Canonical Allele Identifier: CA394304428
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151550463

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085243A>G , CM000678.2:g.2085243A>G GRCh38
NC_000016.9:g.2135244A>G , CM000678.1:g.2135244A>G GRCh37
NC_000016.8:g.2075245A>G NCBI36
NG_005895.1:g.40938A>G , LRG_487:g.40938A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2932A>G ENSP00000455997.2:n.*2932A>G
ENST00000642206.2:c.4430A>G ENSP00000495146.2:p.Glu1477Gly
ENST00000642365.2:c.4580A>G ENSP00000495459.2:p.Glu1527Gly
ENST00000644417.2:c.*4963A>G ENSP00000493912.2:n.*4963A>G
ENST00000646464.2:c.*7332A>G ENSP00000496610.2:n.*7332A>G
ENST00000219476.9:c.4583A>G MANE Select ENSP00000219476.3:p.Glu1528Gly
ENST00000350773.9:c.4514A>G ENSP00000344383.4:p.Glu1505Gly
ENST00000401874.7:c.4382A>G ENSP00000384468.2:p.Glu1461Gly
ENST00000568454.6:c.4415A>G ENSP00000454487.1:p.Glu1472Gly
ENST00000569110.2:c.806A>G
ENST00000569930.2:n.2465A>G
ENST00000642365.1:c.3237A>G
ENST00000642561.1:c.4454A>G ENSP00000495099.1:p.Glu1485Gly
ENST00000642728.1:n.765A>G
ENST00000642791.1:n.180A>G
ENST00000642797.1:c.4385A>G ENSP00000493846.1:p.Glu1462Gly
ENST00000642936.1:c.4451A>G ENSP00000494514.1:p.Glu1484Gly
ENST00000643088.1:c.4376A>G ENSP00000494747.1:p.Glu1459Gly
ENST00000643177.1:n.597A>G
ENST00000643426.1:n.2231A>G
ENST00000643946.1:c.4508A>G ENSP00000495927.1:p.Glu1503Gly
ENST00000644043.1:c.4454A>G ENSP00000496262.1:p.Glu1485Gly
ENST00000644278.1:n.65A>G
ENST00000644329.1:c.4382A>G ENSP00000496611.1:p.Glu1461Gly
ENST00000644335.1:c.4379A>G ENSP00000496317.1:p.Glu1460Gly
ENST00000644399.1:c.4504A>G
ENST00000645024.1:n.2667A>G
ENST00000646388.1:c.4577A>G ENSP00000495921.1:p.Glu1526Gly
ENST00000646634.1:n.3398A>G
ENST00000646674.1:n.1835A>G
ENST00000647042.1:n.1806A>G
ENST00000647180.1:n.1696A>G
ENST00000219476.7:c.4583A>G ENSP00000219476.3:p.Glu1528Gly
ENST00000350773.8:c.4514A>G ENSP00000344383.4:p.Glu1505Gly
ENST00000382538.10:c.4238A>G ENSP00000371978.6:p.Glu1413Gly
ENST00000401874.6:c.4382A>G ENSP00000384468.2:p.Glu1461Gly
ENST00000439117.6:c.*3750A>G ENSP00000406980.2:n.*3750A>G
ENST00000439673.6:c.4274A>G ENSP00000399232.2:p.Glu1425Gly
ENST00000497886.5:n.2341A>G
ENST00000568454.5:c.4415A>G ENSP00000454487.1:p.Glu1472Gly
ENST00000569110.1:c.765A>G
ENST00000569930.1:n.1698A>G
NM_000548.3:c.4583A>G , LRG_487t1:c.4583A>G NP_000539.2:p.Glu1528Gly
NM_001077183.1:c.4382A>G NP_001070651.1:p.Glu1461Gly
NM_001114382.1:c.4514A>G NP_001107854.1:p.Glu1505Gly
XM_005255529.3:c.4454A>G XP_005255586.2:p.Glu1485Gly
XM_005255531.3:c.4385A>G XP_005255588.2:p.Glu1462Gly
XM_011522636.1:c.4637A>G XP_011520938.1:p.Glu1546Gly
XM_011522637.1:c.4634A>G XP_011520939.1:p.Glu1545Gly
XM_011522638.1:c.4526A>G XP_011520940.1:p.Glu1509Gly
XM_011522639.1:c.4508A>G XP_011520941.1:p.Glu1503Gly
XM_011522640.1:c.4505A>G XP_011520942.1:p.Glu1502Gly
XM_011522641.1:c.4274A>G XP_011520943.1:p.Glu1425Gly
NM_000548.4:c.4583A>G NP_000539.2:p.Glu1528Gly
NM_001077183.2:c.4382A>G NP_001070651.1:p.Glu1461Gly
NM_001114382.2:c.4514A>G NP_001107854.1:p.Glu1505Gly
NM_001318827.1:c.4274A>G NP_001305756.1:p.Glu1425Gly
NM_001318829.1:c.4238A>G NP_001305758.1:p.Glu1413Gly
NM_001318831.1:c.3851A>G NP_001305760.1:p.Glu1284Gly
NM_001318832.1:c.4415A>G NP_001305761.1:p.Glu1472Gly
NM_001363528.1:c.4385A>G NP_001350457.1:p.Glu1462Gly
NM_021055.2:c.4454A>G NP_066399.2:p.Glu1485Gly
XM_005255531.4:c.4385A>G XP_005255588.2:p.Glu1462Gly
XM_011522636.2:c.4637A>G XP_011520938.1:p.Glu1546Gly
XM_011522637.2:c.4634A>G XP_011520939.1:p.Glu1545Gly
XM_011522638.2:c.4799A>G XP_011520940.2:p.Glu1600Gly
XM_011522639.2:c.4508A>G XP_011520941.1:p.Glu1503Gly
XM_011522640.2:c.4505A>G XP_011520942.1:p.Glu1502Gly
XM_017023615.1:c.4580A>G XP_016879104.1:p.Glu1527Gly
XM_017023616.1:c.4451A>G XP_016879105.1:p.Glu1484Gly
XM_017023617.1:c.4547A>G XP_016879106.1:p.Glu1516Gly
XM_017023618.1:c.3293A>G XP_016879107.1:p.Glu1098Gly
XM_024450413.1:c.4382A>G XP_024306181.1:p.Glu1461Gly
NM_000548.5:c.4583A>G MANE Select NP_000539.2:p.Glu1528Gly
NM_001370404.1:c.4451A>G NP_001357333.1:p.Glu1484Gly
NM_001370405.1:c.4454A>G NP_001357334.1:p.Glu1485Gly
NM_001077183.3:c.4382A>G NP_001070651.1:p.Glu1461Gly
NM_001114382.3:c.4514A>G NP_001107854.1:p.Glu1505Gly
NM_001318827.2:c.4274A>G NP_001305756.1:p.Glu1425Gly
NM_001318829.2:c.4238A>G NP_001305758.1:p.Glu1413Gly
NM_001318831.2:c.3851A>G NP_001305760.1:p.Glu1284Gly
NM_001318832.2:c.4415A>G NP_001305761.1:p.Glu1472Gly
NM_001363528.2:c.4385A>G NP_001350457.1:p.Glu1462Gly
NM_021055.3:c.4454A>G NP_066399.2:p.Glu1485Gly