Canonical Allele Identifier: CA2575877453
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088263_2088265del , CM000678.2:g.2088263_2088265del GRCh38
NC_000016.9:g.2138264_2138266del , CM000678.1:g.2138264_2138266del GRCh37
NC_000016.8:g.2078265_2078267del NCBI36
NG_005895.1:g.43958_43960del , LRG_487:g.43958_43960del
NG_008617.1:g.54958_54960del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3546_*3548del ENSP00000455997.2:n.*3546_*3548del
ENST00000642206.2:c.5044_5046del ENSP00000495146.2:p.Thr1682del
ENST00000642365.2:c.5194_5196del ENSP00000495459.2:p.Thr1732del
ENST00000644417.2:c.*5710_*5712del ENSP00000493912.2:n.*5710_*5712del
ENST00000646464.2:c.*7946_*7948del ENSP00000496610.2:n.*7946_*7948del
ENST00000219476.9:c.5197_5199del MANE Select ENSP00000219476.3:p.Thr1733del
ENST00000350773.9:c.5128_5130del ENSP00000344383.4:p.Thr1710del
ENST00000401874.7:c.4996_4998del ENSP00000384468.2:p.Thr1666del
ENST00000568454.6:c.5029_5031del ENSP00000454487.1:p.Thr1677del
ENST00000569110.2:c.1420_1422del
ENST00000569930.2:n.3079_3081del
ENST00000642365.1:c.3851_3853del
ENST00000642561.1:c.5056_5058del ENSP00000495099.1:p.Thr1686del
ENST00000642791.1:n.794_796del
ENST00000642797.1:c.4999_5001del ENSP00000493846.1:p.Thr1667del
ENST00000642936.1:c.5065_5067del ENSP00000494514.1:p.Thr1689del
ENST00000643088.1:c.4990_4992del ENSP00000494747.1:p.Thr1664del
ENST00000643426.1:n.2845_2847del
ENST00000643946.1:c.5122_5124del ENSP00000495927.1:p.Thr1708del
ENST00000644043.1:c.5068_5070del ENSP00000496262.1:p.Thr1690del
ENST00000644329.1:c.5083_5085del ENSP00000496611.1:p.Thr1695del
ENST00000644335.1:c.4993_4995del ENSP00000496317.1:p.Thr1665del
ENST00000644399.1:c.5118_5120del
ENST00000645024.1:n.3281_3283del
ENST00000646388.1:c.5191_5193del ENSP00000495921.1:p.Thr1731del
ENST00000646634.1:n.4012_4014del
ENST00000646674.1:n.2449_2451del
ENST00000647042.1:n.2420_2422del
ENST00000647180.1:n.2310_2312del
ENST00000219476.7:c.5197_5199del ENSP00000219476.3:p.Thr1733del
ENST00000350773.8:c.5128_5130del ENSP00000344383.4:p.Thr1710del
ENST00000382538.10:c.4852_4854del ENSP00000371978.6:p.Thr1618del
ENST00000401874.6:c.4996_4998del ENSP00000384468.2:p.Thr1666del
ENST00000439117.6:c.*4364_*4366del ENSP00000406980.2:n.*4364_*4366del
ENST00000439673.6:c.4888_4890del ENSP00000399232.2:p.Thr1630del
ENST00000497886.5:n.2920_2922del
ENST00000568454.5:c.5029_5031del ENSP00000454487.1:p.Thr1677del
ENST00000569110.1:c.1379_1381del
ENST00000569930.1:n.2312_2314del
NM_000548.3:c.5197_5199del , LRG_487t1:c.5197_5199del NP_000539.2:p.Thr1733del
NM_001077183.1:c.4996_4998del NP_001070651.1:p.Thr1666del
NM_001114382.1:c.5128_5130del NP_001107854.1:p.Thr1710del
XM_005255529.3:c.5068_5070del XP_005255586.2:p.Thr1690del
XM_005255531.3:c.4999_5001del XP_005255588.2:p.Thr1667del
XM_011522636.1:c.5251_5253del XP_011520938.1:p.Thr1751del
XM_011522637.1:c.5248_5250del XP_011520939.1:p.Thr1750del
XM_011522638.1:c.5140_5142del XP_011520940.1:p.Thr1714del
XM_011522639.1:c.5122_5124del XP_011520941.1:p.Thr1708del
XM_011522640.1:c.5119_5121del XP_011520942.1:p.Thr1707del
XM_011522641.1:c.4888_4890del XP_011520943.1:p.Thr1630del
NM_000548.4:c.5197_5199del NP_000539.2:p.Thr1733del
NM_001077183.2:c.4996_4998del NP_001070651.1:p.Thr1666del
NM_001114382.2:c.5128_5130del NP_001107854.1:p.Thr1710del
NM_001318827.1:c.4888_4890del NP_001305756.1:p.Thr1630del
NM_001318829.1:c.4852_4854del NP_001305758.1:p.Thr1618del
NM_001318831.1:c.4465_4467del NP_001305760.1:p.Thr1489del
NM_001318832.1:c.5029_5031del NP_001305761.1:p.Thr1677del
NM_001363528.1:c.4999_5001del NP_001350457.1:p.Thr1667del
NM_021055.2:c.5068_5070del NP_066399.2:p.Thr1690del
XM_005255531.4:c.4999_5001del XP_005255588.2:p.Thr1667del
XM_011522636.2:c.5251_5253del XP_011520938.1:p.Thr1751del
XM_011522637.2:c.5248_5250del XP_011520939.1:p.Thr1750del
XM_011522638.2:c.5413_5415del XP_011520940.2:p.Thr1805del
XM_011522639.2:c.5122_5124del XP_011520941.1:p.Thr1708del
XM_011522640.2:c.5119_5121del XP_011520942.1:p.Thr1707del
XM_017023615.1:c.5194_5196del XP_016879104.1:p.Thr1732del
XM_017023616.1:c.5065_5067del XP_016879105.1:p.Thr1689del
XM_017023617.1:c.5161_5163del XP_016879106.1:p.Thr1721del
XM_017023618.1:c.3907_3909del XP_016879107.1:p.Thr1303del
XM_024450413.1:c.5083_5085del XP_024306181.1:p.Thr1695del
NM_000548.5:c.5197_5199del MANE Select NP_000539.2:p.Thr1733del
NM_001370404.1:c.5065_5067del NP_001357333.1:p.Thr1689del
NM_001370405.1:c.5056_5058del NP_001357334.1:p.Thr1686del
NM_001077183.3:c.4996_4998del NP_001070651.1:p.Thr1666del
NM_001114382.3:c.5128_5130del NP_001107854.1:p.Thr1710del
NM_001318827.2:c.4888_4890del NP_001305756.1:p.Thr1630del
NM_001318829.2:c.4852_4854del NP_001305758.1:p.Thr1618del
NM_001318831.2:c.4465_4467del NP_001305760.1:p.Thr1489del
NM_001318832.2:c.5029_5031del NP_001305761.1:p.Thr1677del
NM_001363528.2:c.4999_5001del NP_001350457.1:p.Thr1667del
NM_021055.3:c.5068_5070del NP_066399.2:p.Thr1690del