Canonical Allele Identifier: CA2202031712
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088247T= , CM000678.2:g.2088247T= GRCh38
NC_000016.9:g.2138248T= , CM000678.1:g.2138248T= GRCh37
NC_000016.8:g.2078249T= NCBI36
NG_005895.1:g.43942T= , LRG_487:g.43942T=
NG_008617.1:g.54974A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3530T= ENSP00000455997.2:n.*3530T=
ENST00000642206.2:c.5028T= ENSP00000495146.2:p.His1676=
ENST00000642365.2:c.5178T= ENSP00000495459.2:p.His1726=
ENST00000644417.2:c.*5694T= ENSP00000493912.2:n.*5694T=
ENST00000646464.2:c.*7930T= ENSP00000496610.2:n.*7930T=
ENST00000219476.9:c.5181T= MANE Select ENSP00000219476.3:p.His1727=
ENST00000350773.9:c.5112T= ENSP00000344383.4:p.His1704=
ENST00000401874.7:c.4980T= ENSP00000384468.2:p.His1660=
ENST00000568454.6:c.5013T= ENSP00000454487.1:p.His1671=
ENST00000569110.2:c.1404T=
ENST00000569930.2:n.3063T=
ENST00000642365.1:c.3835T=
ENST00000642561.1:c.5040T= ENSP00000495099.1:p.His1680=
ENST00000642791.1:n.778T=
ENST00000642797.1:c.4983T= ENSP00000493846.1:p.His1661=
ENST00000642936.1:c.5049T= ENSP00000494514.1:p.His1683=
ENST00000643088.1:c.4974T= ENSP00000494747.1:p.His1658=
ENST00000643426.1:n.2829T=
ENST00000643946.1:c.5106T= ENSP00000495927.1:p.His1702=
ENST00000644043.1:c.5052T= ENSP00000496262.1:p.His1684=
ENST00000644329.1:c.5067T= ENSP00000496611.1:p.His1689=
ENST00000644335.1:c.4977T= ENSP00000496317.1:p.His1659=
ENST00000644399.1:c.5102T=
ENST00000645024.1:n.3265T=
ENST00000646388.1:c.5175T= ENSP00000495921.1:p.His1725=
ENST00000646634.1:n.3996T=
ENST00000646674.1:n.2433T=
ENST00000647042.1:n.2404T=
ENST00000647180.1:n.2294T=
ENST00000219476.7:c.5181T= ENSP00000219476.3:p.His1727=
ENST00000350773.8:c.5112T= ENSP00000344383.4:p.His1704=
ENST00000382538.10:c.4836T= ENSP00000371978.6:p.His1612=
ENST00000401874.6:c.4980T= ENSP00000384468.2:p.His1660=
ENST00000439117.6:c.*4348T= ENSP00000406980.2:n.*4348T=
ENST00000439673.6:c.4872T= ENSP00000399232.2:p.His1624=
ENST00000497886.5:n.2904T=
ENST00000568454.5:c.5013T= ENSP00000454487.1:p.His1671=
ENST00000569110.1:c.1363T=
ENST00000569930.1:n.2296T=
NM_000548.3:c.5181T= , LRG_487t1:c.5181T= NP_000539.2:p.His1727=
NM_001077183.1:c.4980T= NP_001070651.1:p.His1660=
NM_001114382.1:c.5112T= NP_001107854.1:p.His1704=
XM_005255529.3:c.5052T= XP_005255586.2:p.His1684=
XM_005255531.3:c.4983T= XP_005255588.2:p.His1661=
XM_011522636.1:c.5235T= XP_011520938.1:p.His1745=
XM_011522637.1:c.5232T= XP_011520939.1:p.His1744=
XM_011522638.1:c.5124T= XP_011520940.1:p.His1708=
XM_011522639.1:c.5106T= XP_011520941.1:p.His1702=
XM_011522640.1:c.5103T= XP_011520942.1:p.His1701=
XM_011522641.1:c.4872T= XP_011520943.1:p.His1624=
NM_000548.4:c.5181T= NP_000539.2:p.His1727=
NM_001077183.2:c.4980T= NP_001070651.1:p.His1660=
NM_001114382.2:c.5112T= NP_001107854.1:p.His1704=
NM_001318827.1:c.4872T= NP_001305756.1:p.His1624=
NM_001318829.1:c.4836T= NP_001305758.1:p.His1612=
NM_001318831.1:c.4449T= NP_001305760.1:p.His1483=
NM_001318832.1:c.5013T= NP_001305761.1:p.His1671=
NM_001363528.1:c.4983T= NP_001350457.1:p.His1661=
NM_021055.2:c.5052T= NP_066399.2:p.His1684=
XM_005255531.4:c.4983T= XP_005255588.2:p.His1661=
XM_011522636.2:c.5235T= XP_011520938.1:p.His1745=
XM_011522637.2:c.5232T= XP_011520939.1:p.His1744=
XM_011522638.2:c.5397T= XP_011520940.2:p.His1799=
XM_011522639.2:c.5106T= XP_011520941.1:p.His1702=
XM_011522640.2:c.5103T= XP_011520942.1:p.His1701=
XM_017023615.1:c.5178T= XP_016879104.1:p.His1726=
XM_017023616.1:c.5049T= XP_016879105.1:p.His1683=
XM_017023617.1:c.5145T= XP_016879106.1:p.His1715=
XM_017023618.1:c.3891T= XP_016879107.1:p.His1297=
XM_024450413.1:c.5067T= XP_024306181.1:p.His1689=
NM_000548.5:c.5181T= MANE Select NP_000539.2:p.His1727=
NM_001370404.1:c.5049T= NP_001357333.1:p.His1683=
NM_001370405.1:c.5040T= NP_001357334.1:p.His1680=
NM_001077183.3:c.4980T= NP_001070651.1:p.His1660=
NM_001114382.3:c.5112T= NP_001107854.1:p.His1704=
NM_001318827.2:c.4872T= NP_001305756.1:p.His1624=
NM_001318829.2:c.4836T= NP_001305758.1:p.His1612=
NM_001318831.2:c.4449T= NP_001305760.1:p.His1483=
NM_001318832.2:c.5013T= NP_001305761.1:p.His1671=
NM_001363528.2:c.4983T= NP_001350457.1:p.His1661=
NM_021055.3:c.5052T= NP_066399.2:p.His1684=