Canonical Allele Identifier: CA394315249
Gene: TSC2 HGNC NCBI

Linked Data

gnomAD v4: 16-2088473-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088473C>A , CM000678.2:g.2088473C>A GRCh38
NC_000016.9:g.2138474C>A , CM000678.1:g.2138474C>A GRCh37
NC_000016.8:g.2078475C>A NCBI36
NG_005895.1:g.44168C>A , LRG_487:g.44168C>A
NG_008617.1:g.54748G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3636C>A ENSP00000455997.2:n.*3636C>A
ENST00000642206.2:c.5134C>A ENSP00000495146.2:p.Pro1712Thr
ENST00000642365.2:c.5284C>A ENSP00000495459.2:p.Pro1762Thr
ENST00000644417.2:c.*5800C>A ENSP00000493912.2:n.*5800C>A
ENST00000646464.2:c.*8036C>A ENSP00000496610.2:n.*8036C>A
ENST00000219476.9:c.5287C>A MANE Select ENSP00000219476.3:p.Pro1763Thr
ENST00000350773.9:c.5218C>A ENSP00000344383.4:p.Pro1740Thr
ENST00000401874.7:c.5086C>A ENSP00000384468.2:p.Pro1696Thr
ENST00000568454.6:c.5119C>A ENSP00000454487.1:p.Pro1707Thr
ENST00000569110.2:c.1510C>A
ENST00000569930.2:n.3169C>A
ENST00000642365.1:c.3941C>A
ENST00000642561.1:c.5146C>A ENSP00000495099.1:p.Pro1716Thr
ENST00000642791.1:n.884C>A
ENST00000642797.1:c.5089C>A ENSP00000493846.1:p.Pro1697Thr
ENST00000642936.1:c.5155C>A ENSP00000494514.1:p.Pro1719Thr
ENST00000643088.1:c.5080C>A ENSP00000494747.1:p.Pro1694Thr
ENST00000643426.1:n.2935C>A
ENST00000643946.1:c.5212C>A ENSP00000495927.1:p.Pro1738Thr
ENST00000644043.1:c.5158C>A ENSP00000496262.1:p.Pro1720Thr
ENST00000644329.1:c.5173C>A ENSP00000496611.1:p.Pro1725Thr
ENST00000644335.1:c.5083C>A ENSP00000496317.1:p.Pro1695Thr
ENST00000644399.1:c.5208C>A
ENST00000645024.1:n.3371C>A
ENST00000646388.1:c.5281C>A ENSP00000495921.1:p.Pro1761Thr
ENST00000646634.1:n.4102C>A
ENST00000646674.1:n.2539C>A
ENST00000647042.1:n.2510C>A
ENST00000647180.1:n.2400C>A
ENST00000219476.7:c.5287C>A ENSP00000219476.3:p.Pro1763Thr
ENST00000350773.8:c.5218C>A ENSP00000344383.4:p.Pro1740Thr
ENST00000382538.10:c.4942C>A ENSP00000371978.6:p.Pro1648Thr
ENST00000401874.6:c.5086C>A ENSP00000384468.2:p.Pro1696Thr
ENST00000439117.6:c.*4454C>A ENSP00000406980.2:n.*4454C>A
ENST00000439673.6:c.4978C>A ENSP00000399232.2:p.Pro1660Thr
ENST00000497886.5:n.3010C>A
ENST00000568454.5:c.5119C>A ENSP00000454487.1:p.Pro1707Thr
ENST00000569110.1:c.1469C>A
ENST00000569930.1:n.2402C>A
NM_000548.3:c.5287C>A , LRG_487t1:c.5287C>A NP_000539.2:p.Pro1763Thr
NM_001077183.1:c.5086C>A NP_001070651.1:p.Pro1696Thr
NM_001114382.1:c.5218C>A NP_001107854.1:p.Pro1740Thr
XM_005255529.3:c.5158C>A XP_005255586.2:p.Pro1720Thr
XM_005255531.3:c.5089C>A XP_005255588.2:p.Pro1697Thr
XM_011522636.1:c.5341C>A XP_011520938.1:p.Pro1781Thr
XM_011522637.1:c.5338C>A XP_011520939.1:p.Pro1780Thr
XM_011522638.1:c.5230C>A XP_011520940.1:p.Pro1744Thr
XM_011522639.1:c.5212C>A XP_011520941.1:p.Pro1738Thr
XM_011522640.1:c.5209C>A XP_011520942.1:p.Pro1737Thr
XM_011522641.1:c.4978C>A XP_011520943.1:p.Pro1660Thr
NM_000548.4:c.5287C>A NP_000539.2:p.Pro1763Thr
NM_001077183.2:c.5086C>A NP_001070651.1:p.Pro1696Thr
NM_001114382.2:c.5218C>A NP_001107854.1:p.Pro1740Thr
NM_001318827.1:c.4978C>A NP_001305756.1:p.Pro1660Thr
NM_001318829.1:c.4942C>A NP_001305758.1:p.Pro1648Thr
NM_001318831.1:c.4555C>A NP_001305760.1:p.Pro1519Thr
NM_001318832.1:c.5119C>A NP_001305761.1:p.Pro1707Thr
NM_001363528.1:c.5089C>A NP_001350457.1:p.Pro1697Thr
NM_021055.2:c.5158C>A NP_066399.2:p.Pro1720Thr
XM_005255531.4:c.5089C>A XP_005255588.2:p.Pro1697Thr
XM_011522636.2:c.5341C>A XP_011520938.1:p.Pro1781Thr
XM_011522637.2:c.5338C>A XP_011520939.1:p.Pro1780Thr
XM_011522638.2:c.5503C>A XP_011520940.2:p.Pro1835Thr
XM_011522639.2:c.5212C>A XP_011520941.1:p.Pro1738Thr
XM_011522640.2:c.5209C>A XP_011520942.1:p.Pro1737Thr
XM_017023615.1:c.5284C>A XP_016879104.1:p.Pro1762Thr
XM_017023616.1:c.5155C>A XP_016879105.1:p.Pro1719Thr
XM_017023617.1:c.5251C>A XP_016879106.1:p.Pro1751Thr
XM_017023618.1:c.3997C>A XP_016879107.1:p.Pro1333Thr
XM_024450413.1:c.5173C>A XP_024306181.1:p.Pro1725Thr
NM_000548.5:c.5287C>A MANE Select NP_000539.2:p.Pro1763Thr
NM_001370404.1:c.5155C>A NP_001357333.1:p.Pro1719Thr
NM_001370405.1:c.5146C>A NP_001357334.1:p.Pro1716Thr
NM_001077183.3:c.5086C>A NP_001070651.1:p.Pro1696Thr
NM_001114382.3:c.5218C>A NP_001107854.1:p.Pro1740Thr
NM_001318827.2:c.4978C>A NP_001305756.1:p.Pro1660Thr
NM_001318829.2:c.4942C>A NP_001305758.1:p.Pro1648Thr
NM_001318831.2:c.4555C>A NP_001305760.1:p.Pro1519Thr
NM_001318832.2:c.5119C>A NP_001305761.1:p.Pro1707Thr
NM_001363528.2:c.5089C>A NP_001350457.1:p.Pro1697Thr
NM_021055.3:c.5158C>A NP_066399.2:p.Pro1720Thr