Canonical Allele Identifier: CA2202043435
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084250A= , CM000678.2:g.2084250A= GRCh38
NC_000016.9:g.2134251A= , CM000678.1:g.2134251A= GRCh37
NC_000016.8:g.2074252A= NCBI36
NG_005895.1:g.39945A= , LRG_487:g.39945A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2377A= ENSP00000455997.2:n.*2377A=
ENST00000642206.2:c.3875A= ENSP00000495146.2:p.Glu1292=
ENST00000642365.2:c.4025A= ENSP00000495459.2:p.Glu1342=
ENST00000644417.2:c.*4408A= ENSP00000493912.2:n.*4408A=
ENST00000646464.2:c.*6777A= ENSP00000496610.2:n.*6777A=
ENST00000219476.9:c.4028A= MANE Select ENSP00000219476.3:p.Glu1343=
ENST00000350773.9:c.3959A= ENSP00000344383.4:p.Glu1320=
ENST00000401874.7:c.3827A= ENSP00000384468.2:p.Glu1276=
ENST00000568454.6:c.3860A= ENSP00000454487.1:p.Glu1287=
ENST00000569110.2:c.264A=
ENST00000569930.2:n.1910A=
ENST00000642365.1:c.2682A=
ENST00000642561.1:c.3899A= ENSP00000495099.1:p.Glu1300=
ENST00000642728.1:n.210A=
ENST00000642797.1:c.3830A= ENSP00000493846.1:p.Glu1277=
ENST00000642936.1:c.3896A= ENSP00000494514.1:p.Glu1299=
ENST00000643088.1:c.3827A= ENSP00000494747.1:p.Glu1276=
ENST00000643177.1:n.42A=
ENST00000643426.1:n.1676A=
ENST00000643533.1:n.469A=
ENST00000643946.1:c.3959A= ENSP00000495927.1:p.Glu1320=
ENST00000644043.1:c.3899A= ENSP00000496262.1:p.Glu1300=
ENST00000644329.1:c.3827A= ENSP00000496611.1:p.Glu1276=
ENST00000644335.1:c.3830A= ENSP00000496317.1:p.Glu1277=
ENST00000644399.1:c.3949A=
ENST00000645024.1:n.2112A=
ENST00000645186.1:c.271A=
ENST00000646388.1:c.4028A= ENSP00000495921.1:p.Glu1343=
ENST00000646634.1:n.2843A=
ENST00000646674.1:n.1280A=
ENST00000647042.1:n.1251A=
ENST00000647180.1:n.1141A=
ENST00000219476.7:c.4028A= ENSP00000219476.3:p.Glu1343=
ENST00000350773.8:c.3959A= ENSP00000344383.4:p.Glu1320=
ENST00000382538.10:c.3683A= ENSP00000371978.6:p.Glu1228=
ENST00000401874.6:c.3827A= ENSP00000384468.2:p.Glu1276=
ENST00000439117.6:c.*3195A= ENSP00000406980.2:n.*3195A=
ENST00000439673.6:c.3719A= ENSP00000399232.2:p.Glu1240=
ENST00000497886.5:n.1786A=
ENST00000568454.5:c.3860A= ENSP00000454487.1:p.Glu1287=
ENST00000569110.1:c.210A=
ENST00000569930.1:n.1143A=
NM_000548.3:c.4028A= , LRG_487t1:c.4028A= NP_000539.2:p.Glu1343=
NM_001077183.1:c.3827A= NP_001070651.1:p.Glu1276=
NM_001114382.1:c.3959A= NP_001107854.1:p.Glu1320=
XM_005255529.3:c.3899A= XP_005255586.2:p.Glu1300=
XM_005255531.3:c.3830A= XP_005255588.2:p.Glu1277=
XM_011522636.1:c.4082A= XP_011520938.1:p.Glu1361=
XM_011522637.1:c.4079A= XP_011520939.1:p.Glu1360=
XM_011522638.1:c.3971A= XP_011520940.1:p.Glu1324=
XM_011522639.1:c.3953A= XP_011520941.1:p.Glu1318=
XM_011522640.1:c.3950A= XP_011520942.1:p.Glu1317=
XM_011522641.1:c.3719A= XP_011520943.1:p.Glu1240=
NM_000548.4:c.4028A= NP_000539.2:p.Glu1343=
NM_001077183.2:c.3827A= NP_001070651.1:p.Glu1276=
NM_001114382.2:c.3959A= NP_001107854.1:p.Glu1320=
NM_001318827.1:c.3719A= NP_001305756.1:p.Glu1240=
NM_001318829.1:c.3683A= NP_001305758.1:p.Glu1228=
NM_001318831.1:c.3296A= NP_001305760.1:p.Glu1099=
NM_001318832.1:c.3860A= NP_001305761.1:p.Glu1287=
NM_001363528.1:c.3830A= NP_001350457.1:p.Glu1277=
NM_021055.2:c.3899A= NP_066399.2:p.Glu1300=
XM_005255531.4:c.3830A= XP_005255588.2:p.Glu1277=
XM_011522636.2:c.4082A= XP_011520938.1:p.Glu1361=
XM_011522637.2:c.4079A= XP_011520939.1:p.Glu1360=
XM_011522638.2:c.4244A= XP_011520940.2:p.Glu1415=
XM_011522639.2:c.3953A= XP_011520941.1:p.Glu1318=
XM_011522640.2:c.3950A= XP_011520942.1:p.Glu1317=
XM_017023615.1:c.4025A= XP_016879104.1:p.Glu1342=
XM_017023616.1:c.3896A= XP_016879105.1:p.Glu1299=
XM_017023617.1:c.3992A= XP_016879106.1:p.Glu1331=
XM_017023618.1:c.2738A= XP_016879107.1:p.Glu913=
XM_024450413.1:c.3827A= XP_024306181.1:p.Glu1276=
NM_000548.5:c.4028A= MANE Select NP_000539.2:p.Glu1343=
NM_001370404.1:c.3896A= NP_001357333.1:p.Glu1299=
NM_001370405.1:c.3899A= NP_001357334.1:p.Glu1300=
NM_001077183.3:c.3827A= NP_001070651.1:p.Glu1276=
NM_001114382.3:c.3959A= NP_001107854.1:p.Glu1320=
NM_001318827.2:c.3719A= NP_001305756.1:p.Glu1240=
NM_001318829.2:c.3683A= NP_001305758.1:p.Glu1228=
NM_001318831.2:c.3296A= NP_001305760.1:p.Glu1099=
NM_001318832.2:c.3860A= NP_001305761.1:p.Glu1287=
NM_001363528.2:c.3830A= NP_001350457.1:p.Glu1277=
NM_021055.3:c.3899A= NP_066399.2:p.Glu1300=