Canonical Allele Identifier: CA2202031638
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088238G= , CM000678.2:g.2088238G= GRCh38
NC_000016.9:g.2138239G= , CM000678.1:g.2138239G= GRCh37
NC_000016.8:g.2078240G= NCBI36
NG_005895.1:g.43933G= , LRG_487:g.43933G=
NG_008617.1:g.54983C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3521G= ENSP00000455997.2:n.*3521G=
ENST00000642206.2:c.5019G= ENSP00000495146.2:p.Gln1673=
ENST00000642365.2:c.5169G= ENSP00000495459.2:p.Gln1723=
ENST00000644417.2:c.*5685G= ENSP00000493912.2:n.*5685G=
ENST00000646464.2:c.*7921G= ENSP00000496610.2:n.*7921G=
ENST00000219476.9:c.5172G= MANE Select ENSP00000219476.3:p.Gln1724=
ENST00000350773.9:c.5103G= ENSP00000344383.4:p.Gln1701=
ENST00000401874.7:c.4971G= ENSP00000384468.2:p.Gln1657=
ENST00000568454.6:c.5004G= ENSP00000454487.1:p.Gln1668=
ENST00000569110.2:c.1395G=
ENST00000569930.2:n.3054G=
ENST00000642365.1:c.3826G=
ENST00000642561.1:c.5032-1G= ENSP00000495099.1:n.5032-1G=
ENST00000642791.1:n.769G=
ENST00000642797.1:c.4974G= ENSP00000493846.1:p.Gln1658=
ENST00000642936.1:c.5040G= ENSP00000494514.1:p.Gln1680=
ENST00000643088.1:c.4965G= ENSP00000494747.1:p.Gln1655=
ENST00000643426.1:n.2820G=
ENST00000643946.1:c.5097G= ENSP00000495927.1:p.Gln1699=
ENST00000644043.1:c.5043G= ENSP00000496262.1:p.Gln1681=
ENST00000644329.1:c.5058G= ENSP00000496611.1:p.Gln1686=
ENST00000644335.1:c.4968G= ENSP00000496317.1:p.Gln1656=
ENST00000644399.1:c.5093G=
ENST00000645024.1:n.3256G=
ENST00000646388.1:c.5166G= ENSP00000495921.1:p.Gln1722=
ENST00000646634.1:n.3987G=
ENST00000646674.1:n.2424G=
ENST00000647042.1:n.2395G=
ENST00000647180.1:n.2285G=
ENST00000219476.7:c.5172G= ENSP00000219476.3:p.Gln1724=
ENST00000350773.8:c.5103G= ENSP00000344383.4:p.Gln1701=
ENST00000382538.10:c.4827G= ENSP00000371978.6:p.Gln1609=
ENST00000401874.6:c.4971G= ENSP00000384468.2:p.Gln1657=
ENST00000439117.6:c.*4339G= ENSP00000406980.2:n.*4339G=
ENST00000439673.6:c.4863G= ENSP00000399232.2:p.Gln1621=
ENST00000497886.5:n.2895G=
ENST00000568454.5:c.5004G= ENSP00000454487.1:p.Gln1668=
ENST00000569110.1:c.1354G=
ENST00000569930.1:n.2287G=
NM_000548.3:c.5172G= , LRG_487t1:c.5172G= NP_000539.2:p.Gln1724=
NM_001077183.1:c.4971G= NP_001070651.1:p.Gln1657=
NM_001114382.1:c.5103G= NP_001107854.1:p.Gln1701=
XM_005255529.3:c.5043G= XP_005255586.2:p.Gln1681=
XM_005255531.3:c.4974G= XP_005255588.2:p.Gln1658=
XM_011522636.1:c.5226G= XP_011520938.1:p.Gln1742=
XM_011522637.1:c.5223G= XP_011520939.1:p.Gln1741=
XM_011522638.1:c.5115G= XP_011520940.1:p.Gln1705=
XM_011522639.1:c.5097G= XP_011520941.1:p.Gln1699=
XM_011522640.1:c.5094G= XP_011520942.1:p.Gln1698=
XM_011522641.1:c.4863G= XP_011520943.1:p.Gln1621=
NM_000548.4:c.5172G= NP_000539.2:p.Gln1724=
NM_001077183.2:c.4971G= NP_001070651.1:p.Gln1657=
NM_001114382.2:c.5103G= NP_001107854.1:p.Gln1701=
NM_001318827.1:c.4863G= NP_001305756.1:p.Gln1621=
NM_001318829.1:c.4827G= NP_001305758.1:p.Gln1609=
NM_001318831.1:c.4440G= NP_001305760.1:p.Gln1480=
NM_001318832.1:c.5004G= NP_001305761.1:p.Gln1668=
NM_001363528.1:c.4974G= NP_001350457.1:p.Gln1658=
NM_021055.2:c.5043G= NP_066399.2:p.Gln1681=
XM_005255531.4:c.4974G= XP_005255588.2:p.Gln1658=
XM_011522636.2:c.5226G= XP_011520938.1:p.Gln1742=
XM_011522637.2:c.5223G= XP_011520939.1:p.Gln1741=
XM_011522638.2:c.5388G= XP_011520940.2:p.Gln1796=
XM_011522639.2:c.5097G= XP_011520941.1:p.Gln1699=
XM_011522640.2:c.5094G= XP_011520942.1:p.Gln1698=
XM_017023615.1:c.5169G= XP_016879104.1:p.Gln1723=
XM_017023616.1:c.5040G= XP_016879105.1:p.Gln1680=
XM_017023617.1:c.5136G= XP_016879106.1:p.Gln1712=
XM_017023618.1:c.3882G= XP_016879107.1:p.Gln1294=
XM_024450413.1:c.5058G= XP_024306181.1:p.Gln1686=
NM_000548.5:c.5172G= MANE Select NP_000539.2:p.Gln1724=
NM_001370404.1:c.5040G= NP_001357333.1:p.Gln1680=
NM_001370405.1:c.5032-1G= NP_001357334.1:n.5032-1G=
NM_001077183.3:c.4971G= NP_001070651.1:p.Gln1657=
NM_001114382.3:c.5103G= NP_001107854.1:p.Gln1701=
NM_001318827.2:c.4863G= NP_001305756.1:p.Gln1621=
NM_001318829.2:c.4827G= NP_001305758.1:p.Gln1609=
NM_001318831.2:c.4440G= NP_001305760.1:p.Gln1480=
NM_001318832.2:c.5004G= NP_001305761.1:p.Gln1668=
NM_001363528.2:c.4974G= NP_001350457.1:p.Gln1658=
NM_021055.3:c.5043G= NP_066399.2:p.Gln1681=