Canonical Allele Identifier: CA394304523
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2090623795
gnomAD v3: 16-2085255-A-G
gnomAD v4: 16-2085255-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085255A>G , CM000678.2:g.2085255A>G GRCh38
NC_000016.9:g.2135256A>G , CM000678.1:g.2135256A>G GRCh37
NC_000016.8:g.2075257A>G NCBI36
NG_005895.1:g.40950A>G , LRG_487:g.40950A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2944A>G ENSP00000455997.2:n.*2944A>G
ENST00000642206.2:c.4442A>G ENSP00000495146.2:p.Gln1481Arg
ENST00000642365.2:c.4592A>G ENSP00000495459.2:p.Gln1531Arg
ENST00000644417.2:c.*4975A>G ENSP00000493912.2:n.*4975A>G
ENST00000646464.2:c.*7344A>G ENSP00000496610.2:n.*7344A>G
ENST00000219476.9:c.4595A>G MANE Select ENSP00000219476.3:p.Gln1532Arg
ENST00000350773.9:c.4526A>G ENSP00000344383.4:p.Gln1509Arg
ENST00000401874.7:c.4394A>G ENSP00000384468.2:p.Gln1465Arg
ENST00000568454.6:c.4427A>G ENSP00000454487.1:p.Gln1476Arg
ENST00000569110.2:c.818A>G
ENST00000569930.2:n.2477A>G
ENST00000642365.1:c.3249A>G
ENST00000642561.1:c.4466A>G ENSP00000495099.1:p.Gln1489Arg
ENST00000642728.1:n.777A>G
ENST00000642791.1:n.192A>G
ENST00000642797.1:c.4397A>G ENSP00000493846.1:p.Gln1466Arg
ENST00000642936.1:c.4463A>G ENSP00000494514.1:p.Gln1488Arg
ENST00000643088.1:c.4388A>G ENSP00000494747.1:p.Gln1463Arg
ENST00000643177.1:n.609A>G
ENST00000643426.1:n.2243A>G
ENST00000643946.1:c.4520A>G ENSP00000495927.1:p.Gln1507Arg
ENST00000644043.1:c.4466A>G ENSP00000496262.1:p.Gln1489Arg
ENST00000644278.1:n.77A>G
ENST00000644329.1:c.4394A>G ENSP00000496611.1:p.Gln1465Arg
ENST00000644335.1:c.4391A>G ENSP00000496317.1:p.Gln1464Arg
ENST00000644399.1:c.4516A>G
ENST00000645024.1:n.2679A>G
ENST00000646388.1:c.4589A>G ENSP00000495921.1:p.Gln1530Arg
ENST00000646634.1:n.3410A>G
ENST00000646674.1:n.1847A>G
ENST00000647042.1:n.1818A>G
ENST00000647180.1:n.1708A>G
ENST00000219476.7:c.4595A>G ENSP00000219476.3:p.Gln1532Arg
ENST00000350773.8:c.4526A>G ENSP00000344383.4:p.Gln1509Arg
ENST00000382538.10:c.4250A>G ENSP00000371978.6:p.Gln1417Arg
ENST00000401874.6:c.4394A>G ENSP00000384468.2:p.Gln1465Arg
ENST00000439117.6:c.*3762A>G ENSP00000406980.2:n.*3762A>G
ENST00000439673.6:c.4286A>G ENSP00000399232.2:p.Gln1429Arg
ENST00000497886.5:n.2353A>G
ENST00000568454.5:c.4427A>G ENSP00000454487.1:p.Gln1476Arg
ENST00000569110.1:c.777A>G
ENST00000569930.1:n.1710A>G
NM_000548.3:c.4595A>G , LRG_487t1:c.4595A>G NP_000539.2:p.Gln1532Arg
NM_001077183.1:c.4394A>G NP_001070651.1:p.Gln1465Arg
NM_001114382.1:c.4526A>G NP_001107854.1:p.Gln1509Arg
XM_005255529.3:c.4466A>G XP_005255586.2:p.Gln1489Arg
XM_005255531.3:c.4397A>G XP_005255588.2:p.Gln1466Arg
XM_011522636.1:c.4649A>G XP_011520938.1:p.Gln1550Arg
XM_011522637.1:c.4646A>G XP_011520939.1:p.Gln1549Arg
XM_011522638.1:c.4538A>G XP_011520940.1:p.Gln1513Arg
XM_011522639.1:c.4520A>G XP_011520941.1:p.Gln1507Arg
XM_011522640.1:c.4517A>G XP_011520942.1:p.Gln1506Arg
XM_011522641.1:c.4286A>G XP_011520943.1:p.Gln1429Arg
NM_000548.4:c.4595A>G NP_000539.2:p.Gln1532Arg
NM_001077183.2:c.4394A>G NP_001070651.1:p.Gln1465Arg
NM_001114382.2:c.4526A>G NP_001107854.1:p.Gln1509Arg
NM_001318827.1:c.4286A>G NP_001305756.1:p.Gln1429Arg
NM_001318829.1:c.4250A>G NP_001305758.1:p.Gln1417Arg
NM_001318831.1:c.3863A>G NP_001305760.1:p.Gln1288Arg
NM_001318832.1:c.4427A>G NP_001305761.1:p.Gln1476Arg
NM_001363528.1:c.4397A>G NP_001350457.1:p.Gln1466Arg
NM_021055.2:c.4466A>G NP_066399.2:p.Gln1489Arg
XM_005255531.4:c.4397A>G XP_005255588.2:p.Gln1466Arg
XM_011522636.2:c.4649A>G XP_011520938.1:p.Gln1550Arg
XM_011522637.2:c.4646A>G XP_011520939.1:p.Gln1549Arg
XM_011522638.2:c.4811A>G XP_011520940.2:p.Gln1604Arg
XM_011522639.2:c.4520A>G XP_011520941.1:p.Gln1507Arg
XM_011522640.2:c.4517A>G XP_011520942.1:p.Gln1506Arg
XM_017023615.1:c.4592A>G XP_016879104.1:p.Gln1531Arg
XM_017023616.1:c.4463A>G XP_016879105.1:p.Gln1488Arg
XM_017023617.1:c.4559A>G XP_016879106.1:p.Gln1520Arg
XM_017023618.1:c.3305A>G XP_016879107.1:p.Gln1102Arg
XM_024450413.1:c.4394A>G XP_024306181.1:p.Gln1465Arg
NM_000548.5:c.4595A>G MANE Select NP_000539.2:p.Gln1532Arg
NM_001370404.1:c.4463A>G NP_001357333.1:p.Gln1488Arg
NM_001370405.1:c.4466A>G NP_001357334.1:p.Gln1489Arg
NM_001077183.3:c.4394A>G NP_001070651.1:p.Gln1465Arg
NM_001114382.3:c.4526A>G NP_001107854.1:p.Gln1509Arg
NM_001318827.2:c.4286A>G NP_001305756.1:p.Gln1429Arg
NM_001318829.2:c.4250A>G NP_001305758.1:p.Gln1417Arg
NM_001318831.2:c.3863A>G NP_001305760.1:p.Gln1288Arg
NM_001318832.2:c.4427A>G NP_001305761.1:p.Gln1476Arg
NM_001363528.2:c.4397A>G NP_001350457.1:p.Gln1466Arg
NM_021055.3:c.4466A>G NP_066399.2:p.Gln1489Arg