Canonical Allele Identifier: CA2202019291
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085264A= , CM000678.2:g.2085264A= GRCh38
NC_000016.9:g.2135265A= , CM000678.1:g.2135265A= GRCh37
NC_000016.8:g.2075266A= NCBI36
NG_005895.1:g.40959A= , LRG_487:g.40959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2953A= ENSP00000455997.2:n.*2953A=
ENST00000642206.2:c.4451A= ENSP00000495146.2:p.Asp1484=
ENST00000642365.2:c.4601A= ENSP00000495459.2:p.Asp1534=
ENST00000644417.2:c.*4984A= ENSP00000493912.2:n.*4984A=
ENST00000646464.2:c.*7353A= ENSP00000496610.2:n.*7353A=
ENST00000219476.9:c.4604A= MANE Select ENSP00000219476.3:p.Asp1535=
ENST00000350773.9:c.4535A= ENSP00000344383.4:p.Asp1512=
ENST00000401874.7:c.4403A= ENSP00000384468.2:p.Asp1468=
ENST00000568454.6:c.4436A= ENSP00000454487.1:p.Asp1479=
ENST00000569110.2:c.827A=
ENST00000569930.2:n.2486A=
ENST00000642365.1:c.3258A=
ENST00000642561.1:c.4475A= ENSP00000495099.1:p.Asp1492=
ENST00000642728.1:n.786A=
ENST00000642791.1:n.201A=
ENST00000642797.1:c.4406A= ENSP00000493846.1:p.Asp1469=
ENST00000642936.1:c.4472A= ENSP00000494514.1:p.Asp1491=
ENST00000643088.1:c.4397A= ENSP00000494747.1:p.Asp1466=
ENST00000643177.1:n.618A=
ENST00000643426.1:n.2252A=
ENST00000643946.1:c.4529A= ENSP00000495927.1:p.Asp1510=
ENST00000644043.1:c.4475A= ENSP00000496262.1:p.Asp1492=
ENST00000644278.1:n.86A=
ENST00000644329.1:c.4403A= ENSP00000496611.1:p.Asp1468=
ENST00000644335.1:c.4400A= ENSP00000496317.1:p.Asp1467=
ENST00000644399.1:c.4525A=
ENST00000645024.1:n.2688A=
ENST00000646388.1:c.4598A= ENSP00000495921.1:p.Asp1533=
ENST00000646634.1:n.3419A=
ENST00000646674.1:n.1856A=
ENST00000647042.1:n.1827A=
ENST00000647180.1:n.1717A=
ENST00000219476.7:c.4604A= ENSP00000219476.3:p.Asp1535=
ENST00000350773.8:c.4535A= ENSP00000344383.4:p.Asp1512=
ENST00000382538.10:c.4259A= ENSP00000371978.6:p.Asp1420=
ENST00000401874.6:c.4403A= ENSP00000384468.2:p.Asp1468=
ENST00000439117.6:c.*3771A= ENSP00000406980.2:n.*3771A=
ENST00000439673.6:c.4295A= ENSP00000399232.2:p.Asp1432=
ENST00000497886.5:n.2362A=
ENST00000568454.5:c.4436A= ENSP00000454487.1:p.Asp1479=
ENST00000569110.1:c.786A=
ENST00000569930.1:n.1719A=
NM_000548.3:c.4604A= , LRG_487t1:c.4604A= NP_000539.2:p.Asp1535=
NM_001077183.1:c.4403A= NP_001070651.1:p.Asp1468=
NM_001114382.1:c.4535A= NP_001107854.1:p.Asp1512=
XM_005255529.3:c.4475A= XP_005255586.2:p.Asp1492=
XM_005255531.3:c.4406A= XP_005255588.2:p.Asp1469=
XM_011522636.1:c.4658A= XP_011520938.1:p.Asp1553=
XM_011522637.1:c.4655A= XP_011520939.1:p.Asp1552=
XM_011522638.1:c.4547A= XP_011520940.1:p.Asp1516=
XM_011522639.1:c.4529A= XP_011520941.1:p.Asp1510=
XM_011522640.1:c.4526A= XP_011520942.1:p.Asp1509=
XM_011522641.1:c.4295A= XP_011520943.1:p.Asp1432=
NM_000548.4:c.4604A= NP_000539.2:p.Asp1535=
NM_001077183.2:c.4403A= NP_001070651.1:p.Asp1468=
NM_001114382.2:c.4535A= NP_001107854.1:p.Asp1512=
NM_001318827.1:c.4295A= NP_001305756.1:p.Asp1432=
NM_001318829.1:c.4259A= NP_001305758.1:p.Asp1420=
NM_001318831.1:c.3872A= NP_001305760.1:p.Asp1291=
NM_001318832.1:c.4436A= NP_001305761.1:p.Asp1479=
NM_001363528.1:c.4406A= NP_001350457.1:p.Asp1469=
NM_021055.2:c.4475A= NP_066399.2:p.Asp1492=
XM_005255531.4:c.4406A= XP_005255588.2:p.Asp1469=
XM_011522636.2:c.4658A= XP_011520938.1:p.Asp1553=
XM_011522637.2:c.4655A= XP_011520939.1:p.Asp1552=
XM_011522638.2:c.4820A= XP_011520940.2:p.Asp1607=
XM_011522639.2:c.4529A= XP_011520941.1:p.Asp1510=
XM_011522640.2:c.4526A= XP_011520942.1:p.Asp1509=
XM_017023615.1:c.4601A= XP_016879104.1:p.Asp1534=
XM_017023616.1:c.4472A= XP_016879105.1:p.Asp1491=
XM_017023617.1:c.4568A= XP_016879106.1:p.Asp1523=
XM_017023618.1:c.3314A= XP_016879107.1:p.Asp1105=
XM_024450413.1:c.4403A= XP_024306181.1:p.Asp1468=
NM_000548.5:c.4604A= MANE Select NP_000539.2:p.Asp1535=
NM_001370404.1:c.4472A= NP_001357333.1:p.Asp1491=
NM_001370405.1:c.4475A= NP_001357334.1:p.Asp1492=
NM_001077183.3:c.4403A= NP_001070651.1:p.Asp1468=
NM_001114382.3:c.4535A= NP_001107854.1:p.Asp1512=
NM_001318827.2:c.4295A= NP_001305756.1:p.Asp1432=
NM_001318829.2:c.4259A= NP_001305758.1:p.Asp1420=
NM_001318831.2:c.3872A= NP_001305760.1:p.Asp1291=
NM_001318832.2:c.4436A= NP_001305761.1:p.Asp1479=
NM_001363528.2:c.4406A= NP_001350457.1:p.Asp1469=
NM_021055.3:c.4475A= NP_066399.2:p.Asp1492=