Canonical Allele Identifier: CA2202044839
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084547A= , CM000678.2:g.2084547A= GRCh38
NC_000016.9:g.2134548A= , CM000678.1:g.2134548A= GRCh37
NC_000016.8:g.2074549A= NCBI36
NG_005895.1:g.40242A= , LRG_487:g.40242A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2674A= ENSP00000455997.2:n.*2674A=
ENST00000642206.2:c.4172A= ENSP00000495146.2:p.Glu1391=
ENST00000642365.2:c.4322A= ENSP00000495459.2:p.Glu1441=
ENST00000644417.2:c.*4705A= ENSP00000493912.2:n.*4705A=
ENST00000646464.2:c.*7074A= ENSP00000496610.2:n.*7074A=
ENST00000219476.9:c.4325A= MANE Select ENSP00000219476.3:p.Glu1442=
ENST00000350773.9:c.4256A= ENSP00000344383.4:p.Glu1419=
ENST00000401874.7:c.4124A= ENSP00000384468.2:p.Glu1375=
ENST00000568454.6:c.4157A= ENSP00000454487.1:p.Glu1386=
ENST00000569110.2:c.561A=
ENST00000569930.2:n.2207A=
ENST00000642365.1:c.2979A=
ENST00000642561.1:c.4196A= ENSP00000495099.1:p.Glu1399=
ENST00000642728.1:n.507A=
ENST00000642797.1:c.4127A= ENSP00000493846.1:p.Glu1376=
ENST00000642936.1:c.4193A= ENSP00000494514.1:p.Glu1398=
ENST00000643088.1:c.4124A= ENSP00000494747.1:p.Glu1375=
ENST00000643177.1:n.339A=
ENST00000643426.1:n.1973A=
ENST00000643946.1:c.4256A= ENSP00000495927.1:p.Glu1419=
ENST00000644043.1:c.4196A= ENSP00000496262.1:p.Glu1399=
ENST00000644329.1:c.4124A= ENSP00000496611.1:p.Glu1375=
ENST00000644335.1:c.4127A= ENSP00000496317.1:p.Glu1376=
ENST00000644399.1:c.4246A=
ENST00000645024.1:n.2409A=
ENST00000646388.1:c.4325A= ENSP00000495921.1:p.Glu1442=
ENST00000646634.1:n.3140A=
ENST00000646674.1:n.1577A=
ENST00000647042.1:n.1548A=
ENST00000647180.1:n.1438A=
ENST00000219476.7:c.4325A= ENSP00000219476.3:p.Glu1442=
ENST00000350773.8:c.4256A= ENSP00000344383.4:p.Glu1419=
ENST00000382538.10:c.3980A= ENSP00000371978.6:p.Glu1327=
ENST00000401874.6:c.4124A= ENSP00000384468.2:p.Glu1375=
ENST00000439117.6:c.*3492A= ENSP00000406980.2:n.*3492A=
ENST00000439673.6:c.4016A= ENSP00000399232.2:p.Glu1339=
ENST00000497886.5:n.2083A=
ENST00000568454.5:c.4157A= ENSP00000454487.1:p.Glu1386=
ENST00000569110.1:c.507A=
ENST00000569930.1:n.1440A=
NM_000548.3:c.4325A= , LRG_487t1:c.4325A= NP_000539.2:p.Glu1442=
NM_001077183.1:c.4124A= NP_001070651.1:p.Glu1375=
NM_001114382.1:c.4256A= NP_001107854.1:p.Glu1419=
XM_005255529.3:c.4196A= XP_005255586.2:p.Glu1399=
XM_005255531.3:c.4127A= XP_005255588.2:p.Glu1376=
XM_011522636.1:c.4379A= XP_011520938.1:p.Glu1460=
XM_011522637.1:c.4376A= XP_011520939.1:p.Glu1459=
XM_011522638.1:c.4268A= XP_011520940.1:p.Glu1423=
XM_011522639.1:c.4250A= XP_011520941.1:p.Glu1417=
XM_011522640.1:c.4247A= XP_011520942.1:p.Glu1416=
XM_011522641.1:c.4016A= XP_011520943.1:p.Glu1339=
NM_000548.4:c.4325A= NP_000539.2:p.Glu1442=
NM_001077183.2:c.4124A= NP_001070651.1:p.Glu1375=
NM_001114382.2:c.4256A= NP_001107854.1:p.Glu1419=
NM_001318827.1:c.4016A= NP_001305756.1:p.Glu1339=
NM_001318829.1:c.3980A= NP_001305758.1:p.Glu1327=
NM_001318831.1:c.3593A= NP_001305760.1:p.Glu1198=
NM_001318832.1:c.4157A= NP_001305761.1:p.Glu1386=
NM_001363528.1:c.4127A= NP_001350457.1:p.Glu1376=
NM_021055.2:c.4196A= NP_066399.2:p.Glu1399=
XM_005255531.4:c.4127A= XP_005255588.2:p.Glu1376=
XM_011522636.2:c.4379A= XP_011520938.1:p.Glu1460=
XM_011522637.2:c.4376A= XP_011520939.1:p.Glu1459=
XM_011522638.2:c.4541A= XP_011520940.2:p.Glu1514=
XM_011522639.2:c.4250A= XP_011520941.1:p.Glu1417=
XM_011522640.2:c.4247A= XP_011520942.1:p.Glu1416=
XM_017023615.1:c.4322A= XP_016879104.1:p.Glu1441=
XM_017023616.1:c.4193A= XP_016879105.1:p.Glu1398=
XM_017023617.1:c.4289A= XP_016879106.1:p.Glu1430=
XM_017023618.1:c.3035A= XP_016879107.1:p.Glu1012=
XM_024450413.1:c.4124A= XP_024306181.1:p.Glu1375=
NM_000548.5:c.4325A= MANE Select NP_000539.2:p.Glu1442=
NM_001370404.1:c.4193A= NP_001357333.1:p.Glu1398=
NM_001370405.1:c.4196A= NP_001357334.1:p.Glu1399=
NM_001077183.3:c.4124A= NP_001070651.1:p.Glu1375=
NM_001114382.3:c.4256A= NP_001107854.1:p.Glu1419=
NM_001318827.2:c.4016A= NP_001305756.1:p.Glu1339=
NM_001318829.2:c.3980A= NP_001305758.1:p.Glu1327=
NM_001318831.2:c.3593A= NP_001305760.1:p.Glu1198=
NM_001318832.2:c.4157A= NP_001305761.1:p.Glu1386=
NM_001363528.2:c.4127A= NP_001350457.1:p.Glu1376=
NM_021055.3:c.4196A= NP_066399.2:p.Glu1399=