Canonical Allele Identifier: CA1139664254
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 960057
ClinVar RCV Id: RCV001233512
dbSNP Id: rs137854397

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088318_2088344dup , CM000678.2:g.2088318_2088344dup GRCh38
NC_000016.9:g.2138319_2138345dup , CM000678.1:g.2138319_2138345dup GRCh37
NC_000016.8:g.2078320_2078346dup NCBI36
NG_005895.1:g.44013_44039dup , LRG_487:g.44013_44039dup
NG_008617.1:g.54883_54909dup

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*3601_*3608+19dup
ENST00000642206.2:c.5099_5106+19dup
ENST00000642365.2:c.5249_5256+19dup
ENST00000644417.2:c.*5765_*5772+19dup
ENST00000646464.2:c.*8001_*8008+19dup
ENST00000219476.9:c.5252_5259+19dup
ENST00000350773.9:c.5183_5190+19dup
ENST00000401874.7:c.5051_5058+19dup
ENST00000568454.6:c.5084_5091+19dup
ENST00000569110.2:c.1475_1482+19dup
ENST00000569930.2:n.3134_3141+19dup
ENST00000642365.1:c.3906_3913+19dup
ENST00000642561.1:c.5111_5118+19dup
ENST00000642791.1:n.849_856+19dup
ENST00000642797.1:c.5054_5061+19dup
ENST00000642936.1:c.5120_5127+19dup
ENST00000643088.1:c.5045_5052+19dup
ENST00000643426.1:n.2900_2907+19dup
ENST00000643946.1:c.5177_5184+19dup
ENST00000644043.1:c.5123_5130+19dup
ENST00000644329.1:c.5138_5145+19dup
ENST00000644335.1:c.5048_5055+19dup
ENST00000644399.1:c.5173_5180+19dup
ENST00000645024.1:n.3336_3343+19dup
ENST00000646388.1:c.5246_5253+19dup
ENST00000646634.1:n.4067_4074+19dup
ENST00000646674.1:n.2504_2511+19dup
ENST00000647042.1:n.2475_2482+19dup
ENST00000647180.1:n.2365_2372+19dup
ENST00000219476.7:c.5252_5259+19dup
ENST00000350773.8:c.5183_5190+19dup
ENST00000382538.10:c.4907_4914+19dup
ENST00000401874.6:c.5051_5058+19dup
ENST00000439117.6:c.*4419_*4426+19dup
ENST00000439673.6:c.4943_4950+19dup
ENST00000497886.5:n.2975_2982+19dup
ENST00000568454.5:c.5084_5091+19dup
ENST00000569110.1:c.1434_1441+19dup
ENST00000569930.1:n.2367_2374+19dup
NM_000548.3:c.5252_5259+19dup , LRG_487t1:c.5252_5259+19dup
NM_001077183.1:c.5051_5058+19dup
NM_001114382.1:c.5183_5190+19dup
XM_005255529.3:c.5123_5130+19dup
XM_005255531.3:c.5054_5061+19dup
XM_011522636.1:c.5306_5313+19dup
XM_011522637.1:c.5303_5310+19dup
XM_011522638.1:c.5195_5202+19dup
XM_011522639.1:c.5177_5184+19dup
XM_011522640.1:c.5174_5181+19dup
XM_011522641.1:c.4943_4950+19dup
NM_000548.4:c.5252_5259+19dup
NM_001077183.2:c.5051_5058+19dup
NM_001114382.2:c.5183_5190+19dup
NM_001318827.1:c.4943_4950+19dup
NM_001318829.1:c.4907_4914+19dup
NM_001318831.1:c.4520_4527+19dup
NM_001318832.1:c.5084_5091+19dup
NM_001363528.1:c.5054_5061+19dup
NM_021055.2:c.5123_5130+19dup
XM_005255531.4:c.5054_5061+19dup
XM_011522636.2:c.5306_5313+19dup
XM_011522637.2:c.5303_5310+19dup
XM_011522638.2:c.5468_5475+19dup
XM_011522639.2:c.5177_5184+19dup
XM_011522640.2:c.5174_5181+19dup
XM_017023615.1:c.5249_5256+19dup
XM_017023616.1:c.5120_5127+19dup
XM_017023617.1:c.5216_5223+19dup
XM_017023618.1:c.3962_3969+19dup
XM_024450413.1:c.5138_5145+19dup
NM_000548.5:c.5252_5259+19dup
NM_001370404.1:c.5120_5127+19dup
NM_001370405.1:c.5111_5118+19dup
NM_001077183.3:c.5051_5058+19dup
NM_001114382.3:c.5183_5190+19dup
NM_001318827.2:c.4943_4950+19dup
NM_001318829.2:c.4907_4914+19dup
NM_001318831.2:c.4520_4527+19dup
NM_001318832.2:c.5084_5091+19dup
NM_001363528.2:c.5054_5061+19dup
NM_021055.3:c.5123_5130+19dup