Canonical Allele Identifier: CA2202031799
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088256C= , CM000678.2:g.2088256C= GRCh38
NC_000016.9:g.2138257C= , CM000678.1:g.2138257C= GRCh37
NC_000016.8:g.2078258C= NCBI36
NG_005895.1:g.43951C= , LRG_487:g.43951C=
NG_008617.1:g.54965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3539C= ENSP00000455997.2:n.*3539C=
ENST00000642206.2:c.5037C= ENSP00000495146.2:p.Ser1679=
ENST00000642365.2:c.5187C= ENSP00000495459.2:p.Ser1729=
ENST00000644417.2:c.*5703C= ENSP00000493912.2:n.*5703C=
ENST00000646464.2:c.*7939C= ENSP00000496610.2:n.*7939C=
ENST00000219476.9:c.5190C= MANE Select ENSP00000219476.3:p.Ser1730=
ENST00000350773.9:c.5121C= ENSP00000344383.4:p.Ser1707=
ENST00000401874.7:c.4989C= ENSP00000384468.2:p.Ser1663=
ENST00000568454.6:c.5022C= ENSP00000454487.1:p.Ser1674=
ENST00000569110.2:c.1413C=
ENST00000569930.2:n.3072C=
ENST00000642365.1:c.3844C=
ENST00000642561.1:c.5049C= ENSP00000495099.1:p.Ser1683=
ENST00000642791.1:n.787C=
ENST00000642797.1:c.4992C= ENSP00000493846.1:p.Ser1664=
ENST00000642936.1:c.5058C= ENSP00000494514.1:p.Ser1686=
ENST00000643088.1:c.4983C= ENSP00000494747.1:p.Ser1661=
ENST00000643426.1:n.2838C=
ENST00000643946.1:c.5115C= ENSP00000495927.1:p.Ser1705=
ENST00000644043.1:c.5061C= ENSP00000496262.1:p.Ser1687=
ENST00000644329.1:c.5076C= ENSP00000496611.1:p.Ser1692=
ENST00000644335.1:c.4986C= ENSP00000496317.1:p.Ser1662=
ENST00000644399.1:c.5111C=
ENST00000645024.1:n.3274C=
ENST00000646388.1:c.5184C= ENSP00000495921.1:p.Ser1728=
ENST00000646634.1:n.4005C=
ENST00000646674.1:n.2442C=
ENST00000647042.1:n.2413C=
ENST00000647180.1:n.2303C=
ENST00000219476.7:c.5190C= ENSP00000219476.3:p.Ser1730=
ENST00000350773.8:c.5121C= ENSP00000344383.4:p.Ser1707=
ENST00000382538.10:c.4845C= ENSP00000371978.6:p.Ser1615=
ENST00000401874.6:c.4989C= ENSP00000384468.2:p.Ser1663=
ENST00000439117.6:c.*4357C= ENSP00000406980.2:n.*4357C=
ENST00000439673.6:c.4881C= ENSP00000399232.2:p.Ser1627=
ENST00000497886.5:n.2913C=
ENST00000568454.5:c.5022C= ENSP00000454487.1:p.Ser1674=
ENST00000569110.1:c.1372C=
ENST00000569930.1:n.2305C=
NM_000548.3:c.5190C= , LRG_487t1:c.5190C= NP_000539.2:p.Ser1730=
NM_001077183.1:c.4989C= NP_001070651.1:p.Ser1663=
NM_001114382.1:c.5121C= NP_001107854.1:p.Ser1707=
XM_005255529.3:c.5061C= XP_005255586.2:p.Ser1687=
XM_005255531.3:c.4992C= XP_005255588.2:p.Ser1664=
XM_011522636.1:c.5244C= XP_011520938.1:p.Ser1748=
XM_011522637.1:c.5241C= XP_011520939.1:p.Ser1747=
XM_011522638.1:c.5133C= XP_011520940.1:p.Ser1711=
XM_011522639.1:c.5115C= XP_011520941.1:p.Ser1705=
XM_011522640.1:c.5112C= XP_011520942.1:p.Ser1704=
XM_011522641.1:c.4881C= XP_011520943.1:p.Ser1627=
NM_000548.4:c.5190C= NP_000539.2:p.Ser1730=
NM_001077183.2:c.4989C= NP_001070651.1:p.Ser1663=
NM_001114382.2:c.5121C= NP_001107854.1:p.Ser1707=
NM_001318827.1:c.4881C= NP_001305756.1:p.Ser1627=
NM_001318829.1:c.4845C= NP_001305758.1:p.Ser1615=
NM_001318831.1:c.4458C= NP_001305760.1:p.Ser1486=
NM_001318832.1:c.5022C= NP_001305761.1:p.Ser1674=
NM_001363528.1:c.4992C= NP_001350457.1:p.Ser1664=
NM_021055.2:c.5061C= NP_066399.2:p.Ser1687=
XM_005255531.4:c.4992C= XP_005255588.2:p.Ser1664=
XM_011522636.2:c.5244C= XP_011520938.1:p.Ser1748=
XM_011522637.2:c.5241C= XP_011520939.1:p.Ser1747=
XM_011522638.2:c.5406C= XP_011520940.2:p.Ser1802=
XM_011522639.2:c.5115C= XP_011520941.1:p.Ser1705=
XM_011522640.2:c.5112C= XP_011520942.1:p.Ser1704=
XM_017023615.1:c.5187C= XP_016879104.1:p.Ser1729=
XM_017023616.1:c.5058C= XP_016879105.1:p.Ser1686=
XM_017023617.1:c.5154C= XP_016879106.1:p.Ser1718=
XM_017023618.1:c.3900C= XP_016879107.1:p.Ser1300=
XM_024450413.1:c.5076C= XP_024306181.1:p.Ser1692=
NM_000548.5:c.5190C= MANE Select NP_000539.2:p.Ser1730=
NM_001370404.1:c.5058C= NP_001357333.1:p.Ser1686=
NM_001370405.1:c.5049C= NP_001357334.1:p.Ser1683=
NM_001077183.3:c.4989C= NP_001070651.1:p.Ser1663=
NM_001114382.3:c.5121C= NP_001107854.1:p.Ser1707=
NM_001318827.2:c.4881C= NP_001305756.1:p.Ser1627=
NM_001318829.2:c.4845C= NP_001305758.1:p.Ser1615=
NM_001318831.2:c.4458C= NP_001305760.1:p.Ser1486=
NM_001318832.2:c.5022C= NP_001305761.1:p.Ser1674=
NM_001363528.2:c.4992C= NP_001350457.1:p.Ser1664=
NM_021055.3:c.5061C= NP_066399.2:p.Ser1687=