Canonical Allele Identifier: CA394314626
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151631966

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088305A>C , CM000678.2:g.2088305A>C GRCh38
NC_000016.9:g.2138306A>C , CM000678.1:g.2138306A>C GRCh37
NC_000016.8:g.2078307A>C NCBI36
NG_005895.1:g.44000A>C , LRG_487:g.44000A>C
NG_008617.1:g.54916T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3588A>C ENSP00000455997.2:n.*3588A>C
ENST00000642206.2:c.5086A>C ENSP00000495146.2:p.Ile1696Leu
ENST00000642365.2:c.5236A>C ENSP00000495459.2:p.Ile1746Leu
ENST00000644417.2:c.*5752A>C ENSP00000493912.2:n.*5752A>C
ENST00000646464.2:c.*7988A>C ENSP00000496610.2:n.*7988A>C
ENST00000219476.9:c.5239A>C MANE Select ENSP00000219476.3:p.Ile1747Leu
ENST00000350773.9:c.5170A>C ENSP00000344383.4:p.Ile1724Leu
ENST00000401874.7:c.5038A>C ENSP00000384468.2:p.Ile1680Leu
ENST00000568454.6:c.5071A>C ENSP00000454487.1:p.Ile1691Leu
ENST00000569110.2:c.1462A>C
ENST00000569930.2:n.3121A>C
ENST00000642365.1:c.3893A>C
ENST00000642561.1:c.5098A>C ENSP00000495099.1:p.Ile1700Leu
ENST00000642791.1:n.836A>C
ENST00000642797.1:c.5041A>C ENSP00000493846.1:p.Ile1681Leu
ENST00000642936.1:c.5107A>C ENSP00000494514.1:p.Ile1703Leu
ENST00000643088.1:c.5032A>C ENSP00000494747.1:p.Ile1678Leu
ENST00000643426.1:n.2887A>C
ENST00000643946.1:c.5164A>C ENSP00000495927.1:p.Ile1722Leu
ENST00000644043.1:c.5110A>C ENSP00000496262.1:p.Ile1704Leu
ENST00000644329.1:c.5125A>C ENSP00000496611.1:p.Ile1709Leu
ENST00000644335.1:c.5035A>C ENSP00000496317.1:p.Ile1679Leu
ENST00000644399.1:c.5160A>C
ENST00000645024.1:n.3323A>C
ENST00000646388.1:c.5233A>C ENSP00000495921.1:p.Ile1745Leu
ENST00000646634.1:n.4054A>C
ENST00000646674.1:n.2491A>C
ENST00000647042.1:n.2462A>C
ENST00000647180.1:n.2352A>C
ENST00000219476.7:c.5239A>C ENSP00000219476.3:p.Ile1747Leu
ENST00000350773.8:c.5170A>C ENSP00000344383.4:p.Ile1724Leu
ENST00000382538.10:c.4894A>C ENSP00000371978.6:p.Ile1632Leu
ENST00000401874.6:c.5038A>C ENSP00000384468.2:p.Ile1680Leu
ENST00000439117.6:c.*4406A>C ENSP00000406980.2:n.*4406A>C
ENST00000439673.6:c.4930A>C ENSP00000399232.2:p.Ile1644Leu
ENST00000497886.5:n.2962A>C
ENST00000568454.5:c.5071A>C ENSP00000454487.1:p.Ile1691Leu
ENST00000569110.1:c.1421A>C
ENST00000569930.1:n.2354A>C
NM_000548.3:c.5239A>C , LRG_487t1:c.5239A>C NP_000539.2:p.Ile1747Leu
NM_001077183.1:c.5038A>C NP_001070651.1:p.Ile1680Leu
NM_001114382.1:c.5170A>C NP_001107854.1:p.Ile1724Leu
XM_005255529.3:c.5110A>C XP_005255586.2:p.Ile1704Leu
XM_005255531.3:c.5041A>C XP_005255588.2:p.Ile1681Leu
XM_011522636.1:c.5293A>C XP_011520938.1:p.Ile1765Leu
XM_011522637.1:c.5290A>C XP_011520939.1:p.Ile1764Leu
XM_011522638.1:c.5182A>C XP_011520940.1:p.Ile1728Leu
XM_011522639.1:c.5164A>C XP_011520941.1:p.Ile1722Leu
XM_011522640.1:c.5161A>C XP_011520942.1:p.Ile1721Leu
XM_011522641.1:c.4930A>C XP_011520943.1:p.Ile1644Leu
NM_000548.4:c.5239A>C NP_000539.2:p.Ile1747Leu
NM_001077183.2:c.5038A>C NP_001070651.1:p.Ile1680Leu
NM_001114382.2:c.5170A>C NP_001107854.1:p.Ile1724Leu
NM_001318827.1:c.4930A>C NP_001305756.1:p.Ile1644Leu
NM_001318829.1:c.4894A>C NP_001305758.1:p.Ile1632Leu
NM_001318831.1:c.4507A>C NP_001305760.1:p.Ile1503Leu
NM_001318832.1:c.5071A>C NP_001305761.1:p.Ile1691Leu
NM_001363528.1:c.5041A>C NP_001350457.1:p.Ile1681Leu
NM_021055.2:c.5110A>C NP_066399.2:p.Ile1704Leu
XM_005255531.4:c.5041A>C XP_005255588.2:p.Ile1681Leu
XM_011522636.2:c.5293A>C XP_011520938.1:p.Ile1765Leu
XM_011522637.2:c.5290A>C XP_011520939.1:p.Ile1764Leu
XM_011522638.2:c.5455A>C XP_011520940.2:p.Ile1819Leu
XM_011522639.2:c.5164A>C XP_011520941.1:p.Ile1722Leu
XM_011522640.2:c.5161A>C XP_011520942.1:p.Ile1721Leu
XM_017023615.1:c.5236A>C XP_016879104.1:p.Ile1746Leu
XM_017023616.1:c.5107A>C XP_016879105.1:p.Ile1703Leu
XM_017023617.1:c.5203A>C XP_016879106.1:p.Ile1735Leu
XM_017023618.1:c.3949A>C XP_016879107.1:p.Ile1317Leu
XM_024450413.1:c.5125A>C XP_024306181.1:p.Ile1709Leu
NM_000548.5:c.5239A>C MANE Select NP_000539.2:p.Ile1747Leu
NM_001370404.1:c.5107A>C NP_001357333.1:p.Ile1703Leu
NM_001370405.1:c.5098A>C NP_001357334.1:p.Ile1700Leu
NM_001077183.3:c.5038A>C NP_001070651.1:p.Ile1680Leu
NM_001114382.3:c.5170A>C NP_001107854.1:p.Ile1724Leu
NM_001318827.2:c.4930A>C NP_001305756.1:p.Ile1644Leu
NM_001318829.2:c.4894A>C NP_001305758.1:p.Ile1632Leu
NM_001318831.2:c.4507A>C NP_001305760.1:p.Ile1503Leu
NM_001318832.2:c.5071A>C NP_001305761.1:p.Ile1691Leu
NM_001363528.2:c.5041A>C NP_001350457.1:p.Ile1681Leu
NM_021055.3:c.5110A>C NP_066399.2:p.Ile1704Leu