Canonical Allele Identifier: CA051851
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283148

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085232_2085237dup , CM000678.2:g.2085232_2085237dup GRCh38
NC_000016.9:g.2135233_2135238dup , CM000678.1:g.2135233_2135238dup GRCh37
NC_000016.8:g.2075234_2075239dup NCBI36
NG_005895.1:g.40927_40932dup , LRG_487:g.40927_40932dup

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*2921_*2926dup
ENST00000642206.2:c.4419_4424dup
ENST00000642365.2:c.4569_4574dup
ENST00000644417.2:c.*4952_*4957dup
ENST00000646464.2:c.*7321_*7326dup
ENST00000219476.9:c.4572_4577dup
ENST00000350773.9:c.4503_4508dup
ENST00000401874.7:c.4371_4376dup
ENST00000568454.6:c.4404_4409dup
ENST00000569110.2:c.795_800dup
ENST00000569930.2:n.2454_2459dup
ENST00000642365.1:c.3226_3231dup
ENST00000642561.1:c.4443_4448dup
ENST00000642728.1:n.754_759dup
ENST00000642791.1:n.169_174dup
ENST00000642797.1:c.4374_4379dup
ENST00000642936.1:c.4440_4445dup
ENST00000643088.1:c.4369-4_4370dup
ENST00000643177.1:n.586_591dup
ENST00000643426.1:n.2220_2225dup
ENST00000643946.1:c.4501-4_4502dup
ENST00000644043.1:c.4443_4448dup
ENST00000644278.1:n.54_59dup
ENST00000644329.1:c.4371_4376dup
ENST00000644335.1:c.4372-4_4373dup
ENST00000644399.1:c.4493_4498dup
ENST00000645024.1:n.2656_2661dup
ENST00000646388.1:c.4570-4_4571dup
ENST00000646634.1:n.3387_3392dup
ENST00000646674.1:n.1824_1829dup
ENST00000647042.1:n.1795_1800dup
ENST00000647180.1:n.1685_1690dup
ENST00000219476.7:c.4572_4577dup
ENST00000350773.8:c.4503_4508dup
ENST00000382538.10:c.4227_4232dup
ENST00000401874.6:c.4371_4376dup
ENST00000439117.6:c.*3739_*3744dup
ENST00000439673.6:c.4263_4268dup
ENST00000497886.5:n.2330_2335dup
ENST00000568454.5:c.4404_4409dup
ENST00000569110.1:c.754_759dup
ENST00000569930.1:n.1687_1692dup
NM_000548.3:c.4572_4577dup , LRG_487t1:c.4572_4577dup
NM_001077183.1:c.4371_4376dup
NM_001114382.1:c.4503_4508dup
XM_005255529.3:c.4443_4448dup
XM_005255531.3:c.4374_4379dup
XM_011522636.1:c.4626_4631dup
XM_011522637.1:c.4623_4628dup
XM_011522638.1:c.4515_4520dup
XM_011522639.1:c.4497_4502dup
XM_011522640.1:c.4494_4499dup
XM_011522641.1:c.4263_4268dup
NM_000548.4:c.4572_4577dup
NM_001077183.2:c.4371_4376dup
NM_001114382.2:c.4503_4508dup
NM_001318827.1:c.4263_4268dup
NM_001318829.1:c.4227_4232dup
NM_001318831.1:c.3840_3845dup
NM_001318832.1:c.4404_4409dup
NM_001363528.1:c.4374_4379dup
NM_021055.2:c.4443_4448dup
XM_005255531.4:c.4374_4379dup
XM_011522636.2:c.4626_4631dup
XM_011522637.2:c.4623_4628dup
XM_011522638.2:c.4788_4793dup
XM_011522639.2:c.4497_4502dup
XM_011522640.2:c.4494_4499dup
XM_017023615.1:c.4569_4574dup
XM_017023616.1:c.4440_4445dup
XM_017023617.1:c.4536_4541dup
XM_017023618.1:c.3282_3287dup
XM_024450413.1:c.4371_4376dup
NM_000548.5:c.4572_4577dup
NM_001370404.1:c.4440_4445dup
NM_001370405.1:c.4443_4448dup
NM_001077183.3:c.4371_4376dup
NM_001114382.3:c.4503_4508dup
NM_001318827.2:c.4263_4268dup
NM_001318829.2:c.4227_4232dup
NM_001318831.2:c.3840_3845dup
NM_001318832.2:c.4404_4409dup
NM_001363528.2:c.4374_4379dup
NM_021055.3:c.4443_4448dup