Canonical Allele Identifier: CA394314708
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1555440785

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088312G>T , CM000678.2:g.2088312G>T GRCh38
NC_000016.9:g.2138313G>T , CM000678.1:g.2138313G>T GRCh37
NC_000016.8:g.2078314G>T NCBI36
NG_005895.1:g.44007G>T , LRG_487:g.44007G>T
NG_008617.1:g.54909C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3595G>T ENSP00000455997.2:n.*3595G>T
ENST00000642206.2:c.5093G>T ENSP00000495146.2:p.Arg1698Leu
ENST00000642365.2:c.5243G>T ENSP00000495459.2:p.Arg1748Leu
ENST00000644417.2:c.*5759G>T ENSP00000493912.2:n.*5759G>T
ENST00000646464.2:c.*7995G>T ENSP00000496610.2:n.*7995G>T
ENST00000219476.9:c.5246G>T MANE Select ENSP00000219476.3:p.Arg1749Leu
ENST00000350773.9:c.5177G>T ENSP00000344383.4:p.Arg1726Leu
ENST00000401874.7:c.5045G>T ENSP00000384468.2:p.Arg1682Leu
ENST00000568454.6:c.5078G>T ENSP00000454487.1:p.Arg1693Leu
ENST00000569110.2:c.1469G>T
ENST00000569930.2:n.3128G>T
ENST00000642365.1:c.3900G>T
ENST00000642561.1:c.5105G>T ENSP00000495099.1:p.Arg1702Leu
ENST00000642791.1:n.843G>T
ENST00000642797.1:c.5048G>T ENSP00000493846.1:p.Arg1683Leu
ENST00000642936.1:c.5114G>T ENSP00000494514.1:p.Arg1705Leu
ENST00000643088.1:c.5039G>T ENSP00000494747.1:p.Arg1680Leu
ENST00000643426.1:n.2894G>T
ENST00000643946.1:c.5171G>T ENSP00000495927.1:p.Arg1724Leu
ENST00000644043.1:c.5117G>T ENSP00000496262.1:p.Arg1706Leu
ENST00000644329.1:c.5132G>T ENSP00000496611.1:p.Arg1711Leu
ENST00000644335.1:c.5042G>T ENSP00000496317.1:p.Arg1681Leu
ENST00000644399.1:c.5167G>T
ENST00000645024.1:n.3330G>T
ENST00000646388.1:c.5240G>T ENSP00000495921.1:p.Arg1747Leu
ENST00000646634.1:n.4061G>T
ENST00000646674.1:n.2498G>T
ENST00000647042.1:n.2469G>T
ENST00000647180.1:n.2359G>T
ENST00000219476.7:c.5246G>T ENSP00000219476.3:p.Arg1749Leu
ENST00000350773.8:c.5177G>T ENSP00000344383.4:p.Arg1726Leu
ENST00000382538.10:c.4901G>T ENSP00000371978.6:p.Arg1634Leu
ENST00000401874.6:c.5045G>T ENSP00000384468.2:p.Arg1682Leu
ENST00000439117.6:c.*4413G>T ENSP00000406980.2:n.*4413G>T
ENST00000439673.6:c.4937G>T ENSP00000399232.2:p.Arg1646Leu
ENST00000497886.5:n.2969G>T
ENST00000568454.5:c.5078G>T ENSP00000454487.1:p.Arg1693Leu
ENST00000569110.1:c.1428G>T
ENST00000569930.1:n.2361G>T
NM_000548.3:c.5246G>T , LRG_487t1:c.5246G>T NP_000539.2:p.Arg1749Leu
NM_001077183.1:c.5045G>T NP_001070651.1:p.Arg1682Leu
NM_001114382.1:c.5177G>T NP_001107854.1:p.Arg1726Leu
XM_005255529.3:c.5117G>T XP_005255586.2:p.Arg1706Leu
XM_005255531.3:c.5048G>T XP_005255588.2:p.Arg1683Leu
XM_011522636.1:c.5300G>T XP_011520938.1:p.Arg1767Leu
XM_011522637.1:c.5297G>T XP_011520939.1:p.Arg1766Leu
XM_011522638.1:c.5189G>T XP_011520940.1:p.Arg1730Leu
XM_011522639.1:c.5171G>T XP_011520941.1:p.Arg1724Leu
XM_011522640.1:c.5168G>T XP_011520942.1:p.Arg1723Leu
XM_011522641.1:c.4937G>T XP_011520943.1:p.Arg1646Leu
NM_000548.4:c.5246G>T NP_000539.2:p.Arg1749Leu
NM_001077183.2:c.5045G>T NP_001070651.1:p.Arg1682Leu
NM_001114382.2:c.5177G>T NP_001107854.1:p.Arg1726Leu
NM_001318827.1:c.4937G>T NP_001305756.1:p.Arg1646Leu
NM_001318829.1:c.4901G>T NP_001305758.1:p.Arg1634Leu
NM_001318831.1:c.4514G>T NP_001305760.1:p.Arg1505Leu
NM_001318832.1:c.5078G>T NP_001305761.1:p.Arg1693Leu
NM_001363528.1:c.5048G>T NP_001350457.1:p.Arg1683Leu
NM_021055.2:c.5117G>T NP_066399.2:p.Arg1706Leu
XM_005255531.4:c.5048G>T XP_005255588.2:p.Arg1683Leu
XM_011522636.2:c.5300G>T XP_011520938.1:p.Arg1767Leu
XM_011522637.2:c.5297G>T XP_011520939.1:p.Arg1766Leu
XM_011522638.2:c.5462G>T XP_011520940.2:p.Arg1821Leu
XM_011522639.2:c.5171G>T XP_011520941.1:p.Arg1724Leu
XM_011522640.2:c.5168G>T XP_011520942.1:p.Arg1723Leu
XM_017023615.1:c.5243G>T XP_016879104.1:p.Arg1748Leu
XM_017023616.1:c.5114G>T XP_016879105.1:p.Arg1705Leu
XM_017023617.1:c.5210G>T XP_016879106.1:p.Arg1737Leu
XM_017023618.1:c.3956G>T XP_016879107.1:p.Arg1319Leu
XM_024450413.1:c.5132G>T XP_024306181.1:p.Arg1711Leu
NM_000548.5:c.5246G>T MANE Select NP_000539.2:p.Arg1749Leu
NM_001370404.1:c.5114G>T NP_001357333.1:p.Arg1705Leu
NM_001370405.1:c.5105G>T NP_001357334.1:p.Arg1702Leu
NM_001077183.3:c.5045G>T NP_001070651.1:p.Arg1682Leu
NM_001114382.3:c.5177G>T NP_001107854.1:p.Arg1726Leu
NM_001318827.2:c.4937G>T NP_001305756.1:p.Arg1646Leu
NM_001318829.2:c.4901G>T NP_001305758.1:p.Arg1634Leu
NM_001318831.2:c.4514G>T NP_001305760.1:p.Arg1505Leu
NM_001318832.2:c.5078G>T NP_001305761.1:p.Arg1693Leu
NM_001363528.2:c.5048G>T NP_001350457.1:p.Arg1683Leu
NM_021055.3:c.5117G>T NP_066399.2:p.Arg1706Leu