Canonical Allele Identifier: CA658798503
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523958
dbSNP Id: rs1555441221

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088475del , CM000678.2:g.2088475del GRCh38
NC_000016.9:g.2138476del , CM000678.1:g.2138476del GRCh37
NC_000016.8:g.2078477del NCBI36
NG_005895.1:g.44170del , LRG_487:g.44170del
NG_008617.1:g.54749del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3638del ENSP00000455997.2:n.*3638del
ENST00000642206.2:c.5136del ENSP00000495146.2:p.Ser1713AlafsTer?
ENST00000642365.2:c.5286del ENSP00000495459.2:p.Ser1763AlafsTer?
ENST00000644417.2:c.*5802del ENSP00000493912.2:n.*5802del
ENST00000646464.2:c.*8038del ENSP00000496610.2:n.*8038del
ENST00000219476.9:c.5289del MANE Select ENSP00000219476.3:p.Ser1764AlafsTer?
ENST00000350773.9:c.5220del ENSP00000344383.4:p.Ser1741AlafsTer?
ENST00000401874.7:c.5088del ENSP00000384468.2:p.Ser1697AlafsTer?
ENST00000568454.6:c.5121del ENSP00000454487.1:p.Ser1708AlafsTer?
ENST00000569110.2:c.1512del
ENST00000569930.2:n.3171del
ENST00000642365.1:c.3943del
ENST00000642561.1:c.5148del ENSP00000495099.1:p.Ser1717AlafsTer?
ENST00000642791.1:n.886del
ENST00000642797.1:c.5091del ENSP00000493846.1:p.Ser1698AlafsTer?
ENST00000642936.1:c.5157del ENSP00000494514.1:p.Ser1720AlafsTer?
ENST00000643088.1:c.5082del ENSP00000494747.1:p.Ser1695AlafsTer?
ENST00000643426.1:n.2937del
ENST00000643946.1:c.5214del ENSP00000495927.1:p.Ser1739AlafsTer?
ENST00000644043.1:c.5160del ENSP00000496262.1:p.Ser1721AlafsTer?
ENST00000644329.1:c.5175del ENSP00000496611.1:p.Ser1726AlafsTer?
ENST00000644335.1:c.5085del ENSP00000496317.1:p.Ser1696AlafsTer?
ENST00000644399.1:c.5210del
ENST00000645024.1:n.3373del
ENST00000646388.1:c.5283del ENSP00000495921.1:p.Ser1762AlafsTer?
ENST00000646634.1:n.4104del
ENST00000646674.1:n.2541del
ENST00000647042.1:n.2512del
ENST00000647180.1:n.2402del
ENST00000219476.7:c.5289del ENSP00000219476.3:p.Ser1764AlafsTer?
ENST00000350773.8:c.5220del ENSP00000344383.4:p.Ser1741AlafsTer?
ENST00000382538.10:c.4944del ENSP00000371978.6:p.Ser1649AlafsTer?
ENST00000401874.6:c.5088del ENSP00000384468.2:p.Ser1697AlafsTer?
ENST00000439117.6:c.*4456del ENSP00000406980.2:n.*4456del
ENST00000439673.6:c.4980del ENSP00000399232.2:p.Ser1661AlafsTer?
ENST00000497886.5:n.3012del
ENST00000568454.5:c.5121del ENSP00000454487.1:p.Ser1708AlafsTer?
ENST00000569110.1:c.1471del
ENST00000569930.1:n.2404del
NM_000548.3:c.5289del , LRG_487t1:c.5289del NP_000539.2:p.Ser1764AlafsTer?
NM_001077183.1:c.5088del NP_001070651.1:p.Ser1697AlafsTer?
NM_001114382.1:c.5220del NP_001107854.1:p.Ser1741AlafsTer?
XM_005255529.3:c.5160del XP_005255586.2:p.Ser1721AlafsTer?
XM_005255531.3:c.5091del XP_005255588.2:p.Ser1698AlafsTer?
XM_011522636.1:c.5343del XP_011520938.1:p.Ser1782AlafsTer?
XM_011522637.1:c.5340del XP_011520939.1:p.Ser1781AlafsTer?
XM_011522638.1:c.5232del XP_011520940.1:p.Ser1745AlafsTer?
XM_011522639.1:c.5214del XP_011520941.1:p.Ser1739AlafsTer?
XM_011522640.1:c.5211del XP_011520942.1:p.Ser1738AlafsTer?
XM_011522641.1:c.4980del XP_011520943.1:p.Ser1661AlafsTer?
NM_000548.4:c.5289del NP_000539.2:p.Ser1764AlafsTer?
NM_001077183.2:c.5088del NP_001070651.1:p.Ser1697AlafsTer?
NM_001114382.2:c.5220del NP_001107854.1:p.Ser1741AlafsTer?
NM_001318827.1:c.4980del NP_001305756.1:p.Ser1661AlafsTer?
NM_001318829.1:c.4944del NP_001305758.1:p.Ser1649AlafsTer?
NM_001318831.1:c.4557del NP_001305760.1:p.Ser1520AlafsTer?
NM_001318832.1:c.5121del NP_001305761.1:p.Ser1708AlafsTer?
NM_001363528.1:c.5091del NP_001350457.1:p.Ser1698AlafsTer?
NM_021055.2:c.5160del NP_066399.2:p.Ser1721AlafsTer?
XM_005255531.4:c.5091del XP_005255588.2:p.Ser1698AlafsTer?
XM_011522636.2:c.5343del XP_011520938.1:p.Ser1782AlafsTer?
XM_011522637.2:c.5340del XP_011520939.1:p.Ser1781AlafsTer?
XM_011522638.2:c.5505del XP_011520940.2:p.Ser1836AlafsTer?
XM_011522639.2:c.5214del XP_011520941.1:p.Ser1739AlafsTer?
XM_011522640.2:c.5211del XP_011520942.1:p.Ser1738AlafsTer?
XM_017023615.1:c.5286del XP_016879104.1:p.Ser1763AlafsTer?
XM_017023616.1:c.5157del XP_016879105.1:p.Ser1720AlafsTer?
XM_017023617.1:c.5253del XP_016879106.1:p.Ser1752AlafsTer?
XM_017023618.1:c.3999del XP_016879107.1:p.Ser1334AlafsTer?
XM_024450413.1:c.5175del XP_024306181.1:p.Ser1726AlafsTer?
NM_000548.5:c.5289del MANE Select NP_000539.2:p.Ser1764AlafsTer?
NM_001370404.1:c.5157del NP_001357333.1:p.Ser1720AlafsTer?
NM_001370405.1:c.5148del NP_001357334.1:p.Ser1717AlafsTer?
NM_001077183.3:c.5088del NP_001070651.1:p.Ser1697AlafsTer?
NM_001114382.3:c.5220del NP_001107854.1:p.Ser1741AlafsTer?
NM_001318827.2:c.4980del NP_001305756.1:p.Ser1661AlafsTer?
NM_001318829.2:c.4944del NP_001305758.1:p.Ser1649AlafsTer?
NM_001318831.2:c.4557del NP_001305760.1:p.Ser1520AlafsTer?
NM_001318832.2:c.5121del NP_001305761.1:p.Ser1708AlafsTer?
NM_001363528.2:c.5091del NP_001350457.1:p.Ser1698AlafsTer?
NM_021055.3:c.5160del NP_066399.2:p.Ser1721AlafsTer?