Canonical Allele Identifier: CA973770606
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088253del , CM000678.2:g.2088253del GRCh38
NC_000016.9:g.2138254del , CM000678.1:g.2138254del GRCh37
NC_000016.8:g.2078255del NCBI36
NG_005895.1:g.43948del , LRG_487:g.43948del
NG_008617.1:g.54968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3536del ENSP00000455997.2:n.*3536del
ENST00000642206.2:c.5034del ENSP00000495146.2:p.Ser1679ProfsTer?
ENST00000642365.2:c.5184del ENSP00000495459.2:p.Ser1729ProfsTer?
ENST00000644417.2:c.*5700del ENSP00000493912.2:n.*5700del
ENST00000646464.2:c.*7936del ENSP00000496610.2:n.*7936del
ENST00000219476.9:c.5187del MANE Select ENSP00000219476.3:p.Ser1730ProfsTer?
ENST00000350773.9:c.5118del ENSP00000344383.4:p.Ser1707ProfsTer?
ENST00000401874.7:c.4986del ENSP00000384468.2:p.Ser1663ProfsTer?
ENST00000568454.6:c.5019del ENSP00000454487.1:p.Ser1674ProfsTer?
ENST00000569110.2:c.1410del
ENST00000569930.2:n.3069del
ENST00000642365.1:c.3841del
ENST00000642561.1:c.5046del ENSP00000495099.1:p.Ser1683ProfsTer?
ENST00000642791.1:n.784del
ENST00000642797.1:c.4989del ENSP00000493846.1:p.Ser1664ProfsTer?
ENST00000642936.1:c.5055del ENSP00000494514.1:p.Ser1686ProfsTer?
ENST00000643088.1:c.4980del ENSP00000494747.1:p.Ser1661ProfsTer?
ENST00000643426.1:n.2835del
ENST00000643946.1:c.5112del ENSP00000495927.1:p.Ser1705ProfsTer?
ENST00000644043.1:c.5058del ENSP00000496262.1:p.Ser1687ProfsTer?
ENST00000644329.1:c.5073del ENSP00000496611.1:p.Ser1692ProfsTer?
ENST00000644335.1:c.4983del ENSP00000496317.1:p.Ser1662ProfsTer?
ENST00000644399.1:c.5108del
ENST00000645024.1:n.3271del
ENST00000646388.1:c.5181del ENSP00000495921.1:p.Ser1728ProfsTer?
ENST00000646634.1:n.4002del
ENST00000646674.1:n.2439del
ENST00000647042.1:n.2410del
ENST00000647180.1:n.2300del
ENST00000219476.7:c.5187del ENSP00000219476.3:p.Ser1730ProfsTer?
ENST00000350773.8:c.5118del ENSP00000344383.4:p.Ser1707ProfsTer?
ENST00000382538.10:c.4842del ENSP00000371978.6:p.Ser1615ProfsTer?
ENST00000401874.6:c.4986del ENSP00000384468.2:p.Ser1663ProfsTer?
ENST00000439117.6:c.*4354del ENSP00000406980.2:n.*4354del
ENST00000439673.6:c.4878del ENSP00000399232.2:p.Ser1627ProfsTer?
ENST00000497886.5:n.2910del
ENST00000568454.5:c.5019del ENSP00000454487.1:p.Ser1674ProfsTer?
ENST00000569110.1:c.1369del
ENST00000569930.1:n.2302del
NM_000548.3:c.5187del , LRG_487t1:c.5187del NP_000539.2:p.Ser1730ProfsTer?
NM_001077183.1:c.4986del NP_001070651.1:p.Ser1663ProfsTer?
NM_001114382.1:c.5118del NP_001107854.1:p.Ser1707ProfsTer?
XM_005255529.3:c.5058del XP_005255586.2:p.Ser1687ProfsTer?
XM_005255531.3:c.4989del XP_005255588.2:p.Ser1664ProfsTer?
XM_011522636.1:c.5241del XP_011520938.1:p.Ser1748ProfsTer?
XM_011522637.1:c.5238del XP_011520939.1:p.Ser1747ProfsTer?
XM_011522638.1:c.5130del XP_011520940.1:p.Ser1711ProfsTer?
XM_011522639.1:c.5112del XP_011520941.1:p.Ser1705ProfsTer?
XM_011522640.1:c.5109del XP_011520942.1:p.Ser1704ProfsTer?
XM_011522641.1:c.4878del XP_011520943.1:p.Ser1627ProfsTer?
NM_000548.4:c.5187del NP_000539.2:p.Ser1730ProfsTer?
NM_001077183.2:c.4986del NP_001070651.1:p.Ser1663ProfsTer?
NM_001114382.2:c.5118del NP_001107854.1:p.Ser1707ProfsTer?
NM_001318827.1:c.4878del NP_001305756.1:p.Ser1627ProfsTer?
NM_001318829.1:c.4842del NP_001305758.1:p.Ser1615ProfsTer?
NM_001318831.1:c.4455del NP_001305760.1:p.Ser1486ProfsTer?
NM_001318832.1:c.5019del NP_001305761.1:p.Ser1674ProfsTer?
NM_001363528.1:c.4989del NP_001350457.1:p.Ser1664ProfsTer?
NM_021055.2:c.5058del NP_066399.2:p.Ser1687ProfsTer?
XM_005255531.4:c.4989del XP_005255588.2:p.Ser1664ProfsTer?
XM_011522636.2:c.5241del XP_011520938.1:p.Ser1748ProfsTer?
XM_011522637.2:c.5238del XP_011520939.1:p.Ser1747ProfsTer?
XM_011522638.2:c.5403del XP_011520940.2:p.Ser1802ProfsTer?
XM_011522639.2:c.5112del XP_011520941.1:p.Ser1705ProfsTer?
XM_011522640.2:c.5109del XP_011520942.1:p.Ser1704ProfsTer?
XM_017023615.1:c.5184del XP_016879104.1:p.Ser1729ProfsTer?
XM_017023616.1:c.5055del XP_016879105.1:p.Ser1686ProfsTer?
XM_017023617.1:c.5151del XP_016879106.1:p.Ser1718ProfsTer?
XM_017023618.1:c.3897del XP_016879107.1:p.Ser1300ProfsTer?
XM_024450413.1:c.5073del XP_024306181.1:p.Ser1692ProfsTer?
NM_000548.5:c.5187del MANE Select NP_000539.2:p.Ser1730ProfsTer?
NM_001370404.1:c.5055del NP_001357333.1:p.Ser1686ProfsTer?
NM_001370405.1:c.5046del NP_001357334.1:p.Ser1683ProfsTer?
NM_001077183.3:c.4986del NP_001070651.1:p.Ser1663ProfsTer?
NM_001114382.3:c.5118del NP_001107854.1:p.Ser1707ProfsTer?
NM_001318827.2:c.4878del NP_001305756.1:p.Ser1627ProfsTer?
NM_001318829.2:c.4842del NP_001305758.1:p.Ser1615ProfsTer?
NM_001318831.2:c.4455del NP_001305760.1:p.Ser1486ProfsTer?
NM_001318832.2:c.5019del NP_001305761.1:p.Ser1674ProfsTer?
NM_001363528.2:c.4989del NP_001350457.1:p.Ser1664ProfsTer?
NM_021055.3:c.5058del NP_066399.2:p.Ser1687ProfsTer?