Canonical Allele Identifier: CA2202034140
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088543C= , CM000678.2:g.2088543C= GRCh38
NC_000016.9:g.2138544C= , CM000678.1:g.2138544C= GRCh37
NC_000016.8:g.2078545C= NCBI36
NG_005895.1:g.44238C= , LRG_487:g.44238C=
NG_008617.1:g.54678G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3706C= ENSP00000455997.2:n.*3706C=
ENST00000642206.2:c.5204C= ENSP00000495146.2:p.Pro1735=
ENST00000642365.2:c.5354C= ENSP00000495459.2:p.Pro1785=
ENST00000644417.2:c.*5870C= ENSP00000493912.2:n.*5870C=
ENST00000646464.2:c.*8106C= ENSP00000496610.2:n.*8106C=
ENST00000219476.9:c.5357C= MANE Select ENSP00000219476.3:p.Pro1786=
ENST00000350773.9:c.5288C= ENSP00000344383.4:p.Pro1763=
ENST00000401874.7:c.5156C= ENSP00000384468.2:p.Pro1719=
ENST00000568454.6:c.5189C= ENSP00000454487.1:p.Pro1730=
ENST00000569110.2:c.1580C=
ENST00000569930.2:n.3239C=
ENST00000642365.1:c.4011C=
ENST00000642561.1:c.5216C= ENSP00000495099.1:p.Pro1739=
ENST00000642791.1:n.954C=
ENST00000642797.1:c.5159C= ENSP00000493846.1:p.Pro1720=
ENST00000642936.1:c.5225C= ENSP00000494514.1:p.Pro1742=
ENST00000643088.1:c.5150C= ENSP00000494747.1:p.Pro1717=
ENST00000643426.1:n.3005C=
ENST00000643946.1:c.5282C= ENSP00000495927.1:p.Pro1761=
ENST00000644043.1:c.5228C= ENSP00000496262.1:p.Pro1743=
ENST00000644329.1:c.5243C= ENSP00000496611.1:p.Pro1748=
ENST00000644335.1:c.5153C= ENSP00000496317.1:p.Pro1718=
ENST00000644399.1:c.5278C=
ENST00000645024.1:n.3441C=
ENST00000646388.1:c.5351C= ENSP00000495921.1:p.Pro1784=
ENST00000646634.1:n.4172C=
ENST00000646674.1:n.2609C=
ENST00000647042.1:n.2580C=
ENST00000647180.1:n.2470C=
ENST00000219476.7:c.5357C= ENSP00000219476.3:p.Pro1786=
ENST00000350773.8:c.5288C= ENSP00000344383.4:p.Pro1763=
ENST00000382538.10:c.5012C= ENSP00000371978.6:p.Pro1671=
ENST00000401874.6:c.5156C= ENSP00000384468.2:p.Pro1719=
ENST00000439117.6:c.*4524C= ENSP00000406980.2:n.*4524C=
ENST00000439673.6:c.5048C= ENSP00000399232.2:p.Pro1683=
ENST00000497886.5:n.3080C=
ENST00000568454.5:c.5189C= ENSP00000454487.1:p.Pro1730=
ENST00000569110.1:c.1539C=
ENST00000569930.1:n.2472C=
NM_000548.3:c.5357C= , LRG_487t1:c.5357C= NP_000539.2:p.Pro1786=
NM_001077183.1:c.5156C= NP_001070651.1:p.Pro1719=
NM_001114382.1:c.5288C= NP_001107854.1:p.Pro1763=
XM_005255529.3:c.5228C= XP_005255586.2:p.Pro1743=
XM_005255531.3:c.5159C= XP_005255588.2:p.Pro1720=
XM_011522636.1:c.5411C= XP_011520938.1:p.Pro1804=
XM_011522637.1:c.5408C= XP_011520939.1:p.Pro1803=
XM_011522638.1:c.5300C= XP_011520940.1:p.Pro1767=
XM_011522639.1:c.5282C= XP_011520941.1:p.Pro1761=
XM_011522640.1:c.5279C= XP_011520942.1:p.Pro1760=
XM_011522641.1:c.5048C= XP_011520943.1:p.Pro1683=
NM_000548.4:c.5357C= NP_000539.2:p.Pro1786=
NM_001077183.2:c.5156C= NP_001070651.1:p.Pro1719=
NM_001114382.2:c.5288C= NP_001107854.1:p.Pro1763=
NM_001318827.1:c.5048C= NP_001305756.1:p.Pro1683=
NM_001318829.1:c.5012C= NP_001305758.1:p.Pro1671=
NM_001318831.1:c.4625C= NP_001305760.1:p.Pro1542=
NM_001318832.1:c.5189C= NP_001305761.1:p.Pro1730=
NM_001363528.1:c.5159C= NP_001350457.1:p.Pro1720=
NM_021055.2:c.5228C= NP_066399.2:p.Pro1743=
XM_005255531.4:c.5159C= XP_005255588.2:p.Pro1720=
XM_011522636.2:c.5411C= XP_011520938.1:p.Pro1804=
XM_011522637.2:c.5408C= XP_011520939.1:p.Pro1803=
XM_011522638.2:c.5573C= XP_011520940.2:p.Pro1858=
XM_011522639.2:c.5282C= XP_011520941.1:p.Pro1761=
XM_011522640.2:c.5279C= XP_011520942.1:p.Pro1760=
XM_017023615.1:c.5354C= XP_016879104.1:p.Pro1785=
XM_017023616.1:c.5225C= XP_016879105.1:p.Pro1742=
XM_017023617.1:c.5321C= XP_016879106.1:p.Pro1774=
XM_017023618.1:c.4067C= XP_016879107.1:p.Pro1356=
XM_024450413.1:c.5243C= XP_024306181.1:p.Pro1748=
NM_000548.5:c.5357C= MANE Select NP_000539.2:p.Pro1786=
NM_001370404.1:c.5225C= NP_001357333.1:p.Pro1742=
NM_001370405.1:c.5216C= NP_001357334.1:p.Pro1739=
NM_001077183.3:c.5156C= NP_001070651.1:p.Pro1719=
NM_001114382.3:c.5288C= NP_001107854.1:p.Pro1763=
NM_001318827.2:c.5048C= NP_001305756.1:p.Pro1683=
NM_001318829.2:c.5012C= NP_001305758.1:p.Pro1671=
NM_001318831.2:c.4625C= NP_001305760.1:p.Pro1542=
NM_001318832.2:c.5189C= NP_001305761.1:p.Pro1730=
NM_001363528.2:c.5159C= NP_001350457.1:p.Pro1720=
NM_021055.3:c.5228C= NP_066399.2:p.Pro1743=