Canonical Allele Identifier: CA2202019701
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085314G= , CM000678.2:g.2085314G= GRCh38
NC_000016.9:g.2135315G= , CM000678.1:g.2135315G= GRCh37
NC_000016.8:g.2075316G= NCBI36
NG_005895.1:g.41009G= , LRG_487:g.41009G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3003G= ENSP00000455997.2:n.*3003G=
ENST00000642206.2:c.4501G= ENSP00000495146.2:p.Glu1501=
ENST00000642365.2:c.4651G= ENSP00000495459.2:p.Glu1551=
ENST00000644417.2:c.*5034G= ENSP00000493912.2:n.*5034G=
ENST00000646464.2:c.*7403G= ENSP00000496610.2:n.*7403G=
ENST00000219476.9:c.4654G= MANE Select ENSP00000219476.3:p.Glu1552=
ENST00000350773.9:c.4585G= ENSP00000344383.4:p.Glu1529=
ENST00000401874.7:c.4453G= ENSP00000384468.2:p.Glu1485=
ENST00000568454.6:c.4486G= ENSP00000454487.1:p.Glu1496=
ENST00000569110.2:c.877G=
ENST00000569930.2:n.2536G=
ENST00000642365.1:c.3308G=
ENST00000642561.1:c.4525G= ENSP00000495099.1:p.Glu1509=
ENST00000642728.1:n.836G=
ENST00000642791.1:n.251G=
ENST00000642797.1:c.4456G= ENSP00000493846.1:p.Glu1486=
ENST00000642936.1:c.4522G= ENSP00000494514.1:p.Glu1508=
ENST00000643088.1:c.4447G= ENSP00000494747.1:p.Glu1483=
ENST00000643177.1:n.668G=
ENST00000643426.1:n.2302G=
ENST00000643946.1:c.4579G= ENSP00000495927.1:p.Glu1527=
ENST00000644043.1:c.4525G= ENSP00000496262.1:p.Glu1509=
ENST00000644278.1:n.136G=
ENST00000644329.1:c.4453G= ENSP00000496611.1:p.Glu1485=
ENST00000644335.1:c.4450G= ENSP00000496317.1:p.Glu1484=
ENST00000644399.1:c.4575G=
ENST00000645024.1:n.2738G=
ENST00000646388.1:c.4648G= ENSP00000495921.1:p.Glu1550=
ENST00000646634.1:n.3469G=
ENST00000646674.1:n.1906G=
ENST00000647042.1:n.1877G=
ENST00000647180.1:n.1767G=
ENST00000219476.7:c.4654G= ENSP00000219476.3:p.Glu1552=
ENST00000350773.8:c.4585G= ENSP00000344383.4:p.Glu1529=
ENST00000382538.10:c.4309G= ENSP00000371978.6:p.Glu1437=
ENST00000401874.6:c.4453G= ENSP00000384468.2:p.Glu1485=
ENST00000439117.6:c.*3821G= ENSP00000406980.2:n.*3821G=
ENST00000439673.6:c.4345G= ENSP00000399232.2:p.Glu1449=
ENST00000497886.5:n.2412G=
ENST00000568454.5:c.4486G= ENSP00000454487.1:p.Glu1496=
ENST00000569110.1:c.836G=
ENST00000569930.1:n.1769G=
NM_000548.3:c.4654G= , LRG_487t1:c.4654G= NP_000539.2:p.Glu1552=
NM_001077183.1:c.4453G= NP_001070651.1:p.Glu1485=
NM_001114382.1:c.4585G= NP_001107854.1:p.Glu1529=
XM_005255529.3:c.4525G= XP_005255586.2:p.Glu1509=
XM_005255531.3:c.4456G= XP_005255588.2:p.Glu1486=
XM_011522636.1:c.4708G= XP_011520938.1:p.Glu1570=
XM_011522637.1:c.4705G= XP_011520939.1:p.Glu1569=
XM_011522638.1:c.4597G= XP_011520940.1:p.Glu1533=
XM_011522639.1:c.4579G= XP_011520941.1:p.Glu1527=
XM_011522640.1:c.4576G= XP_011520942.1:p.Glu1526=
XM_011522641.1:c.4345G= XP_011520943.1:p.Glu1449=
NM_000548.4:c.4654G= NP_000539.2:p.Glu1552=
NM_001077183.2:c.4453G= NP_001070651.1:p.Glu1485=
NM_001114382.2:c.4585G= NP_001107854.1:p.Glu1529=
NM_001318827.1:c.4345G= NP_001305756.1:p.Glu1449=
NM_001318829.1:c.4309G= NP_001305758.1:p.Glu1437=
NM_001318831.1:c.3922G= NP_001305760.1:p.Glu1308=
NM_001318832.1:c.4486G= NP_001305761.1:p.Glu1496=
NM_001363528.1:c.4456G= NP_001350457.1:p.Glu1486=
NM_021055.2:c.4525G= NP_066399.2:p.Glu1509=
XM_005255531.4:c.4456G= XP_005255588.2:p.Glu1486=
XM_011522636.2:c.4708G= XP_011520938.1:p.Glu1570=
XM_011522637.2:c.4705G= XP_011520939.1:p.Glu1569=
XM_011522638.2:c.4870G= XP_011520940.2:p.Glu1624=
XM_011522639.2:c.4579G= XP_011520941.1:p.Glu1527=
XM_011522640.2:c.4576G= XP_011520942.1:p.Glu1526=
XM_017023615.1:c.4651G= XP_016879104.1:p.Glu1551=
XM_017023616.1:c.4522G= XP_016879105.1:p.Glu1508=
XM_017023617.1:c.4618G= XP_016879106.1:p.Glu1540=
XM_017023618.1:c.3364G= XP_016879107.1:p.Glu1122=
XM_024450413.1:c.4453G= XP_024306181.1:p.Glu1485=
NM_000548.5:c.4654G= MANE Select NP_000539.2:p.Glu1552=
NM_001370404.1:c.4522G= NP_001357333.1:p.Glu1508=
NM_001370405.1:c.4525G= NP_001357334.1:p.Glu1509=
NM_001077183.3:c.4453G= NP_001070651.1:p.Glu1485=
NM_001114382.3:c.4585G= NP_001107854.1:p.Glu1529=
NM_001318827.2:c.4345G= NP_001305756.1:p.Glu1449=
NM_001318829.2:c.4309G= NP_001305758.1:p.Glu1437=
NM_001318831.2:c.3922G= NP_001305760.1:p.Glu1308=
NM_001318832.2:c.4486G= NP_001305761.1:p.Glu1496=
NM_001363528.2:c.4456G= NP_001350457.1:p.Glu1486=
NM_021055.3:c.4525G= NP_066399.2:p.Glu1509=