Canonical Allele Identifier: CA394304750
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151551960

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085276C>T , CM000678.2:g.2085276C>T GRCh38
NC_000016.9:g.2135277C>T , CM000678.1:g.2135277C>T GRCh37
NC_000016.8:g.2075278C>T NCBI36
NG_005895.1:g.40971C>T , LRG_487:g.40971C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2965C>T ENSP00000455997.2:n.*2965C>T
ENST00000642206.2:c.4463C>T ENSP00000495146.2:p.Ser1488Leu
ENST00000642365.2:c.4613C>T ENSP00000495459.2:p.Ser1538Leu
ENST00000644417.2:c.*4996C>T ENSP00000493912.2:n.*4996C>T
ENST00000646464.2:c.*7365C>T ENSP00000496610.2:n.*7365C>T
ENST00000219476.9:c.4616C>T MANE Select ENSP00000219476.3:p.Ser1539Leu
ENST00000350773.9:c.4547C>T ENSP00000344383.4:p.Ser1516Leu
ENST00000401874.7:c.4415C>T ENSP00000384468.2:p.Ser1472Leu
ENST00000568454.6:c.4448C>T ENSP00000454487.1:p.Ser1483Leu
ENST00000569110.2:c.839C>T
ENST00000569930.2:n.2498C>T
ENST00000642365.1:c.3270C>T
ENST00000642561.1:c.4487C>T ENSP00000495099.1:p.Ser1496Leu
ENST00000642728.1:n.798C>T
ENST00000642791.1:n.213C>T
ENST00000642797.1:c.4418C>T ENSP00000493846.1:p.Ser1473Leu
ENST00000642936.1:c.4484C>T ENSP00000494514.1:p.Ser1495Leu
ENST00000643088.1:c.4409C>T ENSP00000494747.1:p.Ser1470Leu
ENST00000643177.1:n.630C>T
ENST00000643426.1:n.2264C>T
ENST00000643946.1:c.4541C>T ENSP00000495927.1:p.Ser1514Leu
ENST00000644043.1:c.4487C>T ENSP00000496262.1:p.Ser1496Leu
ENST00000644278.1:n.98C>T
ENST00000644329.1:c.4415C>T ENSP00000496611.1:p.Ser1472Leu
ENST00000644335.1:c.4412C>T ENSP00000496317.1:p.Ser1471Leu
ENST00000644399.1:c.4537C>T
ENST00000645024.1:n.2700C>T
ENST00000646388.1:c.4610C>T ENSP00000495921.1:p.Ser1537Leu
ENST00000646634.1:n.3431C>T
ENST00000646674.1:n.1868C>T
ENST00000647042.1:n.1839C>T
ENST00000647180.1:n.1729C>T
ENST00000219476.7:c.4616C>T ENSP00000219476.3:p.Ser1539Leu
ENST00000350773.8:c.4547C>T ENSP00000344383.4:p.Ser1516Leu
ENST00000382538.10:c.4271C>T ENSP00000371978.6:p.Ser1424Leu
ENST00000401874.6:c.4415C>T ENSP00000384468.2:p.Ser1472Leu
ENST00000439117.6:c.*3783C>T ENSP00000406980.2:n.*3783C>T
ENST00000439673.6:c.4307C>T ENSP00000399232.2:p.Ser1436Leu
ENST00000497886.5:n.2374C>T
ENST00000568454.5:c.4448C>T ENSP00000454487.1:p.Ser1483Leu
ENST00000569110.1:c.798C>T
ENST00000569930.1:n.1731C>T
NM_000548.3:c.4616C>T , LRG_487t1:c.4616C>T NP_000539.2:p.Ser1539Leu
NM_001077183.1:c.4415C>T NP_001070651.1:p.Ser1472Leu
NM_001114382.1:c.4547C>T NP_001107854.1:p.Ser1516Leu
XM_005255529.3:c.4487C>T XP_005255586.2:p.Ser1496Leu
XM_005255531.3:c.4418C>T XP_005255588.2:p.Ser1473Leu
XM_011522636.1:c.4670C>T XP_011520938.1:p.Ser1557Leu
XM_011522637.1:c.4667C>T XP_011520939.1:p.Ser1556Leu
XM_011522638.1:c.4559C>T XP_011520940.1:p.Ser1520Leu
XM_011522639.1:c.4541C>T XP_011520941.1:p.Ser1514Leu
XM_011522640.1:c.4538C>T XP_011520942.1:p.Ser1513Leu
XM_011522641.1:c.4307C>T XP_011520943.1:p.Ser1436Leu
NM_000548.4:c.4616C>T NP_000539.2:p.Ser1539Leu
NM_001077183.2:c.4415C>T NP_001070651.1:p.Ser1472Leu
NM_001114382.2:c.4547C>T NP_001107854.1:p.Ser1516Leu
NM_001318827.1:c.4307C>T NP_001305756.1:p.Ser1436Leu
NM_001318829.1:c.4271C>T NP_001305758.1:p.Ser1424Leu
NM_001318831.1:c.3884C>T NP_001305760.1:p.Ser1295Leu
NM_001318832.1:c.4448C>T NP_001305761.1:p.Ser1483Leu
NM_001363528.1:c.4418C>T NP_001350457.1:p.Ser1473Leu
NM_021055.2:c.4487C>T NP_066399.2:p.Ser1496Leu
XM_005255531.4:c.4418C>T XP_005255588.2:p.Ser1473Leu
XM_011522636.2:c.4670C>T XP_011520938.1:p.Ser1557Leu
XM_011522637.2:c.4667C>T XP_011520939.1:p.Ser1556Leu
XM_011522638.2:c.4832C>T XP_011520940.2:p.Ser1611Leu
XM_011522639.2:c.4541C>T XP_011520941.1:p.Ser1514Leu
XM_011522640.2:c.4538C>T XP_011520942.1:p.Ser1513Leu
XM_017023615.1:c.4613C>T XP_016879104.1:p.Ser1538Leu
XM_017023616.1:c.4484C>T XP_016879105.1:p.Ser1495Leu
XM_017023617.1:c.4580C>T XP_016879106.1:p.Ser1527Leu
XM_017023618.1:c.3326C>T XP_016879107.1:p.Ser1109Leu
XM_024450413.1:c.4415C>T XP_024306181.1:p.Ser1472Leu
NM_000548.5:c.4616C>T MANE Select NP_000539.2:p.Ser1539Leu
NM_001370404.1:c.4484C>T NP_001357333.1:p.Ser1495Leu
NM_001370405.1:c.4487C>T NP_001357334.1:p.Ser1496Leu
NM_001077183.3:c.4415C>T NP_001070651.1:p.Ser1472Leu
NM_001114382.3:c.4547C>T NP_001107854.1:p.Ser1516Leu
NM_001318827.2:c.4307C>T NP_001305756.1:p.Ser1436Leu
NM_001318829.2:c.4271C>T NP_001305758.1:p.Ser1424Leu
NM_001318831.2:c.3884C>T NP_001305760.1:p.Ser1295Leu
NM_001318832.2:c.4448C>T NP_001305761.1:p.Ser1483Leu
NM_001363528.2:c.4418C>T NP_001350457.1:p.Ser1473Leu
NM_021055.3:c.4487C>T NP_066399.2:p.Ser1496Leu