Canonical Allele Identifier: CA2202019256
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085261_2085264delinsTCGA , CM000678.2:g.2085261_2085264delinsTCGA GRCh38
NC_000016.9:g.2135262_2135265delinsTCGA , CM000678.1:g.2135262_2135265delinsTCGA GRCh37
NC_000016.8:g.2075263_2075266delinsTCGA NCBI36
NG_005895.1:g.40956_40959delinsTCGA , LRG_487:g.40956_40959delinsTCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2950_*2953delinsTCGA ENSP00000455997.2:n.*2950_*2953delinsTCGA
ENST00000642206.2:c.4448_4451delinsTCGA ENSP00000495146.2:p.Leu1483=
ENST00000642365.2:c.4598_4601delinsTCGA ENSP00000495459.2:p.Leu1533=
ENST00000644417.2:c.*4981_*4984delinsTCGA ENSP00000493912.2:n.*4981_*4984delinsTCGA
ENST00000646464.2:c.*7350_*7353delinsTCGA ENSP00000496610.2:n.*7350_*7353delinsTCGA
ENST00000219476.9:c.4601_4604delinsTCGA MANE Select ENSP00000219476.3:p.Leu1534=
ENST00000350773.9:c.4532_4535delinsTCGA ENSP00000344383.4:p.Leu1511=
ENST00000401874.7:c.4400_4403delinsTCGA ENSP00000384468.2:p.Leu1467=
ENST00000568454.6:c.4433_4436delinsTCGA ENSP00000454487.1:p.Leu1478=
ENST00000569110.2:c.824_827delinsTCGA
ENST00000569930.2:n.2483_2486delinsTCGA
ENST00000642365.1:c.3255_3258delinsTCGA
ENST00000642561.1:c.4472_4475delinsTCGA ENSP00000495099.1:p.Leu1491=
ENST00000642728.1:n.783_786delinsTCGA
ENST00000642791.1:n.198_201delinsTCGA
ENST00000642797.1:c.4403_4406delinsTCGA ENSP00000493846.1:p.Leu1468=
ENST00000642936.1:c.4469_4472delinsTCGA ENSP00000494514.1:p.Leu1490=
ENST00000643088.1:c.4394_4397delinsTCGA ENSP00000494747.1:p.Leu1465=
ENST00000643177.1:n.615_618delinsTCGA
ENST00000643426.1:n.2249_2252delinsTCGA
ENST00000643946.1:c.4526_4529delinsTCGA ENSP00000495927.1:p.Leu1509=
ENST00000644043.1:c.4472_4475delinsTCGA ENSP00000496262.1:p.Leu1491=
ENST00000644278.1:n.83_86delinsTCGA
ENST00000644329.1:c.4400_4403delinsTCGA ENSP00000496611.1:p.Leu1467=
ENST00000644335.1:c.4397_4400delinsTCGA ENSP00000496317.1:p.Leu1466=
ENST00000644399.1:c.4522_4525delinsTCGA
ENST00000645024.1:n.2685_2688delinsTCGA
ENST00000646388.1:c.4595_4598delinsTCGA ENSP00000495921.1:p.Leu1532=
ENST00000646634.1:n.3416_3419delinsTCGA
ENST00000646674.1:n.1853_1856delinsTCGA
ENST00000647042.1:n.1824_1827delinsTCGA
ENST00000647180.1:n.1714_1717delinsTCGA
ENST00000219476.7:c.4601_4604delinsTCGA ENSP00000219476.3:p.Leu1534=
ENST00000350773.8:c.4532_4535delinsTCGA ENSP00000344383.4:p.Leu1511=
ENST00000382538.10:c.4256_4259delinsTCGA ENSP00000371978.6:p.Leu1419=
ENST00000401874.6:c.4400_4403delinsTCGA ENSP00000384468.2:p.Leu1467=
ENST00000439117.6:c.*3768_*3771delinsTCGA ENSP00000406980.2:n.*3768_*3771delinsTCGA
ENST00000439673.6:c.4292_4295delinsTCGA ENSP00000399232.2:p.Leu1431=
ENST00000497886.5:n.2359_2362delinsTCGA
ENST00000568454.5:c.4433_4436delinsTCGA ENSP00000454487.1:p.Leu1478=
ENST00000569110.1:c.783_786delinsTCGA
ENST00000569930.1:n.1716_1719delinsTCGA
NM_000548.3:c.4601_4604delinsTCGA , LRG_487t1:c.4601_4604delinsTCGA NP_000539.2:p.Leu1534=
NM_001077183.1:c.4400_4403delinsTCGA NP_001070651.1:p.Leu1467=
NM_001114382.1:c.4532_4535delinsTCGA NP_001107854.1:p.Leu1511=
XM_005255529.3:c.4472_4475delinsTCGA XP_005255586.2:p.Leu1491=
XM_005255531.3:c.4403_4406delinsTCGA XP_005255588.2:p.Leu1468=
XM_011522636.1:c.4655_4658delinsTCGA XP_011520938.1:p.Leu1552=
XM_011522637.1:c.4652_4655delinsTCGA XP_011520939.1:p.Leu1551=
XM_011522638.1:c.4544_4547delinsTCGA XP_011520940.1:p.Leu1515=
XM_011522639.1:c.4526_4529delinsTCGA XP_011520941.1:p.Leu1509=
XM_011522640.1:c.4523_4526delinsTCGA XP_011520942.1:p.Leu1508=
XM_011522641.1:c.4292_4295delinsTCGA XP_011520943.1:p.Leu1431=
NM_000548.4:c.4601_4604delinsTCGA NP_000539.2:p.Leu1534=
NM_001077183.2:c.4400_4403delinsTCGA NP_001070651.1:p.Leu1467=
NM_001114382.2:c.4532_4535delinsTCGA NP_001107854.1:p.Leu1511=
NM_001318827.1:c.4292_4295delinsTCGA NP_001305756.1:p.Leu1431=
NM_001318829.1:c.4256_4259delinsTCGA NP_001305758.1:p.Leu1419=
NM_001318831.1:c.3869_3872delinsTCGA NP_001305760.1:p.Leu1290=
NM_001318832.1:c.4433_4436delinsTCGA NP_001305761.1:p.Leu1478=
NM_001363528.1:c.4403_4406delinsTCGA NP_001350457.1:p.Leu1468=
NM_021055.2:c.4472_4475delinsTCGA NP_066399.2:p.Leu1491=
XM_005255531.4:c.4403_4406delinsTCGA XP_005255588.2:p.Leu1468=
XM_011522636.2:c.4655_4658delinsTCGA XP_011520938.1:p.Leu1552=
XM_011522637.2:c.4652_4655delinsTCGA XP_011520939.1:p.Leu1551=
XM_011522638.2:c.4817_4820delinsTCGA XP_011520940.2:p.Leu1606=
XM_011522639.2:c.4526_4529delinsTCGA XP_011520941.1:p.Leu1509=
XM_011522640.2:c.4523_4526delinsTCGA XP_011520942.1:p.Leu1508=
XM_017023615.1:c.4598_4601delinsTCGA XP_016879104.1:p.Leu1533=
XM_017023616.1:c.4469_4472delinsTCGA XP_016879105.1:p.Leu1490=
XM_017023617.1:c.4565_4568delinsTCGA XP_016879106.1:p.Leu1522=
XM_017023618.1:c.3311_3314delinsTCGA XP_016879107.1:p.Leu1104=
XM_024450413.1:c.4400_4403delinsTCGA XP_024306181.1:p.Leu1467=
NM_000548.5:c.4601_4604delinsTCGA MANE Select NP_000539.2:p.Leu1534=
NM_001370404.1:c.4469_4472delinsTCGA NP_001357333.1:p.Leu1490=
NM_001370405.1:c.4472_4475delinsTCGA NP_001357334.1:p.Leu1491=
NM_001077183.3:c.4400_4403delinsTCGA NP_001070651.1:p.Leu1467=
NM_001114382.3:c.4532_4535delinsTCGA NP_001107854.1:p.Leu1511=
NM_001318827.2:c.4292_4295delinsTCGA NP_001305756.1:p.Leu1431=
NM_001318829.2:c.4256_4259delinsTCGA NP_001305758.1:p.Leu1419=
NM_001318831.2:c.3869_3872delinsTCGA NP_001305760.1:p.Leu1290=
NM_001318832.2:c.4433_4436delinsTCGA NP_001305761.1:p.Leu1478=
NM_001363528.2:c.4403_4406delinsTCGA NP_001350457.1:p.Leu1468=
NM_021055.3:c.4472_4475delinsTCGA NP_066399.2:p.Leu1491=