Canonical Allele Identifier: CA2202044427
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084445G= , CM000678.2:g.2084445G= GRCh38
NC_000016.9:g.2134446G= , CM000678.1:g.2134446G= GRCh37
NC_000016.8:g.2074447G= NCBI36
NG_005895.1:g.40140G= , LRG_487:g.40140G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2572G= ENSP00000455997.2:n.*2572G=
ENST00000642206.2:c.4070G= ENSP00000495146.2:p.Gly1357=
ENST00000642365.2:c.4220G= ENSP00000495459.2:p.Gly1407=
ENST00000644417.2:c.*4603G= ENSP00000493912.2:n.*4603G=
ENST00000646464.2:c.*6972G= ENSP00000496610.2:n.*6972G=
ENST00000219476.9:c.4223G= MANE Select ENSP00000219476.3:p.Gly1408=
ENST00000350773.9:c.4154G= ENSP00000344383.4:p.Gly1385=
ENST00000401874.7:c.4022G= ENSP00000384468.2:p.Gly1341=
ENST00000568454.6:c.4055G= ENSP00000454487.1:p.Gly1352=
ENST00000569110.2:c.459G=
ENST00000569930.2:n.2105G=
ENST00000642365.1:c.2877G=
ENST00000642561.1:c.4094G= ENSP00000495099.1:p.Gly1365=
ENST00000642728.1:n.405G=
ENST00000642797.1:c.4025G= ENSP00000493846.1:p.Gly1342=
ENST00000642936.1:c.4091G= ENSP00000494514.1:p.Gly1364=
ENST00000643088.1:c.4022G= ENSP00000494747.1:p.Gly1341=
ENST00000643177.1:n.237G=
ENST00000643426.1:n.1871G=
ENST00000643946.1:c.4154G= ENSP00000495927.1:p.Gly1385=
ENST00000644043.1:c.4094G= ENSP00000496262.1:p.Gly1365=
ENST00000644329.1:c.4022G= ENSP00000496611.1:p.Gly1341=
ENST00000644335.1:c.4025G= ENSP00000496317.1:p.Gly1342=
ENST00000644399.1:c.4144G=
ENST00000645024.1:n.2307G=
ENST00000645186.1:c.466G=
ENST00000646388.1:c.4223G= ENSP00000495921.1:p.Gly1408=
ENST00000646634.1:n.3038G=
ENST00000646674.1:n.1475G=
ENST00000647042.1:n.1446G=
ENST00000647180.1:n.1336G=
ENST00000219476.7:c.4223G= ENSP00000219476.3:p.Gly1408=
ENST00000350773.8:c.4154G= ENSP00000344383.4:p.Gly1385=
ENST00000382538.10:c.3878G= ENSP00000371978.6:p.Gly1293=
ENST00000401874.6:c.4022G= ENSP00000384468.2:p.Gly1341=
ENST00000439117.6:c.*3390G= ENSP00000406980.2:n.*3390G=
ENST00000439673.6:c.3914G= ENSP00000399232.2:p.Gly1305=
ENST00000497886.5:n.1981G=
ENST00000568454.5:c.4055G= ENSP00000454487.1:p.Gly1352=
ENST00000569110.1:c.405G=
ENST00000569930.1:n.1338G=
NM_000548.3:c.4223G= , LRG_487t1:c.4223G= NP_000539.2:p.Gly1408=
NM_001077183.1:c.4022G= NP_001070651.1:p.Gly1341=
NM_001114382.1:c.4154G= NP_001107854.1:p.Gly1385=
XM_005255529.3:c.4094G= XP_005255586.2:p.Gly1365=
XM_005255531.3:c.4025G= XP_005255588.2:p.Gly1342=
XM_011522636.1:c.4277G= XP_011520938.1:p.Gly1426=
XM_011522637.1:c.4274G= XP_011520939.1:p.Gly1425=
XM_011522638.1:c.4166G= XP_011520940.1:p.Gly1389=
XM_011522639.1:c.4148G= XP_011520941.1:p.Gly1383=
XM_011522640.1:c.4145G= XP_011520942.1:p.Gly1382=
XM_011522641.1:c.3914G= XP_011520943.1:p.Gly1305=
NM_000548.4:c.4223G= NP_000539.2:p.Gly1408=
NM_001077183.2:c.4022G= NP_001070651.1:p.Gly1341=
NM_001114382.2:c.4154G= NP_001107854.1:p.Gly1385=
NM_001318827.1:c.3914G= NP_001305756.1:p.Gly1305=
NM_001318829.1:c.3878G= NP_001305758.1:p.Gly1293=
NM_001318831.1:c.3491G= NP_001305760.1:p.Gly1164=
NM_001318832.1:c.4055G= NP_001305761.1:p.Gly1352=
NM_001363528.1:c.4025G= NP_001350457.1:p.Gly1342=
NM_021055.2:c.4094G= NP_066399.2:p.Gly1365=
XM_005255531.4:c.4025G= XP_005255588.2:p.Gly1342=
XM_011522636.2:c.4277G= XP_011520938.1:p.Gly1426=
XM_011522637.2:c.4274G= XP_011520939.1:p.Gly1425=
XM_011522638.2:c.4439G= XP_011520940.2:p.Gly1480=
XM_011522639.2:c.4148G= XP_011520941.1:p.Gly1383=
XM_011522640.2:c.4145G= XP_011520942.1:p.Gly1382=
XM_017023615.1:c.4220G= XP_016879104.1:p.Gly1407=
XM_017023616.1:c.4091G= XP_016879105.1:p.Gly1364=
XM_017023617.1:c.4187G= XP_016879106.1:p.Gly1396=
XM_017023618.1:c.2933G= XP_016879107.1:p.Gly978=
XM_024450413.1:c.4022G= XP_024306181.1:p.Gly1341=
NM_000548.5:c.4223G= MANE Select NP_000539.2:p.Gly1408=
NM_001370404.1:c.4091G= NP_001357333.1:p.Gly1364=
NM_001370405.1:c.4094G= NP_001357334.1:p.Gly1365=
NM_001077183.3:c.4022G= NP_001070651.1:p.Gly1341=
NM_001114382.3:c.4154G= NP_001107854.1:p.Gly1385=
NM_001318827.2:c.3914G= NP_001305756.1:p.Gly1305=
NM_001318829.2:c.3878G= NP_001305758.1:p.Gly1293=
NM_001318831.2:c.3491G= NP_001305760.1:p.Gly1164=
NM_001318832.2:c.4055G= NP_001305761.1:p.Gly1352=
NM_001363528.2:c.4025G= NP_001350457.1:p.Gly1342=
NM_021055.3:c.4094G= NP_066399.2:p.Gly1365=