Canonical Allele Identifier: CA394305076
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151553804

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085317G>C , CM000678.2:g.2085317G>C GRCh38
NC_000016.9:g.2135318G>C , CM000678.1:g.2135318G>C GRCh37
NC_000016.8:g.2075319G>C NCBI36
NG_005895.1:g.41012G>C , LRG_487:g.41012G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3006G>C ENSP00000455997.2:n.*3006G>C
ENST00000642206.2:c.4504G>C ENSP00000495146.2:p.Gly1502Arg
ENST00000642365.2:c.4654G>C ENSP00000495459.2:p.Gly1552Arg
ENST00000644417.2:c.*5037G>C ENSP00000493912.2:n.*5037G>C
ENST00000646464.2:c.*7406G>C ENSP00000496610.2:n.*7406G>C
ENST00000219476.9:c.4657G>C MANE Select ENSP00000219476.3:p.Gly1553Arg
ENST00000350773.9:c.4588G>C ENSP00000344383.4:p.Gly1530Arg
ENST00000401874.7:c.4456G>C ENSP00000384468.2:p.Gly1486Arg
ENST00000568454.6:c.4489G>C ENSP00000454487.1:p.Gly1497Arg
ENST00000569110.2:c.880G>C
ENST00000569930.2:n.2539G>C
ENST00000642365.1:c.3311G>C
ENST00000642561.1:c.4528G>C ENSP00000495099.1:p.Gly1510Arg
ENST00000642728.1:n.839G>C
ENST00000642791.1:n.254G>C
ENST00000642797.1:c.4459G>C ENSP00000493846.1:p.Gly1487Arg
ENST00000642936.1:c.4525G>C ENSP00000494514.1:p.Gly1509Arg
ENST00000643088.1:c.4450G>C ENSP00000494747.1:p.Gly1484Arg
ENST00000643177.1:n.671G>C
ENST00000643426.1:n.2305G>C
ENST00000643946.1:c.4582G>C ENSP00000495927.1:p.Gly1528Arg
ENST00000644043.1:c.4528G>C ENSP00000496262.1:p.Gly1510Arg
ENST00000644278.1:n.139G>C
ENST00000644329.1:c.4456G>C ENSP00000496611.1:p.Gly1486Arg
ENST00000644335.1:c.4453G>C ENSP00000496317.1:p.Gly1485Arg
ENST00000644399.1:c.4578G>C
ENST00000645024.1:n.2741G>C
ENST00000646388.1:c.4651G>C ENSP00000495921.1:p.Gly1551Arg
ENST00000646634.1:n.3472G>C
ENST00000646674.1:n.1909G>C
ENST00000647042.1:n.1880G>C
ENST00000647180.1:n.1770G>C
ENST00000219476.7:c.4657G>C ENSP00000219476.3:p.Gly1553Arg
ENST00000350773.8:c.4588G>C ENSP00000344383.4:p.Gly1530Arg
ENST00000382538.10:c.4312G>C ENSP00000371978.6:p.Gly1438Arg
ENST00000401874.6:c.4456G>C ENSP00000384468.2:p.Gly1486Arg
ENST00000439117.6:c.*3824G>C ENSP00000406980.2:n.*3824G>C
ENST00000439673.6:c.4348G>C ENSP00000399232.2:p.Gly1450Arg
ENST00000497886.5:n.2415G>C
ENST00000568454.5:c.4489G>C ENSP00000454487.1:p.Gly1497Arg
ENST00000569110.1:c.839G>C
ENST00000569930.1:n.1772G>C
NM_000548.3:c.4657G>C , LRG_487t1:c.4657G>C NP_000539.2:p.Gly1553Arg
NM_001077183.1:c.4456G>C NP_001070651.1:p.Gly1486Arg
NM_001114382.1:c.4588G>C NP_001107854.1:p.Gly1530Arg
XM_005255529.3:c.4528G>C XP_005255586.2:p.Gly1510Arg
XM_005255531.3:c.4459G>C XP_005255588.2:p.Gly1487Arg
XM_011522636.1:c.4711G>C XP_011520938.1:p.Gly1571Arg
XM_011522637.1:c.4708G>C XP_011520939.1:p.Gly1570Arg
XM_011522638.1:c.4600G>C XP_011520940.1:p.Gly1534Arg
XM_011522639.1:c.4582G>C XP_011520941.1:p.Gly1528Arg
XM_011522640.1:c.4579G>C XP_011520942.1:p.Gly1527Arg
XM_011522641.1:c.4348G>C XP_011520943.1:p.Gly1450Arg
NM_000548.4:c.4657G>C NP_000539.2:p.Gly1553Arg
NM_001077183.2:c.4456G>C NP_001070651.1:p.Gly1486Arg
NM_001114382.2:c.4588G>C NP_001107854.1:p.Gly1530Arg
NM_001318827.1:c.4348G>C NP_001305756.1:p.Gly1450Arg
NM_001318829.1:c.4312G>C NP_001305758.1:p.Gly1438Arg
NM_001318831.1:c.3925G>C NP_001305760.1:p.Gly1309Arg
NM_001318832.1:c.4489G>C NP_001305761.1:p.Gly1497Arg
NM_001363528.1:c.4459G>C NP_001350457.1:p.Gly1487Arg
NM_021055.2:c.4528G>C NP_066399.2:p.Gly1510Arg
XM_005255531.4:c.4459G>C XP_005255588.2:p.Gly1487Arg
XM_011522636.2:c.4711G>C XP_011520938.1:p.Gly1571Arg
XM_011522637.2:c.4708G>C XP_011520939.1:p.Gly1570Arg
XM_011522638.2:c.4873G>C XP_011520940.2:p.Gly1625Arg
XM_011522639.2:c.4582G>C XP_011520941.1:p.Gly1528Arg
XM_011522640.2:c.4579G>C XP_011520942.1:p.Gly1527Arg
XM_017023615.1:c.4654G>C XP_016879104.1:p.Gly1552Arg
XM_017023616.1:c.4525G>C XP_016879105.1:p.Gly1509Arg
XM_017023617.1:c.4621G>C XP_016879106.1:p.Gly1541Arg
XM_017023618.1:c.3367G>C XP_016879107.1:p.Gly1123Arg
XM_024450413.1:c.4456G>C XP_024306181.1:p.Gly1486Arg
NM_000548.5:c.4657G>C MANE Select NP_000539.2:p.Gly1553Arg
NM_001370404.1:c.4525G>C NP_001357333.1:p.Gly1509Arg
NM_001370405.1:c.4528G>C NP_001357334.1:p.Gly1510Arg
NM_001077183.3:c.4456G>C NP_001070651.1:p.Gly1486Arg
NM_001114382.3:c.4588G>C NP_001107854.1:p.Gly1530Arg
NM_001318827.2:c.4348G>C NP_001305756.1:p.Gly1450Arg
NM_001318829.2:c.4312G>C NP_001305758.1:p.Gly1438Arg
NM_001318831.2:c.3925G>C NP_001305760.1:p.Gly1309Arg
NM_001318832.2:c.4489G>C NP_001305761.1:p.Gly1497Arg
NM_001363528.2:c.4459G>C NP_001350457.1:p.Gly1487Arg
NM_021055.3:c.4528G>C NP_066399.2:p.Gly1510Arg