Canonical Allele Identifier: CA394314449
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088284T>G , CM000678.2:g.2088284T>G GRCh38
NC_000016.9:g.2138285T>G , CM000678.1:g.2138285T>G GRCh37
NC_000016.8:g.2078286T>G NCBI36
NG_005895.1:g.43979T>G , LRG_487:g.43979T>G
NG_008617.1:g.54937A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3567T>G ENSP00000455997.2:n.*3567T>G
ENST00000642206.2:c.5065T>G ENSP00000495146.2:p.Trp1689Gly
ENST00000642365.2:c.5215T>G ENSP00000495459.2:p.Trp1739Gly
ENST00000644417.2:c.*5731T>G ENSP00000493912.2:n.*5731T>G
ENST00000646464.2:c.*7967T>G ENSP00000496610.2:n.*7967T>G
ENST00000219476.9:c.5218T>G MANE Select ENSP00000219476.3:p.Trp1740Gly
ENST00000350773.9:c.5149T>G ENSP00000344383.4:p.Trp1717Gly
ENST00000401874.7:c.5017T>G ENSP00000384468.2:p.Trp1673Gly
ENST00000568454.6:c.5050T>G ENSP00000454487.1:p.Trp1684Gly
ENST00000569110.2:c.1441T>G
ENST00000569930.2:n.3100T>G
ENST00000642365.1:c.3872T>G
ENST00000642561.1:c.5077T>G ENSP00000495099.1:p.Trp1693Gly
ENST00000642791.1:n.815T>G
ENST00000642797.1:c.5020T>G ENSP00000493846.1:p.Trp1674Gly
ENST00000642936.1:c.5086T>G ENSP00000494514.1:p.Trp1696Gly
ENST00000643088.1:c.5011T>G ENSP00000494747.1:p.Trp1671Gly
ENST00000643426.1:n.2866T>G
ENST00000643946.1:c.5143T>G ENSP00000495927.1:p.Trp1715Gly
ENST00000644043.1:c.5089T>G ENSP00000496262.1:p.Trp1697Gly
ENST00000644329.1:c.5104T>G ENSP00000496611.1:p.Trp1702Gly
ENST00000644335.1:c.5014T>G ENSP00000496317.1:p.Trp1672Gly
ENST00000644399.1:c.5139T>G
ENST00000645024.1:n.3302T>G
ENST00000646388.1:c.5212T>G ENSP00000495921.1:p.Trp1738Gly
ENST00000646634.1:n.4033T>G
ENST00000646674.1:n.2470T>G
ENST00000647042.1:n.2441T>G
ENST00000647180.1:n.2331T>G
ENST00000219476.7:c.5218T>G ENSP00000219476.3:p.Trp1740Gly
ENST00000350773.8:c.5149T>G ENSP00000344383.4:p.Trp1717Gly
ENST00000382538.10:c.4873T>G ENSP00000371978.6:p.Trp1625Gly
ENST00000401874.6:c.5017T>G ENSP00000384468.2:p.Trp1673Gly
ENST00000439117.6:c.*4385T>G ENSP00000406980.2:n.*4385T>G
ENST00000439673.6:c.4909T>G ENSP00000399232.2:p.Trp1637Gly
ENST00000497886.5:n.2941T>G
ENST00000568454.5:c.5050T>G ENSP00000454487.1:p.Trp1684Gly
ENST00000569110.1:c.1400T>G
ENST00000569930.1:n.2333T>G
NM_000548.3:c.5218T>G , LRG_487t1:c.5218T>G NP_000539.2:p.Trp1740Gly
NM_001077183.1:c.5017T>G NP_001070651.1:p.Trp1673Gly
NM_001114382.1:c.5149T>G NP_001107854.1:p.Trp1717Gly
XM_005255529.3:c.5089T>G XP_005255586.2:p.Trp1697Gly
XM_005255531.3:c.5020T>G XP_005255588.2:p.Trp1674Gly
XM_011522636.1:c.5272T>G XP_011520938.1:p.Trp1758Gly
XM_011522637.1:c.5269T>G XP_011520939.1:p.Trp1757Gly
XM_011522638.1:c.5161T>G XP_011520940.1:p.Trp1721Gly
XM_011522639.1:c.5143T>G XP_011520941.1:p.Trp1715Gly
XM_011522640.1:c.5140T>G XP_011520942.1:p.Trp1714Gly
XM_011522641.1:c.4909T>G XP_011520943.1:p.Trp1637Gly
NM_000548.4:c.5218T>G NP_000539.2:p.Trp1740Gly
NM_001077183.2:c.5017T>G NP_001070651.1:p.Trp1673Gly
NM_001114382.2:c.5149T>G NP_001107854.1:p.Trp1717Gly
NM_001318827.1:c.4909T>G NP_001305756.1:p.Trp1637Gly
NM_001318829.1:c.4873T>G NP_001305758.1:p.Trp1625Gly
NM_001318831.1:c.4486T>G NP_001305760.1:p.Trp1496Gly
NM_001318832.1:c.5050T>G NP_001305761.1:p.Trp1684Gly
NM_001363528.1:c.5020T>G NP_001350457.1:p.Trp1674Gly
NM_021055.2:c.5089T>G NP_066399.2:p.Trp1697Gly
XM_005255531.4:c.5020T>G XP_005255588.2:p.Trp1674Gly
XM_011522636.2:c.5272T>G XP_011520938.1:p.Trp1758Gly
XM_011522637.2:c.5269T>G XP_011520939.1:p.Trp1757Gly
XM_011522638.2:c.5434T>G XP_011520940.2:p.Trp1812Gly
XM_011522639.2:c.5143T>G XP_011520941.1:p.Trp1715Gly
XM_011522640.2:c.5140T>G XP_011520942.1:p.Trp1714Gly
XM_017023615.1:c.5215T>G XP_016879104.1:p.Trp1739Gly
XM_017023616.1:c.5086T>G XP_016879105.1:p.Trp1696Gly
XM_017023617.1:c.5182T>G XP_016879106.1:p.Trp1728Gly
XM_017023618.1:c.3928T>G XP_016879107.1:p.Trp1310Gly
XM_024450413.1:c.5104T>G XP_024306181.1:p.Trp1702Gly
NM_000548.5:c.5218T>G MANE Select NP_000539.2:p.Trp1740Gly
NM_001370404.1:c.5086T>G NP_001357333.1:p.Trp1696Gly
NM_001370405.1:c.5077T>G NP_001357334.1:p.Trp1693Gly
NM_001077183.3:c.5017T>G NP_001070651.1:p.Trp1673Gly
NM_001114382.3:c.5149T>G NP_001107854.1:p.Trp1717Gly
NM_001318827.2:c.4909T>G NP_001305756.1:p.Trp1637Gly
NM_001318829.2:c.4873T>G NP_001305758.1:p.Trp1625Gly
NM_001318831.2:c.4486T>G NP_001305760.1:p.Trp1496Gly
NM_001318832.2:c.5050T>G NP_001305761.1:p.Trp1684Gly
NM_001363528.2:c.5020T>G NP_001350457.1:p.Trp1674Gly
NM_021055.3:c.5089T>G NP_066399.2:p.Trp1697Gly