Canonical Allele Identifier: CA2202019738
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085321A= , CM000678.2:g.2085321A= GRCh38
NC_000016.9:g.2135322A= , CM000678.1:g.2135322A= GRCh37
NC_000016.8:g.2075323A= NCBI36
NG_005895.1:g.41016A= , LRG_487:g.41016A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3010A= ENSP00000455997.2:n.*3010A=
ENST00000642206.2:c.4508A= ENSP00000495146.2:p.Gln1503=
ENST00000642365.2:c.4658A= ENSP00000495459.2:p.Gln1553=
ENST00000644417.2:c.*5041A= ENSP00000493912.2:n.*5041A=
ENST00000646464.2:c.*7410A= ENSP00000496610.2:n.*7410A=
ENST00000219476.9:c.4661A= MANE Select ENSP00000219476.3:p.Gln1554=
ENST00000350773.9:c.4592A= ENSP00000344383.4:p.Gln1531=
ENST00000401874.7:c.4460A= ENSP00000384468.2:p.Gln1487=
ENST00000568454.6:c.4493A= ENSP00000454487.1:p.Gln1498=
ENST00000569110.2:c.884A=
ENST00000569930.2:n.2543A=
ENST00000642365.1:c.3315A=
ENST00000642561.1:c.4532A= ENSP00000495099.1:p.Gln1511=
ENST00000642728.1:n.843A=
ENST00000642791.1:n.258A=
ENST00000642797.1:c.4463A= ENSP00000493846.1:p.Gln1488=
ENST00000642936.1:c.4529A= ENSP00000494514.1:p.Gln1510=
ENST00000643088.1:c.4454A= ENSP00000494747.1:p.Gln1485=
ENST00000643177.1:n.675A=
ENST00000643426.1:n.2309A=
ENST00000643946.1:c.4586A= ENSP00000495927.1:p.Gln1529=
ENST00000644043.1:c.4532A= ENSP00000496262.1:p.Gln1511=
ENST00000644278.1:n.143A=
ENST00000644329.1:c.4460A= ENSP00000496611.1:p.Gln1487=
ENST00000644335.1:c.4457A= ENSP00000496317.1:p.Gln1486=
ENST00000644399.1:c.4582A=
ENST00000645024.1:n.2745A=
ENST00000646388.1:c.4655A= ENSP00000495921.1:p.Gln1552=
ENST00000646634.1:n.3476A=
ENST00000646674.1:n.1913A=
ENST00000647042.1:n.1884A=
ENST00000647180.1:n.1774A=
ENST00000219476.7:c.4661A= ENSP00000219476.3:p.Gln1554=
ENST00000350773.8:c.4592A= ENSP00000344383.4:p.Gln1531=
ENST00000382538.10:c.4316A= ENSP00000371978.6:p.Gln1439=
ENST00000401874.6:c.4460A= ENSP00000384468.2:p.Gln1487=
ENST00000439117.6:c.*3828A= ENSP00000406980.2:n.*3828A=
ENST00000439673.6:c.4352A= ENSP00000399232.2:p.Gln1451=
ENST00000497886.5:n.2419A=
ENST00000568454.5:c.4493A= ENSP00000454487.1:p.Gln1498=
ENST00000569110.1:c.843A=
ENST00000569930.1:n.1776A=
NM_000548.3:c.4661A= , LRG_487t1:c.4661A= NP_000539.2:p.Gln1554=
NM_001077183.1:c.4460A= NP_001070651.1:p.Gln1487=
NM_001114382.1:c.4592A= NP_001107854.1:p.Gln1531=
XM_005255529.3:c.4532A= XP_005255586.2:p.Gln1511=
XM_005255531.3:c.4463A= XP_005255588.2:p.Gln1488=
XM_011522636.1:c.4715A= XP_011520938.1:p.Gln1572=
XM_011522637.1:c.4712A= XP_011520939.1:p.Gln1571=
XM_011522638.1:c.4604A= XP_011520940.1:p.Gln1535=
XM_011522639.1:c.4586A= XP_011520941.1:p.Gln1529=
XM_011522640.1:c.4583A= XP_011520942.1:p.Gln1528=
XM_011522641.1:c.4352A= XP_011520943.1:p.Gln1451=
NM_000548.4:c.4661A= NP_000539.2:p.Gln1554=
NM_001077183.2:c.4460A= NP_001070651.1:p.Gln1487=
NM_001114382.2:c.4592A= NP_001107854.1:p.Gln1531=
NM_001318827.1:c.4352A= NP_001305756.1:p.Gln1451=
NM_001318829.1:c.4316A= NP_001305758.1:p.Gln1439=
NM_001318831.1:c.3929A= NP_001305760.1:p.Gln1310=
NM_001318832.1:c.4493A= NP_001305761.1:p.Gln1498=
NM_001363528.1:c.4463A= NP_001350457.1:p.Gln1488=
NM_021055.2:c.4532A= NP_066399.2:p.Gln1511=
XM_005255531.4:c.4463A= XP_005255588.2:p.Gln1488=
XM_011522636.2:c.4715A= XP_011520938.1:p.Gln1572=
XM_011522637.2:c.4712A= XP_011520939.1:p.Gln1571=
XM_011522638.2:c.4877A= XP_011520940.2:p.Gln1626=
XM_011522639.2:c.4586A= XP_011520941.1:p.Gln1529=
XM_011522640.2:c.4583A= XP_011520942.1:p.Gln1528=
XM_017023615.1:c.4658A= XP_016879104.1:p.Gln1553=
XM_017023616.1:c.4529A= XP_016879105.1:p.Gln1510=
XM_017023617.1:c.4625A= XP_016879106.1:p.Gln1542=
XM_017023618.1:c.3371A= XP_016879107.1:p.Gln1124=
XM_024450413.1:c.4460A= XP_024306181.1:p.Gln1487=
NM_000548.5:c.4661A= MANE Select NP_000539.2:p.Gln1554=
NM_001370404.1:c.4529A= NP_001357333.1:p.Gln1510=
NM_001370405.1:c.4532A= NP_001357334.1:p.Gln1511=
NM_001077183.3:c.4460A= NP_001070651.1:p.Gln1487=
NM_001114382.3:c.4592A= NP_001107854.1:p.Gln1531=
NM_001318827.2:c.4352A= NP_001305756.1:p.Gln1451=
NM_001318829.2:c.4316A= NP_001305758.1:p.Gln1439=
NM_001318831.2:c.3929A= NP_001305760.1:p.Gln1310=
NM_001318832.2:c.4493A= NP_001305761.1:p.Gln1498=
NM_001363528.2:c.4463A= NP_001350457.1:p.Gln1488=
NM_021055.3:c.4532A= NP_066399.2:p.Gln1511=