Canonical Allele Identifier: CA394304611
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085261T>G , CM000678.2:g.2085261T>G GRCh38
NC_000016.9:g.2135262T>G , CM000678.1:g.2135262T>G GRCh37
NC_000016.8:g.2075263T>G NCBI36
NG_005895.1:g.40956T>G , LRG_487:g.40956T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2950T>G ENSP00000455997.2:n.*2950T>G
ENST00000642206.2:c.4448T>G ENSP00000495146.2:p.Leu1483Arg
ENST00000642365.2:c.4598T>G ENSP00000495459.2:p.Leu1533Arg
ENST00000644417.2:c.*4981T>G ENSP00000493912.2:n.*4981T>G
ENST00000646464.2:c.*7350T>G ENSP00000496610.2:n.*7350T>G
ENST00000219476.9:c.4601T>G MANE Select ENSP00000219476.3:p.Leu1534Arg
ENST00000350773.9:c.4532T>G ENSP00000344383.4:p.Leu1511Arg
ENST00000401874.7:c.4400T>G ENSP00000384468.2:p.Leu1467Arg
ENST00000568454.6:c.4433T>G ENSP00000454487.1:p.Leu1478Arg
ENST00000569110.2:c.824T>G
ENST00000569930.2:n.2483T>G
ENST00000642365.1:c.3255T>G
ENST00000642561.1:c.4472T>G ENSP00000495099.1:p.Leu1491Arg
ENST00000642728.1:n.783T>G
ENST00000642791.1:n.198T>G
ENST00000642797.1:c.4403T>G ENSP00000493846.1:p.Leu1468Arg
ENST00000642936.1:c.4469T>G ENSP00000494514.1:p.Leu1490Arg
ENST00000643088.1:c.4394T>G ENSP00000494747.1:p.Leu1465Arg
ENST00000643177.1:n.615T>G
ENST00000643426.1:n.2249T>G
ENST00000643946.1:c.4526T>G ENSP00000495927.1:p.Leu1509Arg
ENST00000644043.1:c.4472T>G ENSP00000496262.1:p.Leu1491Arg
ENST00000644278.1:n.83T>G
ENST00000644329.1:c.4400T>G ENSP00000496611.1:p.Leu1467Arg
ENST00000644335.1:c.4397T>G ENSP00000496317.1:p.Leu1466Arg
ENST00000644399.1:c.4522T>G
ENST00000645024.1:n.2685T>G
ENST00000646388.1:c.4595T>G ENSP00000495921.1:p.Leu1532Arg
ENST00000646634.1:n.3416T>G
ENST00000646674.1:n.1853T>G
ENST00000647042.1:n.1824T>G
ENST00000647180.1:n.1714T>G
ENST00000219476.7:c.4601T>G ENSP00000219476.3:p.Leu1534Arg
ENST00000350773.8:c.4532T>G ENSP00000344383.4:p.Leu1511Arg
ENST00000382538.10:c.4256T>G ENSP00000371978.6:p.Leu1419Arg
ENST00000401874.6:c.4400T>G ENSP00000384468.2:p.Leu1467Arg
ENST00000439117.6:c.*3768T>G ENSP00000406980.2:n.*3768T>G
ENST00000439673.6:c.4292T>G ENSP00000399232.2:p.Leu1431Arg
ENST00000497886.5:n.2359T>G
ENST00000568454.5:c.4433T>G ENSP00000454487.1:p.Leu1478Arg
ENST00000569110.1:c.783T>G
ENST00000569930.1:n.1716T>G
NM_000548.3:c.4601T>G , LRG_487t1:c.4601T>G NP_000539.2:p.Leu1534Arg
NM_001077183.1:c.4400T>G NP_001070651.1:p.Leu1467Arg
NM_001114382.1:c.4532T>G NP_001107854.1:p.Leu1511Arg
XM_005255529.3:c.4472T>G XP_005255586.2:p.Leu1491Arg
XM_005255531.3:c.4403T>G XP_005255588.2:p.Leu1468Arg
XM_011522636.1:c.4655T>G XP_011520938.1:p.Leu1552Arg
XM_011522637.1:c.4652T>G XP_011520939.1:p.Leu1551Arg
XM_011522638.1:c.4544T>G XP_011520940.1:p.Leu1515Arg
XM_011522639.1:c.4526T>G XP_011520941.1:p.Leu1509Arg
XM_011522640.1:c.4523T>G XP_011520942.1:p.Leu1508Arg
XM_011522641.1:c.4292T>G XP_011520943.1:p.Leu1431Arg
NM_000548.4:c.4601T>G NP_000539.2:p.Leu1534Arg
NM_001077183.2:c.4400T>G NP_001070651.1:p.Leu1467Arg
NM_001114382.2:c.4532T>G NP_001107854.1:p.Leu1511Arg
NM_001318827.1:c.4292T>G NP_001305756.1:p.Leu1431Arg
NM_001318829.1:c.4256T>G NP_001305758.1:p.Leu1419Arg
NM_001318831.1:c.3869T>G NP_001305760.1:p.Leu1290Arg
NM_001318832.1:c.4433T>G NP_001305761.1:p.Leu1478Arg
NM_001363528.1:c.4403T>G NP_001350457.1:p.Leu1468Arg
NM_021055.2:c.4472T>G NP_066399.2:p.Leu1491Arg
XM_005255531.4:c.4403T>G XP_005255588.2:p.Leu1468Arg
XM_011522636.2:c.4655T>G XP_011520938.1:p.Leu1552Arg
XM_011522637.2:c.4652T>G XP_011520939.1:p.Leu1551Arg
XM_011522638.2:c.4817T>G XP_011520940.2:p.Leu1606Arg
XM_011522639.2:c.4526T>G XP_011520941.1:p.Leu1509Arg
XM_011522640.2:c.4523T>G XP_011520942.1:p.Leu1508Arg
XM_017023615.1:c.4598T>G XP_016879104.1:p.Leu1533Arg
XM_017023616.1:c.4469T>G XP_016879105.1:p.Leu1490Arg
XM_017023617.1:c.4565T>G XP_016879106.1:p.Leu1522Arg
XM_017023618.1:c.3311T>G XP_016879107.1:p.Leu1104Arg
XM_024450413.1:c.4400T>G XP_024306181.1:p.Leu1467Arg
NM_000548.5:c.4601T>G MANE Select NP_000539.2:p.Leu1534Arg
NM_001370404.1:c.4469T>G NP_001357333.1:p.Leu1490Arg
NM_001370405.1:c.4472T>G NP_001357334.1:p.Leu1491Arg
NM_001077183.3:c.4400T>G NP_001070651.1:p.Leu1467Arg
NM_001114382.3:c.4532T>G NP_001107854.1:p.Leu1511Arg
NM_001318827.2:c.4292T>G NP_001305756.1:p.Leu1431Arg
NM_001318829.2:c.4256T>G NP_001305758.1:p.Leu1419Arg
NM_001318831.2:c.3869T>G NP_001305760.1:p.Leu1290Arg
NM_001318832.2:c.4433T>G NP_001305761.1:p.Leu1478Arg
NM_001363528.2:c.4403T>G NP_001350457.1:p.Leu1468Arg
NM_021055.3:c.4472T>G NP_066399.2:p.Leu1491Arg