Canonical Allele Identifier: CA020685
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49531
dbSNP Id: rs137854040

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085209_2085219dup , CM000678.2:g.2085209_2085219dup GRCh38
NC_000016.9:g.2135210_2135220dup , CM000678.1:g.2135210_2135220dup GRCh37
NC_000016.8:g.2075211_2075221dup NCBI36
NG_005895.1:g.40904_40914dup , LRG_487:g.40904_40914dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2919-21_*2919-11dup ENSP00000455997.2:n.*2919-21_*2919-11dup
ENST00000642206.2:c.4417-21_4417-11dup ENSP00000495146.2:n.4417-21_4417-11dup
ENST00000642365.2:c.4567-21_4567-11dup ENSP00000495459.2:n.4567-21_4567-11dup
ENST00000644417.2:c.*4950-21_*4950-11dup ENSP00000493912.2:n.*4950-21_*4950-11dup
ENST00000646464.2:c.*7319-21_*7319-11dup ENSP00000496610.2:n.*7319-21_*7319-11dup
ENST00000219476.9:c.4570-21_4570-11dup MANE Select ENSP00000219476.3:n.4570-21_4570-11dup
ENST00000350773.9:c.4501-21_4501-11dup ENSP00000344383.4:n.4501-21_4501-11dup
ENST00000401874.7:c.4369-21_4369-11dup ENSP00000384468.2:n.4369-21_4369-11dup
ENST00000568454.6:c.4402-21_4402-11dup ENSP00000454487.1:n.4402-21_4402-11dup
ENST00000569110.2:c.793-21_793-11dup
ENST00000569930.2:n.2452-21_2452-11dup
ENST00000642365.1:c.3224-21_3224-11dup
ENST00000642561.1:c.4441-21_4441-11dup ENSP00000495099.1:n.4441-21_4441-11dup
ENST00000642728.1:n.752-21_752-11dup
ENST00000642791.1:n.146_156dup
ENST00000642797.1:c.4372-21_4372-11dup ENSP00000493846.1:n.4372-21_4372-11dup
ENST00000642936.1:c.4438-21_4438-11dup ENSP00000494514.1:n.4438-21_4438-11dup
ENST00000643088.1:c.4369-27_4369-17dup ENSP00000494747.1:n.4369-27_4369-17dup
ENST00000643177.1:n.584-21_584-11dup
ENST00000643426.1:n.2218-21_2218-11dup
ENST00000643946.1:c.4501-27_4501-17dup ENSP00000495927.1:n.4501-27_4501-17dup
ENST00000644043.1:c.4441-21_4441-11dup ENSP00000496262.1:n.4441-21_4441-11dup
ENST00000644278.1:n.31_41dup
ENST00000644329.1:c.4369-21_4369-11dup ENSP00000496611.1:n.4369-21_4369-11dup
ENST00000644335.1:c.4372-27_4372-17dup ENSP00000496317.1:n.4372-27_4372-17dup
ENST00000644399.1:c.4491-21_4491-11dup
ENST00000645024.1:n.2654-21_2654-11dup
ENST00000646388.1:c.4570-27_4570-17dup ENSP00000495921.1:n.4570-27_4570-17dup
ENST00000646634.1:n.3385-21_3385-11dup
ENST00000646674.1:n.1822-21_1822-11dup
ENST00000647042.1:n.1793-21_1793-11dup
ENST00000647180.1:n.1683-21_1683-11dup
ENST00000219476.7:c.4570-21_4570-11dup ENSP00000219476.3:n.4570-21_4570-11dup
ENST00000350773.8:c.4501-21_4501-11dup ENSP00000344383.4:n.4501-21_4501-11dup
ENST00000382538.10:c.4225-21_4225-11dup ENSP00000371978.6:n.4225-21_4225-11dup
ENST00000401874.6:c.4369-21_4369-11dup ENSP00000384468.2:n.4369-21_4369-11dup
ENST00000439117.6:c.*3737-21_*3737-11dup ENSP00000406980.2:n.*3737-21_*3737-11dup
ENST00000439673.6:c.4261-21_4261-11dup ENSP00000399232.2:n.4261-21_4261-11dup
ENST00000497886.5:n.2328-21_2328-11dup
ENST00000568454.5:c.4402-21_4402-11dup ENSP00000454487.1:n.4402-21_4402-11dup
ENST00000569110.1:c.752-21_752-11dup
ENST00000569930.1:n.1685-21_1685-11dup
NM_000548.3:c.4570-21_4570-11dup , LRG_487t1:c.4570-21_4570-11dup NP_000539.2:n.4570-21_4570-11dup
NM_001077183.1:c.4369-21_4369-11dup NP_001070651.1:n.4369-21_4369-11dup
NM_001114382.1:c.4501-21_4501-11dup NP_001107854.1:n.4501-21_4501-11dup
XM_005255529.3:c.4441-21_4441-11dup XP_005255586.2:n.4441-21_4441-11dup
XM_005255531.3:c.4372-21_4372-11dup XP_005255588.2:n.4372-21_4372-11dup
XM_011522636.1:c.4624-21_4624-11dup XP_011520938.1:n.4624-21_4624-11dup
XM_011522637.1:c.4621-21_4621-11dup XP_011520939.1:n.4621-21_4621-11dup
XM_011522638.1:c.4513-21_4513-11dup XP_011520940.1:n.4513-21_4513-11dup
XM_011522639.1:c.4495-21_4495-11dup XP_011520941.1:n.4495-21_4495-11dup
XM_011522640.1:c.4492-21_4492-11dup XP_011520942.1:n.4492-21_4492-11dup
XM_011522641.1:c.4261-21_4261-11dup XP_011520943.1:n.4261-21_4261-11dup
NM_000548.4:c.4570-21_4570-11dup NP_000539.2:n.4570-21_4570-11dup
NM_001077183.2:c.4369-21_4369-11dup NP_001070651.1:n.4369-21_4369-11dup
NM_001114382.2:c.4501-21_4501-11dup NP_001107854.1:n.4501-21_4501-11dup
NM_001318827.1:c.4261-21_4261-11dup NP_001305756.1:n.4261-21_4261-11dup
NM_001318829.1:c.4225-21_4225-11dup NP_001305758.1:n.4225-21_4225-11dup
NM_001318831.1:c.3838-21_3838-11dup NP_001305760.1:n.3838-21_3838-11dup
NM_001318832.1:c.4402-21_4402-11dup NP_001305761.1:n.4402-21_4402-11dup
NM_001363528.1:c.4372-21_4372-11dup NP_001350457.1:n.4372-21_4372-11dup
NM_021055.2:c.4441-21_4441-11dup NP_066399.2:n.4441-21_4441-11dup
XM_005255531.4:c.4372-21_4372-11dup XP_005255588.2:n.4372-21_4372-11dup
XM_011522636.2:c.4624-21_4624-11dup XP_011520938.1:n.4624-21_4624-11dup
XM_011522637.2:c.4621-21_4621-11dup XP_011520939.1:n.4621-21_4621-11dup
XM_011522638.2:c.4786-21_4786-11dup XP_011520940.2:n.4786-21_4786-11dup
XM_011522639.2:c.4495-21_4495-11dup XP_011520941.1:n.4495-21_4495-11dup
XM_011522640.2:c.4492-21_4492-11dup XP_011520942.1:n.4492-21_4492-11dup
XM_017023615.1:c.4567-21_4567-11dup XP_016879104.1:n.4567-21_4567-11dup
XM_017023616.1:c.4438-21_4438-11dup XP_016879105.1:n.4438-21_4438-11dup
XM_017023617.1:c.4534-21_4534-11dup XP_016879106.1:n.4534-21_4534-11dup
XM_017023618.1:c.3280-21_3280-11dup XP_016879107.1:n.3280-21_3280-11dup
XM_024450413.1:c.4369-21_4369-11dup XP_024306181.1:n.4369-21_4369-11dup
NM_000548.5:c.4570-21_4570-11dup MANE Select NP_000539.2:n.4570-21_4570-11dup
NM_001370404.1:c.4438-21_4438-11dup NP_001357333.1:n.4438-21_4438-11dup
NM_001370405.1:c.4441-21_4441-11dup NP_001357334.1:n.4441-21_4441-11dup
NM_001077183.3:c.4369-21_4369-11dup NP_001070651.1:n.4369-21_4369-11dup
NM_001114382.3:c.4501-21_4501-11dup NP_001107854.1:n.4501-21_4501-11dup
NM_001318827.2:c.4261-21_4261-11dup NP_001305756.1:n.4261-21_4261-11dup
NM_001318829.2:c.4225-21_4225-11dup NP_001305758.1:n.4225-21_4225-11dup
NM_001318831.2:c.3838-21_3838-11dup NP_001305760.1:n.3838-21_3838-11dup
NM_001318832.2:c.4402-21_4402-11dup NP_001305761.1:n.4402-21_4402-11dup
NM_001363528.2:c.4372-21_4372-11dup NP_001350457.1:n.4372-21_4372-11dup
NM_021055.3:c.4441-21_4441-11dup NP_066399.2:n.4441-21_4441-11dup