Canonical Allele Identifier: CA2202032016
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088273A= , CM000678.2:g.2088273A= GRCh38
NC_000016.9:g.2138274A= , CM000678.1:g.2138274A= GRCh37
NC_000016.8:g.2078275A= NCBI36
NG_005895.1:g.43968A= , LRG_487:g.43968A=
NG_008617.1:g.54948T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3556A= ENSP00000455997.2:n.*3556A=
ENST00000642206.2:c.5054A= ENSP00000495146.2:p.Tyr1685=
ENST00000642365.2:c.5204A= ENSP00000495459.2:p.Tyr1735=
ENST00000644417.2:c.*5720A= ENSP00000493912.2:n.*5720A=
ENST00000646464.2:c.*7956A= ENSP00000496610.2:n.*7956A=
ENST00000219476.9:c.5207A= MANE Select ENSP00000219476.3:p.Tyr1736=
ENST00000350773.9:c.5138A= ENSP00000344383.4:p.Tyr1713=
ENST00000401874.7:c.5006A= ENSP00000384468.2:p.Tyr1669=
ENST00000568454.6:c.5039A= ENSP00000454487.1:p.Tyr1680=
ENST00000569110.2:c.1430A=
ENST00000569930.2:n.3089A=
ENST00000642365.1:c.3861A=
ENST00000642561.1:c.5066A= ENSP00000495099.1:p.Tyr1689=
ENST00000642791.1:n.804A=
ENST00000642797.1:c.5009A= ENSP00000493846.1:p.Tyr1670=
ENST00000642936.1:c.5075A= ENSP00000494514.1:p.Tyr1692=
ENST00000643088.1:c.5000A= ENSP00000494747.1:p.Tyr1667=
ENST00000643426.1:n.2855A=
ENST00000643946.1:c.5132A= ENSP00000495927.1:p.Tyr1711=
ENST00000644043.1:c.5078A= ENSP00000496262.1:p.Tyr1693=
ENST00000644329.1:c.5093A= ENSP00000496611.1:p.Tyr1698=
ENST00000644335.1:c.5003A= ENSP00000496317.1:p.Tyr1668=
ENST00000644399.1:c.5128A=
ENST00000645024.1:n.3291A=
ENST00000646388.1:c.5201A= ENSP00000495921.1:p.Tyr1734=
ENST00000646634.1:n.4022A=
ENST00000646674.1:n.2459A=
ENST00000647042.1:n.2430A=
ENST00000647180.1:n.2320A=
ENST00000219476.7:c.5207A= ENSP00000219476.3:p.Tyr1736=
ENST00000350773.8:c.5138A= ENSP00000344383.4:p.Tyr1713=
ENST00000382538.10:c.4862A= ENSP00000371978.6:p.Tyr1621=
ENST00000401874.6:c.5006A= ENSP00000384468.2:p.Tyr1669=
ENST00000439117.6:c.*4374A= ENSP00000406980.2:n.*4374A=
ENST00000439673.6:c.4898A= ENSP00000399232.2:p.Tyr1633=
ENST00000497886.5:n.2930A=
ENST00000568454.5:c.5039A= ENSP00000454487.1:p.Tyr1680=
ENST00000569110.1:c.1389A=
ENST00000569930.1:n.2322A=
NM_000548.3:c.5207A= , LRG_487t1:c.5207A= NP_000539.2:p.Tyr1736=
NM_001077183.1:c.5006A= NP_001070651.1:p.Tyr1669=
NM_001114382.1:c.5138A= NP_001107854.1:p.Tyr1713=
XM_005255529.3:c.5078A= XP_005255586.2:p.Tyr1693=
XM_005255531.3:c.5009A= XP_005255588.2:p.Tyr1670=
XM_011522636.1:c.5261A= XP_011520938.1:p.Tyr1754=
XM_011522637.1:c.5258A= XP_011520939.1:p.Tyr1753=
XM_011522638.1:c.5150A= XP_011520940.1:p.Tyr1717=
XM_011522639.1:c.5132A= XP_011520941.1:p.Tyr1711=
XM_011522640.1:c.5129A= XP_011520942.1:p.Tyr1710=
XM_011522641.1:c.4898A= XP_011520943.1:p.Tyr1633=
NM_000548.4:c.5207A= NP_000539.2:p.Tyr1736=
NM_001077183.2:c.5006A= NP_001070651.1:p.Tyr1669=
NM_001114382.2:c.5138A= NP_001107854.1:p.Tyr1713=
NM_001318827.1:c.4898A= NP_001305756.1:p.Tyr1633=
NM_001318829.1:c.4862A= NP_001305758.1:p.Tyr1621=
NM_001318831.1:c.4475A= NP_001305760.1:p.Tyr1492=
NM_001318832.1:c.5039A= NP_001305761.1:p.Tyr1680=
NM_001363528.1:c.5009A= NP_001350457.1:p.Tyr1670=
NM_021055.2:c.5078A= NP_066399.2:p.Tyr1693=
XM_005255531.4:c.5009A= XP_005255588.2:p.Tyr1670=
XM_011522636.2:c.5261A= XP_011520938.1:p.Tyr1754=
XM_011522637.2:c.5258A= XP_011520939.1:p.Tyr1753=
XM_011522638.2:c.5423A= XP_011520940.2:p.Tyr1808=
XM_011522639.2:c.5132A= XP_011520941.1:p.Tyr1711=
XM_011522640.2:c.5129A= XP_011520942.1:p.Tyr1710=
XM_017023615.1:c.5204A= XP_016879104.1:p.Tyr1735=
XM_017023616.1:c.5075A= XP_016879105.1:p.Tyr1692=
XM_017023617.1:c.5171A= XP_016879106.1:p.Tyr1724=
XM_017023618.1:c.3917A= XP_016879107.1:p.Tyr1306=
XM_024450413.1:c.5093A= XP_024306181.1:p.Tyr1698=
NM_000548.5:c.5207A= MANE Select NP_000539.2:p.Tyr1736=
NM_001370404.1:c.5075A= NP_001357333.1:p.Tyr1692=
NM_001370405.1:c.5066A= NP_001357334.1:p.Tyr1689=
NM_001077183.3:c.5006A= NP_001070651.1:p.Tyr1669=
NM_001114382.3:c.5138A= NP_001107854.1:p.Tyr1713=
NM_001318827.2:c.4898A= NP_001305756.1:p.Tyr1633=
NM_001318829.2:c.4862A= NP_001305758.1:p.Tyr1621=
NM_001318831.2:c.4475A= NP_001305760.1:p.Tyr1492=
NM_001318832.2:c.5039A= NP_001305761.1:p.Tyr1680=
NM_001363528.2:c.5009A= NP_001350457.1:p.Tyr1670=
NM_021055.3:c.5078A= NP_066399.2:p.Tyr1693=