Canonical Allele Identifier: CA2202032696
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088320C= , CM000678.2:g.2088320C= GRCh38
NC_000016.9:g.2138321C= , CM000678.1:g.2138321C= GRCh37
NC_000016.8:g.2078322C= NCBI36
NG_005895.1:g.44015C= , LRG_487:g.44015C=
NG_008617.1:g.54901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3603C= ENSP00000455997.2:n.*3603C=
ENST00000642206.2:c.5101C= ENSP00000495146.2:p.Gln1701=
ENST00000642365.2:c.5251C= ENSP00000495459.2:p.Gln1751=
ENST00000644417.2:c.*5767C= ENSP00000493912.2:n.*5767C=
ENST00000646464.2:c.*8003C= ENSP00000496610.2:n.*8003C=
ENST00000219476.9:c.5254C= MANE Select ENSP00000219476.3:p.Gln1752=
ENST00000350773.9:c.5185C= ENSP00000344383.4:p.Gln1729=
ENST00000401874.7:c.5053C= ENSP00000384468.2:p.Gln1685=
ENST00000568454.6:c.5086C= ENSP00000454487.1:p.Gln1696=
ENST00000569110.2:c.1477C=
ENST00000569930.2:n.3136C=
ENST00000642365.1:c.3908C=
ENST00000642561.1:c.5113C= ENSP00000495099.1:p.Gln1705=
ENST00000642791.1:n.851C=
ENST00000642797.1:c.5056C= ENSP00000493846.1:p.Gln1686=
ENST00000642936.1:c.5122C= ENSP00000494514.1:p.Gln1708=
ENST00000643088.1:c.5047C= ENSP00000494747.1:p.Gln1683=
ENST00000643426.1:n.2902C=
ENST00000643946.1:c.5179C= ENSP00000495927.1:p.Gln1727=
ENST00000644043.1:c.5125C= ENSP00000496262.1:p.Gln1709=
ENST00000644329.1:c.5140C= ENSP00000496611.1:p.Gln1714=
ENST00000644335.1:c.5050C= ENSP00000496317.1:p.Gln1684=
ENST00000644399.1:c.5175C=
ENST00000645024.1:n.3338C=
ENST00000646388.1:c.5248C= ENSP00000495921.1:p.Gln1750=
ENST00000646634.1:n.4069C=
ENST00000646674.1:n.2506C=
ENST00000647042.1:n.2477C=
ENST00000647180.1:n.2367C=
ENST00000219476.7:c.5254C= ENSP00000219476.3:p.Gln1752=
ENST00000350773.8:c.5185C= ENSP00000344383.4:p.Gln1729=
ENST00000382538.10:c.4909C= ENSP00000371978.6:p.Gln1637=
ENST00000401874.6:c.5053C= ENSP00000384468.2:p.Gln1685=
ENST00000439117.6:c.*4421C= ENSP00000406980.2:n.*4421C=
ENST00000439673.6:c.4945C= ENSP00000399232.2:p.Gln1649=
ENST00000497886.5:n.2977C=
ENST00000568454.5:c.5086C= ENSP00000454487.1:p.Gln1696=
ENST00000569110.1:c.1436C=
ENST00000569930.1:n.2369C=
NM_000548.3:c.5254C= , LRG_487t1:c.5254C= NP_000539.2:p.Gln1752=
NM_001077183.1:c.5053C= NP_001070651.1:p.Gln1685=
NM_001114382.1:c.5185C= NP_001107854.1:p.Gln1729=
XM_005255529.3:c.5125C= XP_005255586.2:p.Gln1709=
XM_005255531.3:c.5056C= XP_005255588.2:p.Gln1686=
XM_011522636.1:c.5308C= XP_011520938.1:p.Gln1770=
XM_011522637.1:c.5305C= XP_011520939.1:p.Gln1769=
XM_011522638.1:c.5197C= XP_011520940.1:p.Gln1733=
XM_011522639.1:c.5179C= XP_011520941.1:p.Gln1727=
XM_011522640.1:c.5176C= XP_011520942.1:p.Gln1726=
XM_011522641.1:c.4945C= XP_011520943.1:p.Gln1649=
NM_000548.4:c.5254C= NP_000539.2:p.Gln1752=
NM_001077183.2:c.5053C= NP_001070651.1:p.Gln1685=
NM_001114382.2:c.5185C= NP_001107854.1:p.Gln1729=
NM_001318827.1:c.4945C= NP_001305756.1:p.Gln1649=
NM_001318829.1:c.4909C= NP_001305758.1:p.Gln1637=
NM_001318831.1:c.4522C= NP_001305760.1:p.Gln1508=
NM_001318832.1:c.5086C= NP_001305761.1:p.Gln1696=
NM_001363528.1:c.5056C= NP_001350457.1:p.Gln1686=
NM_021055.2:c.5125C= NP_066399.2:p.Gln1709=
XM_005255531.4:c.5056C= XP_005255588.2:p.Gln1686=
XM_011522636.2:c.5308C= XP_011520938.1:p.Gln1770=
XM_011522637.2:c.5305C= XP_011520939.1:p.Gln1769=
XM_011522638.2:c.5470C= XP_011520940.2:p.Gln1824=
XM_011522639.2:c.5179C= XP_011520941.1:p.Gln1727=
XM_011522640.2:c.5176C= XP_011520942.1:p.Gln1726=
XM_017023615.1:c.5251C= XP_016879104.1:p.Gln1751=
XM_017023616.1:c.5122C= XP_016879105.1:p.Gln1708=
XM_017023617.1:c.5218C= XP_016879106.1:p.Gln1740=
XM_017023618.1:c.3964C= XP_016879107.1:p.Gln1322=
XM_024450413.1:c.5140C= XP_024306181.1:p.Gln1714=
NM_000548.5:c.5254C= MANE Select NP_000539.2:p.Gln1752=
NM_001370404.1:c.5122C= NP_001357333.1:p.Gln1708=
NM_001370405.1:c.5113C= NP_001357334.1:p.Gln1705=
NM_001077183.3:c.5053C= NP_001070651.1:p.Gln1685=
NM_001114382.3:c.5185C= NP_001107854.1:p.Gln1729=
NM_001318827.2:c.4945C= NP_001305756.1:p.Gln1649=
NM_001318829.2:c.4909C= NP_001305758.1:p.Gln1637=
NM_001318831.2:c.4522C= NP_001305760.1:p.Gln1508=
NM_001318832.2:c.5086C= NP_001305761.1:p.Gln1696=
NM_001363528.2:c.5056C= NP_001350457.1:p.Gln1686=
NM_021055.3:c.5125C= NP_066399.2:p.Gln1709=