=
ENST00000644329.1:c.4402G= ENSP00000496611.1:p.Asp1468=
ENST00000644335.1:c.4399G= ENSP00000496317.1:p.Asp1467=
ENST00000644399.1:c.4524G=
ENST00000645024.1:n.2687G=
ENST00000646388.1:c.4597G= ENSP00000495921.1:p.Asp1533=
ENST00000646634.1:n.3418G=
ENST00000646674.1:n.1855G=
ENST00000647042.1:n.1826G=
ENST00000647180.1:n.1716G=
ENST00000219476.7:c.4603G= ENSP00000219476.3:p.Asp1535=
ENST00000350773.8:c.4534G= ENSP00000344383.4:p.Asp1512=
ENST00000382538.10:c.4258G= ENSP00000371978.6:p.Asp1420=
ENST00000401874.6:c.4402G= ENSP00000384468.2:p.Asp1468=
ENST00000439117.6:c.*3770G= ENSP00000406980.2:n.*3770G=
ENST00000439673.6:c.4294G= ENSP00000399232.2:p.Asp1432=
ENST00000497886.5:n.2361G=
ENST00000568454.5:c.4435G= ENSP00000454487.1:p.Asp1479=
ENST00000569110.1:c.785G=
ENST00000569930.1:n.1718G=
NM_000548.3:c.4603G= , LRG_487t1:c.4603G= NP_000539.2:p.Asp1535=
NM_001077183.1:c.4402G= NP_001070651.1:p.Asp1468=
NM_001114382.1:c.4534G= NP_001107854.1:p.Asp1512=
XM_005255529.3:c.4474G= XP_005255586.2:p.Asp1492=
XM_005255531.3:c.4405G= XP_005255588.2:p.Asp1469=
XM_011522636.1:c.4657G= XP_011520938.1:p.Asp1553=
XM_011522637.1:c.4654G= XP_011520939.1:p.Asp1552=
XM_011522638.1:c.4546G= XP_011520940.1:p.Asp1516=
XM_011522639.1:c.4528G= XP_011520941.1:p.Asp1510=
XM_011522640.1:c.4525G= XP_011520942.1:p.Asp1509=
XM_011522641.1:c.4294G= XP_011520943.1:p.Asp1432=
NM_000548.4:c.4603G= NP_000539.2:p.Asp1535=
NM_001077183.2:c.4402G= NP_001070651.1:p.Asp1468=
NM_001114382.2:c.4534G= NP_001107854.1:p.Asp1512=
NM_001318827.1:c.4294G= NP_001305756.1:p.Asp1432=
NM_001318829.1:c.4258G= NP_001305758.1:p.Asp1420=
NM_001318831.1:c.3871G= NP_001305760.1:p.Asp1291=
NM_001318832.1:c.4435G= NP_001305761.1:p.Asp1479=
NM_001363528.1:c.4405G= NP_001350457.1:p.Asp1469=
NM_021055.2:c.4474G= NP_066399.2:p.Asp1492=
XM_005255531.4:c.4405G= XP_005255588.2:p.Asp1469=
XM_011522636.2:c.4657G= XP_011520938.1:p.Asp1553=
XM_011522637.2:c.4654G= XP_011520939.1:p.Asp1552=
XM_011522638.2:c.4819G= XP_011520940.2:p.Asp1607=
XM_011522639.2:c.4528G= XP_011520941.1:p.Asp1510=
XM_011522640.2:c.4525G= XP_011520942.1:p.Asp1509=
XM_017023615.1:c.4600G= XP_016879104.1:p.Asp1534=
XM_017023616.1:c.4471G= XP_016879105.1:p.Asp1491=
XM_017023617.1:c.4567G= XP_016879106.1:p.Asp1523=
XM_017023618.1:c.3313G= XP_016879107.1:p.Asp1105=
XM_024450413.1:c.4402G= XP_024306181.1:p.Asp1468=
NM_000548.5:c.4603G= MANE Select NP_000539.2:p.Asp1535=
NM_001370404.1:c.4471G= NP_001357333.1:p.Asp1491=
NM_001370405.1:c.4474G= NP_001357334.1:p.Asp1492=
NM_001077183.3:c.4402G= NP_001070651.1:p.Asp1468=
NM_001114382.3:c.4534G= NP_001107854.1:p.Asp1512=
NM_001318827.2:c.4294G= NP_001305756.1:p.Asp1432=
NM_001318829.2:c.4258G= NP_001305758.1:p.Asp1420=
NM_001318831.2:c.3871G= NP_001305760.1:p.Asp1291=
NM_001318832.2:c.4435G= NP_001305761.1:p.Asp1479=
NM_001363528.2:c.4405G= NP_001350457.1:p.Asp1469=
NM_021055.3:c.4474G= NP_066399.2:p.Asp1492=