Canonical Allele Identifier: CA394314149
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959546
dbSNP Id: rs2091134565
gnomAD v4: 16-2088255-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088255C>G , CM000678.2:g.2088255C>G GRCh38
NC_000016.9:g.2138256C>G , CM000678.1:g.2138256C>G GRCh37
NC_000016.8:g.2078257C>G NCBI36
NG_005895.1:g.43950C>G , LRG_487:g.43950C>G
NG_008617.1:g.54966G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3538C>G ENSP00000455997.2:n.*3538C>G
ENST00000642206.2:c.5036C>G ENSP00000495146.2:p.Ser1679Cys
ENST00000642365.2:c.5186C>G ENSP00000495459.2:p.Ser1729Cys
ENST00000644417.2:c.*5702C>G ENSP00000493912.2:n.*5702C>G
ENST00000646464.2:c.*7938C>G ENSP00000496610.2:n.*7938C>G
ENST00000219476.9:c.5189C>G MANE Select ENSP00000219476.3:p.Ser1730Cys
ENST00000350773.9:c.5120C>G ENSP00000344383.4:p.Ser1707Cys
ENST00000401874.7:c.4988C>G ENSP00000384468.2:p.Ser1663Cys
ENST00000568454.6:c.5021C>G ENSP00000454487.1:p.Ser1674Cys
ENST00000569110.2:c.1412C>G
ENST00000569930.2:n.3071C>G
ENST00000642365.1:c.3843C>G
ENST00000642561.1:c.5048C>G ENSP00000495099.1:p.Ser1683Cys
ENST00000642791.1:n.786C>G
ENST00000642797.1:c.4991C>G ENSP00000493846.1:p.Ser1664Cys
ENST00000642936.1:c.5057C>G ENSP00000494514.1:p.Ser1686Cys
ENST00000643088.1:c.4982C>G ENSP00000494747.1:p.Ser1661Cys
ENST00000643426.1:n.2837C>G
ENST00000643946.1:c.5114C>G ENSP00000495927.1:p.Ser1705Cys
ENST00000644043.1:c.5060C>G ENSP00000496262.1:p.Ser1687Cys
ENST00000644329.1:c.5075C>G ENSP00000496611.1:p.Ser1692Cys
ENST00000644335.1:c.4985C>G ENSP00000496317.1:p.Ser1662Cys
ENST00000644399.1:c.5110C>G
ENST00000645024.1:n.3273C>G
ENST00000646388.1:c.5183C>G ENSP00000495921.1:p.Ser1728Cys
ENST00000646634.1:n.4004C>G
ENST00000646674.1:n.2441C>G
ENST00000647042.1:n.2412C>G
ENST00000647180.1:n.2302C>G
ENST00000219476.7:c.5189C>G ENSP00000219476.3:p.Ser1730Cys
ENST00000350773.8:c.5120C>G ENSP00000344383.4:p.Ser1707Cys
ENST00000382538.10:c.4844C>G ENSP00000371978.6:p.Ser1615Cys
ENST00000401874.6:c.4988C>G ENSP00000384468.2:p.Ser1663Cys
ENST00000439117.6:c.*4356C>G ENSP00000406980.2:n.*4356C>G
ENST00000439673.6:c.4880C>G ENSP00000399232.2:p.Ser1627Cys
ENST00000497886.5:n.2912C>G
ENST00000568454.5:c.5021C>G ENSP00000454487.1:p.Ser1674Cys
ENST00000569110.1:c.1371C>G
ENST00000569930.1:n.2304C>G
NM_000548.3:c.5189C>G , LRG_487t1:c.5189C>G NP_000539.2:p.Ser1730Cys
NM_001077183.1:c.4988C>G NP_001070651.1:p.Ser1663Cys
NM_001114382.1:c.5120C>G NP_001107854.1:p.Ser1707Cys
XM_005255529.3:c.5060C>G XP_005255586.2:p.Ser1687Cys
XM_005255531.3:c.4991C>G XP_005255588.2:p.Ser1664Cys
XM_011522636.1:c.5243C>G XP_011520938.1:p.Ser1748Cys
XM_011522637.1:c.5240C>G XP_011520939.1:p.Ser1747Cys
XM_011522638.1:c.5132C>G XP_011520940.1:p.Ser1711Cys
XM_011522639.1:c.5114C>G XP_011520941.1:p.Ser1705Cys
XM_011522640.1:c.5111C>G XP_011520942.1:p.Ser1704Cys
XM_011522641.1:c.4880C>G XP_011520943.1:p.Ser1627Cys
NM_000548.4:c.5189C>G NP_000539.2:p.Ser1730Cys
NM_001077183.2:c.4988C>G NP_001070651.1:p.Ser1663Cys
NM_001114382.2:c.5120C>G NP_001107854.1:p.Ser1707Cys
NM_001318827.1:c.4880C>G NP_001305756.1:p.Ser1627Cys
NM_001318829.1:c.4844C>G NP_001305758.1:p.Ser1615Cys
NM_001318831.1:c.4457C>G NP_001305760.1:p.Ser1486Cys
NM_001318832.1:c.5021C>G NP_001305761.1:p.Ser1674Cys
NM_001363528.1:c.4991C>G NP_001350457.1:p.Ser1664Cys
NM_021055.2:c.5060C>G NP_066399.2:p.Ser1687Cys
XM_005255531.4:c.4991C>G XP_005255588.2:p.Ser1664Cys
XM_011522636.2:c.5243C>G XP_011520938.1:p.Ser1748Cys
XM_011522637.2:c.5240C>G XP_011520939.1:p.Ser1747Cys
XM_011522638.2:c.5405C>G XP_011520940.2:p.Ser1802Cys
XM_011522639.2:c.5114C>G XP_011520941.1:p.Ser1705Cys
XM_011522640.2:c.5111C>G XP_011520942.1:p.Ser1704Cys
XM_017023615.1:c.5186C>G XP_016879104.1:p.Ser1729Cys
XM_017023616.1:c.5057C>G XP_016879105.1:p.Ser1686Cys
XM_017023617.1:c.5153C>G XP_016879106.1:p.Ser1718Cys
XM_017023618.1:c.3899C>G XP_016879107.1:p.Ser1300Cys
XM_024450413.1:c.5075C>G XP_024306181.1:p.Ser1692Cys
NM_000548.5:c.5189C>G MANE Select NP_000539.2:p.Ser1730Cys
NM_001370404.1:c.5057C>G NP_001357333.1:p.Ser1686Cys
NM_001370405.1:c.5048C>G NP_001357334.1:p.Ser1683Cys
NM_001077183.3:c.4988C>G NP_001070651.1:p.Ser1663Cys
NM_001114382.3:c.5120C>G NP_001107854.1:p.Ser1707Cys
NM_001318827.2:c.4880C>G NP_001305756.1:p.Ser1627Cys
NM_001318829.2:c.4844C>G NP_001305758.1:p.Ser1615Cys
NM_001318831.2:c.4457C>G NP_001305760.1:p.Ser1486Cys
NM_001318832.2:c.5021C>G NP_001305761.1:p.Ser1674Cys
NM_001363528.2:c.4991C>G NP_001350457.1:p.Ser1664Cys
NM_021055.3:c.5060C>G NP_066399.2:p.Ser1687Cys