Canonical Allele Identifier: CA394304577
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151551174

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085258T>C , CM000678.2:g.2085258T>C GRCh38
NC_000016.9:g.2135259T>C , CM000678.1:g.2135259T>C GRCh37
NC_000016.8:g.2075260T>C NCBI36
NG_005895.1:g.40953T>C , LRG_487:g.40953T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2947T>C ENSP00000455997.2:n.*2947T>C
ENST00000642206.2:c.4445T>C ENSP00000495146.2:p.Leu1482Pro
ENST00000642365.2:c.4595T>C ENSP00000495459.2:p.Leu1532Pro
ENST00000644417.2:c.*4978T>C ENSP00000493912.2:n.*4978T>C
ENST00000646464.2:c.*7347T>C ENSP00000496610.2:n.*7347T>C
ENST00000219476.9:c.4598T>C MANE Select ENSP00000219476.3:p.Leu1533Pro
ENST00000350773.9:c.4529T>C ENSP00000344383.4:p.Leu1510Pro
ENST00000401874.7:c.4397T>C ENSP00000384468.2:p.Leu1466Pro
ENST00000568454.6:c.4430T>C ENSP00000454487.1:p.Leu1477Pro
ENST00000569110.2:c.821T>C
ENST00000569930.2:n.2480T>C
ENST00000642365.1:c.3252T>C
ENST00000642561.1:c.4469T>C ENSP00000495099.1:p.Leu1490Pro
ENST00000642728.1:n.780T>C
ENST00000642791.1:n.195T>C
ENST00000642797.1:c.4400T>C ENSP00000493846.1:p.Leu1467Pro
ENST00000642936.1:c.4466T>C ENSP00000494514.1:p.Leu1489Pro
ENST00000643088.1:c.4391T>C ENSP00000494747.1:p.Leu1464Pro
ENST00000643177.1:n.612T>C
ENST00000643426.1:n.2246T>C
ENST00000643946.1:c.4523T>C ENSP00000495927.1:p.Leu1508Pro
ENST00000644043.1:c.4469T>C ENSP00000496262.1:p.Leu1490Pro
ENST00000644278.1:n.80T>C
ENST00000644329.1:c.4397T>C ENSP00000496611.1:p.Leu1466Pro
ENST00000644335.1:c.4394T>C ENSP00000496317.1:p.Leu1465Pro
ENST00000644399.1:c.4519T>C
ENST00000645024.1:n.2682T>C
ENST00000646388.1:c.4592T>C ENSP00000495921.1:p.Leu1531Pro
ENST00000646634.1:n.3413T>C
ENST00000646674.1:n.1850T>C
ENST00000647042.1:n.1821T>C
ENST00000647180.1:n.1711T>C
ENST00000219476.7:c.4598T>C ENSP00000219476.3:p.Leu1533Pro
ENST00000350773.8:c.4529T>C ENSP00000344383.4:p.Leu1510Pro
ENST00000382538.10:c.4253T>C ENSP00000371978.6:p.Leu1418Pro
ENST00000401874.6:c.4397T>C ENSP00000384468.2:p.Leu1466Pro
ENST00000439117.6:c.*3765T>C ENSP00000406980.2:n.*3765T>C
ENST00000439673.6:c.4289T>C ENSP00000399232.2:p.Leu1430Pro
ENST00000497886.5:n.2356T>C
ENST00000568454.5:c.4430T>C ENSP00000454487.1:p.Leu1477Pro
ENST00000569110.1:c.780T>C
ENST00000569930.1:n.1713T>C
NM_000548.3:c.4598T>C , LRG_487t1:c.4598T>C NP_000539.2:p.Leu1533Pro
NM_001077183.1:c.4397T>C NP_001070651.1:p.Leu1466Pro
NM_001114382.1:c.4529T>C NP_001107854.1:p.Leu1510Pro
XM_005255529.3:c.4469T>C XP_005255586.2:p.Leu1490Pro
XM_005255531.3:c.4400T>C XP_005255588.2:p.Leu1467Pro
XM_011522636.1:c.4652T>C XP_011520938.1:p.Leu1551Pro
XM_011522637.1:c.4649T>C XP_011520939.1:p.Leu1550Pro
XM_011522638.1:c.4541T>C XP_011520940.1:p.Leu1514Pro
XM_011522639.1:c.4523T>C XP_011520941.1:p.Leu1508Pro
XM_011522640.1:c.4520T>C XP_011520942.1:p.Leu1507Pro
XM_011522641.1:c.4289T>C XP_011520943.1:p.Leu1430Pro
NM_000548.4:c.4598T>C NP_000539.2:p.Leu1533Pro
NM_001077183.2:c.4397T>C NP_001070651.1:p.Leu1466Pro
NM_001114382.2:c.4529T>C NP_001107854.1:p.Leu1510Pro
NM_001318827.1:c.4289T>C NP_001305756.1:p.Leu1430Pro
NM_001318829.1:c.4253T>C NP_001305758.1:p.Leu1418Pro
NM_001318831.1:c.3866T>C NP_001305760.1:p.Leu1289Pro
NM_001318832.1:c.4430T>C NP_001305761.1:p.Leu1477Pro
NM_001363528.1:c.4400T>C NP_001350457.1:p.Leu1467Pro
NM_021055.2:c.4469T>C NP_066399.2:p.Leu1490Pro
XM_005255531.4:c.4400T>C XP_005255588.2:p.Leu1467Pro
XM_011522636.2:c.4652T>C XP_011520938.1:p.Leu1551Pro
XM_011522637.2:c.4649T>C XP_011520939.1:p.Leu1550Pro
XM_011522638.2:c.4814T>C XP_011520940.2:p.Leu1605Pro
XM_011522639.2:c.4523T>C XP_011520941.1:p.Leu1508Pro
XM_011522640.2:c.4520T>C XP_011520942.1:p.Leu1507Pro
XM_017023615.1:c.4595T>C XP_016879104.1:p.Leu1532Pro
XM_017023616.1:c.4466T>C XP_016879105.1:p.Leu1489Pro
XM_017023617.1:c.4562T>C XP_016879106.1:p.Leu1521Pro
XM_017023618.1:c.3308T>C XP_016879107.1:p.Leu1103Pro
XM_024450413.1:c.4397T>C XP_024306181.1:p.Leu1466Pro
NM_000548.5:c.4598T>C MANE Select NP_000539.2:p.Leu1533Pro
NM_001370404.1:c.4466T>C NP_001357333.1:p.Leu1489Pro
NM_001370405.1:c.4469T>C NP_001357334.1:p.Leu1490Pro
NM_001077183.3:c.4397T>C NP_001070651.1:p.Leu1466Pro
NM_001114382.3:c.4529T>C NP_001107854.1:p.Leu1510Pro
NM_001318827.2:c.4289T>C NP_001305756.1:p.Leu1430Pro
NM_001318829.2:c.4253T>C NP_001305758.1:p.Leu1418Pro
NM_001318831.2:c.3866T>C NP_001305760.1:p.Leu1289Pro
NM_001318832.2:c.4430T>C NP_001305761.1:p.Leu1477Pro
NM_001363528.2:c.4400T>C NP_001350457.1:p.Leu1467Pro
NM_021055.3:c.4469T>C NP_066399.2:p.Leu1490Pro