Canonical Allele Identifier: CA645594272
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2071784_2071867del , CM000678.2:g.2071784_2071867del GRCh38
NC_000016.9:g.2121785_2121868del , CM000678.1:g.2121785_2121868del GRCh37
NC_000016.8:g.2061786_2061869del NCBI36
NG_005895.1:g.27479_27562del , LRG_487:g.27479_27562del

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*494_*577del ENSP00000455997.2:n.*494_*577del
ENST00000642206.2:c.1992_2075del ENSP00000495146.2:p.Met664_Pro692delinsIl...
ENST00000642365.2:c.1947_2030del ENSP00000495459.2:p.Met649_Pro677delinsIl...
ENST00000644417.2:c.*1384_*1467del ENSP00000493912.2:n.*1384_*1467del
ENST00000646464.2:c.*1552_*1635del ENSP00000496610.2:n.*1552_*1635del
ENST00000219476.9:c.1947_2030del MANE Select ENSP00000219476.3:p.Met649_Pro677delinsIl...
ENST00000350773.9:c.1947_2030del ENSP00000344383.4:p.Met649_Pro677delinsIl...
ENST00000401874.7:c.1947_2030del ENSP00000384468.2:p.Met649_Pro677delinsIl...
ENST00000563346.2:n.125_208del
ENST00000568454.6:c.1980_2063del ENSP00000454487.1:p.Met660_Pro688delinsIl...
ENST00000642365.1:c.604_687del
ENST00000642561.1:c.1947_2030del ENSP00000495099.1:p.Met649_Pro677delinsIl...
ENST00000642797.1:c.1947_2030del ENSP00000493846.1:p.Met649_Pro677delinsIl...
ENST00000642936.1:c.1947_2030del ENSP00000494514.1:p.Met649_Pro677delinsIl...
ENST00000643088.1:c.1947_2030del ENSP00000494747.1:p.Met649_Pro677delinsIl...
ENST00000643298.1:c.*1449_*1532del ENSP00000494393.1:n.*1449_*1532del
ENST00000643946.1:c.1947_2030del ENSP00000495927.1:p.Met649_Pro677delinsIl...
ENST00000644043.1:c.1947_2030del ENSP00000496262.1:p.Met649_Pro677delinsIl...
ENST00000644329.1:c.1947_2030del ENSP00000496611.1:p.Met649_Pro677delinsIl...
ENST00000644335.1:c.1947_2030del ENSP00000496317.1:p.Met649_Pro677delinsIl...
ENST00000644399.1:c.1940_2023del
ENST00000644847.1:n.939_1022del
ENST00000645024.1:n.229_312del
ENST00000645552.1:n.227_310del
ENST00000646388.1:c.1947_2030del ENSP00000495921.1:p.Met649_Pro677delinsIl...
ENST00000646634.1:n.960_1043del
ENST00000219476.7:c.1947_2030del ENSP00000219476.3:p.Met649_Pro677delinsIl...
ENST00000350773.8:c.1947_2030del ENSP00000344383.4:p.Met649_Pro677delinsIl...
ENST00000382538.10:c.1800_1883del ENSP00000371978.6:p.Met600_Pro628delinsIl...
ENST00000401874.6:c.1947_2030del ENSP00000384468.2:p.Met649_Pro677delinsIl...
ENST00000439117.6:c.*1246_*1329del ENSP00000406980.2:n.*1246_*1329del
ENST00000439673.6:c.1836_1919del ENSP00000399232.2:p.Met612_Pro640delinsIl...
ENST00000488675.5:n.454_537del
ENST00000563346.1:n.16_99del
ENST00000568454.5:c.1980_2063del ENSP00000454487.1:p.Met660_Pro688delinsIl...
NM_000548.3:c.1947_2030del , LRG_487t1:c.1947_2030del NP_000539.2:p.Met649_Pro677delinsIle
NM_001077183.1:c.1947_2030del NP_001070651.1:p.Met649_Pro677delinsIle
NM_001114382.1:c.1947_2030del NP_001107854.1:p.Met649_Pro677delinsIle
XM_005255529.3:c.1947_2030del XP_005255586.2:p.Met649_Pro677delinsIle
XM_005255531.3:c.1947_2030del XP_005255588.2:p.Met649_Pro677delinsIle
XM_011522636.1:c.1947_2030del XP_011520938.1:p.Met649_Pro677delinsIle
XM_011522637.1:c.1947_2030del XP_011520939.1:p.Met649_Pro677delinsIle
XM_011522638.1:c.1836_1919del XP_011520940.1:p.Met612_Pro640delinsIle
XM_011522639.1:c.1947_2030del XP_011520941.1:p.Met649_Pro677delinsIle
XM_011522640.1:c.1947_2030del XP_011520942.1:p.Met649_Pro677delinsIle
XM_011522641.1:c.1836_1919del XP_011520943.1:p.Met612_Pro640delinsIle
NM_000548.4:c.1947_2030del NP_000539.2:p.Met649_Pro677delinsIle
NM_001077183.2:c.1947_2030del NP_001070651.1:p.Met649_Pro677delinsIle
NM_001114382.2:c.1947_2030del NP_001107854.1:p.Met649_Pro677delinsIle
NM_001318827.1:c.1836_1919del NP_001305756.1:p.Met612_Pro640delinsIle
NM_001318829.1:c.1800_1883del NP_001305758.1:p.Met600_Pro628delinsIle
NM_001318831.1:c.1347_1430del NP_001305760.1:p.Met449_Pro477delinsIle
NM_001318832.1:c.1980_2063del NP_001305761.1:p.Met660_Pro688delinsIle
NM_001363528.1:c.1947_2030del NP_001350457.1:p.Met649_Pro677delinsIle
NM_021055.2:c.1947_2030del NP_066399.2:p.Met649_Pro677delinsIle
XM_005255531.4:c.1947_2030del XP_005255588.2:p.Met649_Pro677delinsIle
XM_011522636.2:c.1947_2030del XP_011520938.1:p.Met649_Pro677delinsIle
XM_011522637.2:c.1947_2030del XP_011520939.1:p.Met649_Pro677delinsIle
XM_011522638.2:c.2109_2192del XP_011520940.2:p.Met703_Pro731delinsIle
XM_011522639.2:c.1947_2030del XP_011520941.1:p.Met649_Pro677delinsIle
XM_011522640.2:c.1947_2030del XP_011520942.1:p.Met649_Pro677delinsIle
XM_017023615.1:c.1947_2030del XP_016879104.1:p.Met649_Pro677delinsIle
XM_017023616.1:c.1947_2030del XP_016879105.1:p.Met649_Pro677delinsIle
XM_017023617.1:c.2109_2192del XP_016879106.1:p.Met703_Pro731delinsIle
XM_017023618.1:c.603_686del XP_016879107.1:p.Met201_Pro229delinsIle
XM_024450413.1:c.1947_2030del XP_024306181.1:p.Met649_Pro677delinsIle
NM_000548.5:c.1947_2030del MANE Select NP_000539.2:p.Met649_Pro677delinsIle
NM_001370404.1:c.1947_2030del NP_001357333.1:p.Met649_Pro677delinsIle
NM_001370405.1:c.1947_2030del NP_001357334.1:p.Met649_Pro677delinsIle
NM_001077183.3:c.1947_2030del NP_001070651.1:p.Met649_Pro677delinsIle
NM_001114382.3:c.1947_2030del NP_001107854.1:p.Met649_Pro677delinsIle
NM_001318827.2:c.1836_1919del NP_001305756.1:p.Met612_Pro640delinsIle
NM_001318829.2:c.1800_1883del NP_001305758.1:p.Met600_Pro628delinsIle
NM_001318831.2:c.1347_1430del NP_001305760.1:p.Met449_Pro477delinsIle
NM_001318832.2:c.1980_2063del NP_001305761.1:p.Met660_Pro688delinsIle
NM_001363528.2:c.1947_2030del NP_001350457.1:p.Met649_Pro677delinsIle
NM_021055.3:c.1947_2030del NP_066399.2:p.Met649_Pro677delinsIle