Canonical Allele Identifier: CA017812
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49221
dbSNP Id: rs137854232

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2076088_2076089del , CM000678.2:g.2076088_2076089del GRCh38
NC_000016.9:g.2126089_2126090del , CM000678.1:g.2126089_2126090del GRCh37
NC_000016.8:g.2066090_2066091del NCBI36
NG_005895.1:g.31783_31784del , LRG_487:g.31783_31784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1207_*1208del ENSP00000455997.2:n.*1207_*1208del
ENST00000642206.2:c.2705_2706del ENSP00000495146.2:p.Cys902SerfsTer27
ENST00000642365.2:c.2660_2661del ENSP00000495459.2:p.Cys887SerfsTer27
ENST00000644417.2:c.*2097_*2098del ENSP00000493912.2:n.*2097_*2098del
ENST00000646464.2:c.*3714_*3715del ENSP00000496610.2:n.*3714_*3715del
ENST00000219476.9:c.2660_2661del MANE Select ENSP00000219476.3:p.Cys887SerfsTer27
ENST00000350773.9:c.2660_2661del ENSP00000344383.4:p.Cys887SerfsTer27
ENST00000401874.7:c.2660_2661del ENSP00000384468.2:p.Cys887SerfsTer27
ENST00000568454.6:c.2693_2694del ENSP00000454487.1:p.Cys898SerfsTer27
ENST00000642365.1:c.1317_1318del
ENST00000642561.1:c.2660_2661del ENSP00000495099.1:p.Cys887SerfsTer27
ENST00000642797.1:c.2660_2661del ENSP00000493846.1:p.Cys887SerfsTer27
ENST00000642936.1:c.2660_2661del ENSP00000494514.1:p.Cys887SerfsTer27
ENST00000643088.1:c.2660_2661del ENSP00000494747.1:p.Cys887SerfsTer27
ENST00000643298.1:c.*2162_*2163del ENSP00000494393.1:n.*2162_*2163del
ENST00000643946.1:c.2660_2661del ENSP00000495927.1:p.Cys887SerfsTer27
ENST00000644043.1:c.2660_2661del ENSP00000496262.1:p.Cys887SerfsTer27
ENST00000644329.1:c.2660_2661del ENSP00000496611.1:p.Cys887SerfsTer27
ENST00000644335.1:c.2660_2661del ENSP00000496317.1:p.Cys887SerfsTer27
ENST00000644399.1:c.2653_2654del
ENST00000645024.1:n.942_943del
ENST00000646388.1:c.2660_2661del ENSP00000495921.1:p.Cys887SerfsTer27
ENST00000646634.1:n.1673_1674del
ENST00000219476.7:c.2660_2661del ENSP00000219476.3:p.Cys887SerfsTer27
ENST00000350773.8:c.2660_2661del ENSP00000344383.4:p.Cys887SerfsTer27
ENST00000382538.10:c.2513_2514del ENSP00000371978.6:p.Cys838SerfsTer27
ENST00000401874.6:c.2660_2661del ENSP00000384468.2:p.Cys887SerfsTer27
ENST00000439117.6:c.*1959_*1960del ENSP00000406980.2:n.*1959_*1960del
ENST00000439673.6:c.2549_2550del ENSP00000399232.2:p.Cys850SerfsTer27
ENST00000568454.5:c.2693_2694del ENSP00000454487.1:p.Cys898SerfsTer27
NM_000548.3:c.2660_2661del , LRG_487t1:c.2660_2661del NP_000539.2:p.Cys887SerfsTer27
NM_001077183.1:c.2660_2661del NP_001070651.1:p.Cys887SerfsTer27
NM_001114382.1:c.2660_2661del NP_001107854.1:p.Cys887SerfsTer27
XM_005255529.3:c.2660_2661del XP_005255586.2:p.Cys887SerfsTer27
XM_005255531.3:c.2660_2661del XP_005255588.2:p.Cys887SerfsTer27
XM_011522636.1:c.2660_2661del XP_011520938.1:p.Cys887SerfsTer27
XM_011522637.1:c.2660_2661del XP_011520939.1:p.Cys887SerfsTer27
XM_011522638.1:c.2549_2550del XP_011520940.1:p.Cys850SerfsTer27
XM_011522639.1:c.2660_2661del XP_011520941.1:p.Cys887SerfsTer27
XM_011522640.1:c.2660_2661del XP_011520942.1:p.Cys887SerfsTer27
XM_011522641.1:c.2549_2550del XP_011520943.1:p.Cys850SerfsTer27
NM_000548.4:c.2660_2661del NP_000539.2:p.Cys887SerfsTer27
NM_001077183.2:c.2660_2661del NP_001070651.1:p.Cys887SerfsTer27
NM_001114382.2:c.2660_2661del NP_001107854.1:p.Cys887SerfsTer27
NM_001318827.1:c.2549_2550del NP_001305756.1:p.Cys850SerfsTer27
NM_001318829.1:c.2513_2514del NP_001305758.1:p.Cys838SerfsTer27
NM_001318831.1:c.2060_2061del NP_001305760.1:p.Cys687SerfsTer27
NM_001318832.1:c.2693_2694del NP_001305761.1:p.Cys898SerfsTer27
NM_001363528.1:c.2660_2661del NP_001350457.1:p.Cys887SerfsTer27
NM_021055.2:c.2660_2661del NP_066399.2:p.Cys887SerfsTer27
XM_005255531.4:c.2660_2661del XP_005255588.2:p.Cys887SerfsTer27
XM_011522636.2:c.2660_2661del XP_011520938.1:p.Cys887SerfsTer27
XM_011522637.2:c.2660_2661del XP_011520939.1:p.Cys887SerfsTer27
XM_011522638.2:c.2822_2823del XP_011520940.2:p.Cys941SerfsTer27
XM_011522639.2:c.2660_2661del XP_011520941.1:p.Cys887SerfsTer27
XM_011522640.2:c.2660_2661del XP_011520942.1:p.Cys887SerfsTer27
XM_017023615.1:c.2660_2661del XP_016879104.1:p.Cys887SerfsTer27
XM_017023616.1:c.2660_2661del XP_016879105.1:p.Cys887SerfsTer27
XM_017023617.1:c.2822_2823del XP_016879106.1:p.Cys941SerfsTer27
XM_017023618.1:c.1316_1317del XP_016879107.1:p.Cys439SerfsTer27
XM_024450413.1:c.2660_2661del XP_024306181.1:p.Cys887SerfsTer27
NM_000548.5:c.2660_2661del MANE Select NP_000539.2:p.Cys887SerfsTer27
NM_001370404.1:c.2660_2661del NP_001357333.1:p.Cys887SerfsTer27
NM_001370405.1:c.2660_2661del NP_001357334.1:p.Cys887SerfsTer27
NM_001077183.3:c.2660_2661del NP_001070651.1:p.Cys887SerfsTer27
NM_001114382.3:c.2660_2661del NP_001107854.1:p.Cys887SerfsTer27
NM_001318827.2:c.2549_2550del NP_001305756.1:p.Cys850SerfsTer27
NM_001318829.2:c.2513_2514del NP_001305758.1:p.Cys838SerfsTer27
NM_001318831.2:c.2060_2061del NP_001305760.1:p.Cys687SerfsTer27
NM_001318832.2:c.2693_2694del NP_001305761.1:p.Cys898SerfsTer27
NM_001363528.2:c.2660_2661del NP_001350457.1:p.Cys887SerfsTer27
NM_021055.3:c.2660_2661del NP_066399.2:p.Cys887SerfsTer27