Canonical Allele Identifier: CA2202019113
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085241T= , CM000678.2:g.2085241T= GRCh38
NC_000016.9:g.2135242T= , CM000678.1:g.2135242T= GRCh37
NC_000016.8:g.2075243T= NCBI36
NG_005895.1:g.40936T= , LRG_487:g.40936T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2930T= ENSP00000455997.2:n.*2930T=
ENST00000642206.2:c.4428T= ENSP00000495146.2:p.Phe1476=
ENST00000642365.2:c.4578T= ENSP00000495459.2:p.Phe1526=
ENST00000644417.2:c.*4961T= ENSP00000493912.2:n.*4961T=
ENST00000646464.2:c.*7330T= ENSP00000496610.2:n.*7330T=
ENST00000219476.9:c.4581T= MANE Select ENSP00000219476.3:p.Phe1527=
ENST00000350773.9:c.4512T= ENSP00000344383.4:p.Phe1504=
ENST00000401874.7:c.4380T= ENSP00000384468.2:p.Phe1460=
ENST00000568454.6:c.4413T= ENSP00000454487.1:p.Phe1471=
ENST00000569110.2:c.804T=
ENST00000569930.2:n.2463T=
ENST00000642365.1:c.3235T=
ENST00000642561.1:c.4452T= ENSP00000495099.1:p.Phe1484=
ENST00000642728.1:n.763T=
ENST00000642791.1:n.178T=
ENST00000642797.1:c.4383T= ENSP00000493846.1:p.Phe1461=
ENST00000642936.1:c.4449T= ENSP00000494514.1:p.Phe1483=
ENST00000643088.1:c.4374T= ENSP00000494747.1:p.Phe1458=
ENST00000643177.1:n.595T=
ENST00000643426.1:n.2229T=
ENST00000643946.1:c.4506T= ENSP00000495927.1:p.Phe1502=
ENST00000644043.1:c.4452T= ENSP00000496262.1:p.Phe1484=
ENST00000644278.1:n.63T=
ENST00000644329.1:c.4380T= ENSP00000496611.1:p.Phe1460=
ENST00000644335.1:c.4377T= ENSP00000496317.1:p.Phe1459=
ENST00000644399.1:c.4502T=
ENST00000645024.1:n.2665T=
ENST00000646388.1:c.4575T= ENSP00000495921.1:p.Phe1525=
ENST00000646634.1:n.3396T=
ENST00000646674.1:n.1833T=
ENST00000647042.1:n.1804T=
ENST00000647180.1:n.1694T=
ENST00000219476.7:c.4581T= ENSP00000219476.3:p.Phe1527=
ENST00000350773.8:c.4512T= ENSP00000344383.4:p.Phe1504=
ENST00000382538.10:c.4236T= ENSP00000371978.6:p.Phe1412=
ENST00000401874.6:c.4380T= ENSP00000384468.2:p.Phe1460=
ENST00000439117.6:c.*3748T= ENSP00000406980.2:n.*3748T=
ENST00000439673.6:c.4272T= ENSP00000399232.2:p.Phe1424=
ENST00000497886.5:n.2339T=
ENST00000568454.5:c.4413T= ENSP00000454487.1:p.Phe1471=
ENST00000569110.1:c.763T=
ENST00000569930.1:n.1696T=
NM_000548.3:c.4581T= , LRG_487t1:c.4581T= NP_000539.2:p.Phe1527=
NM_001077183.1:c.4380T= NP_001070651.1:p.Phe1460=
NM_001114382.1:c.4512T= NP_001107854.1:p.Phe1504=
XM_005255529.3:c.4452T= XP_005255586.2:p.Phe1484=
XM_005255531.3:c.4383T= XP_005255588.2:p.Phe1461=
XM_011522636.1:c.4635T= XP_011520938.1:p.Phe1545=
XM_011522637.1:c.4632T= XP_011520939.1:p.Phe1544=
XM_011522638.1:c.4524T= XP_011520940.1:p.Phe1508=
XM_011522639.1:c.4506T= XP_011520941.1:p.Phe1502=
XM_011522640.1:c.4503T= XP_011520942.1:p.Phe1501=
XM_011522641.1:c.4272T= XP_011520943.1:p.Phe1424=
NM_000548.4:c.4581T= NP_000539.2:p.Phe1527=
NM_001077183.2:c.4380T= NP_001070651.1:p.Phe1460=
NM_001114382.2:c.4512T= NP_001107854.1:p.Phe1504=
NM_001318827.1:c.4272T= NP_001305756.1:p.Phe1424=
NM_001318829.1:c.4236T= NP_001305758.1:p.Phe1412=
NM_001318831.1:c.3849T= NP_001305760.1:p.Phe1283=
NM_001318832.1:c.4413T= NP_001305761.1:p.Phe1471=
NM_001363528.1:c.4383T= NP_001350457.1:p.Phe1461=
NM_021055.2:c.4452T= NP_066399.2:p.Phe1484=
XM_005255531.4:c.4383T= XP_005255588.2:p.Phe1461=
XM_011522636.2:c.4635T= XP_011520938.1:p.Phe1545=
XM_011522637.2:c.4632T= XP_011520939.1:p.Phe1544=
XM_011522638.2:c.4797T= XP_011520940.2:p.Phe1599=
XM_011522639.2:c.4506T= XP_011520941.1:p.Phe1502=
XM_011522640.2:c.4503T= XP_011520942.1:p.Phe1501=
XM_017023615.1:c.4578T= XP_016879104.1:p.Phe1526=
XM_017023616.1:c.4449T= XP_016879105.1:p.Phe1483=
XM_017023617.1:c.4545T= XP_016879106.1:p.Phe1515=
XM_017023618.1:c.3291T= XP_016879107.1:p.Phe1097=
XM_024450413.1:c.4380T= XP_024306181.1:p.Phe1460=
NM_000548.5:c.4581T= MANE Select NP_000539.2:p.Phe1527=
NM_001370404.1:c.4449T= NP_001357333.1:p.Phe1483=
NM_001370405.1:c.4452T= NP_001357334.1:p.Phe1484=
NM_001077183.3:c.4380T= NP_001070651.1:p.Phe1460=
NM_001114382.3:c.4512T= NP_001107854.1:p.Phe1504=
NM_001318827.2:c.4272T= NP_001305756.1:p.Phe1424=
NM_001318829.2:c.4236T= NP_001305758.1:p.Phe1412=
NM_001318831.2:c.3849T= NP_001305760.1:p.Phe1283=
NM_001318832.2:c.4413T= NP_001305761.1:p.Phe1471=
NM_001363528.2:c.4383T= NP_001350457.1:p.Phe1461=
NM_021055.3:c.4452T= NP_066399.2:p.Phe1484=