Canonical Allele Identifier: CA1882417496
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132911461_132911462delinsGT , CM000671.2:g.132911461_132911462delinsGT GRCh38
NC_000009.11:g.135786848_135786849delinsGT , CM000671.1:g.135786848_135786849delinsGT GRCh37
NC_000009.10:g.134776669_134776670delinsGT NCBI36
NG_012386.1:g.38172_38173delinsAC , LRG_486:g.38172_38173delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.1020_1021delinsAC ENSP00000496126.2:p.Glu340=
ENST00000490179.4:c.1020_1021delinsAC ENSP00000495533.2:p.Glu340=
ENST00000642261.2:c.1020_1021delinsAC ENSP00000494743.2:p.Glu340=
ENST00000643275.2:c.1020_1021delinsAC ENSP00000495598.2:p.Glu340=
ENST00000643362.2:c.867_868delinsAC ENSP00000496398.2:p.Glu289=
ENST00000643625.2:c.1020_1021delinsAC ENSP00000495546.2:p.Glu340=
ENST00000643691.2:c.657_658delinsAC ENSP00000494916.2:p.Glu219=
ENST00000644184.2:c.1020_1021delinsAC ENSP00000495428.2:p.Glu340=
ENST00000645129.2:c.867_868delinsAC ENSP00000493639.2:p.Glu289=
ENST00000646440.2:c.1020_1021delinsAC ENSP00000495830.2:p.Glu340=
ENST00000647078.2:c.1020_1021delinsAC ENSP00000496066.1:p.Glu340=
ENST00000298552.9:c.1020_1021delinsAC MANE Select ENSP00000298552.3:p.Glu340=
ENST00000403810.6:c.1020_1021delinsAC ENSP00000386093.1:p.Glu340=
ENST00000493467.6:n.294_295delinsAC
ENST00000642344.1:c.*761_*762delinsAC ENSP00000494847.1:n.*761_*762delinsAC
ENST00000642617.1:c.1020_1021delinsAC ENSP00000493773.1:p.Glu340=
ENST00000642627.1:c.1020_1021delinsAC ENSP00000496772.1:p.Glu340=
ENST00000642646.1:c.1020_1021delinsAC ENSP00000496292.1:p.Glu340=
ENST00000642745.1:c.1020_1021delinsAC ENSP00000493963.1:p.Glu340=
ENST00000642811.1:c.*790_*791delinsAC ENSP00000495554.1:n.*790_*791delinsAC
ENST00000642854.1:c.*805_*806delinsAC ENSP00000494639.1:n.*805_*806delinsAC
ENST00000643072.1:c.867_868delinsAC ENSP00000496691.1:p.Glu289=
ENST00000643362.1:c.867_868delinsAC ENSP00000496398.1:p.Glu289=
ENST00000643583.1:c.1020_1021delinsAC ENSP00000494685.1:p.Glu340=
ENST00000643875.1:c.1020_1021delinsAC ENSP00000495158.1:p.Glu340=
ENST00000644097.1:c.1020_1021delinsAC ENSP00000494682.1:p.Glu340=
ENST00000644255.1:c.*790_*791delinsAC ENSP00000493608.1:n.*790_*791delinsAC
ENST00000644319.1:n.747_748delinsAC
ENST00000644997.1:c.*677_*678delinsAC ENSP00000495654.1:n.*677_*678delinsAC
ENST00000645129.1:c.867_868delinsAC ENSP00000493639.1:p.Glu289=
ENST00000645150.1:c.1020_1021delinsAC ENSP00000494365.1:p.Glu340=
ENST00000645901.1:n.1223_1224delinsAC
ENST00000646391.1:c.*790_*791delinsAC ENSP00000494104.1:n.*790_*791delinsAC
ENST00000646625.1:c.1020_1021delinsAC ENSP00000496263.1:p.Glu340=
ENST00000647078.1:c.1020_1021delinsAC ENSP00000496066.1:p.Glu340=
ENST00000647279.1:c.*259_*260delinsAC ENSP00000494502.1:n.*259_*260delinsAC
ENST00000647462.1:c.1020_1021delinsAC ENSP00000495821.1:p.Glu340=
ENST00000647506.1:n.1248_1249delinsAC
ENST00000298552.7:c.1020_1021delinsAC ENSP00000298552.3:p.Glu340=
ENST00000403810.5:c.1020_1021delinsAC ENSP00000386093.1:p.Glu340=
ENST00000440111.6:c.1020_1021delinsAC ENSP00000394524.2:p.Glu340=
ENST00000493467.5:n.1216_1217delinsAC
ENST00000545250.5:c.867_868delinsAC ENSP00000444017.1:p.Glu289=
NM_000368.4:c.1020_1021delinsAC , LRG_486t1:c.1020_1021delinsAC NP_000359.1:p.Glu340=
NM_001162426.1:c.1020_1021delinsAC NP_001155898.1:p.Glu340=
NM_001162427.1:c.867_868delinsAC NP_001155899.1:p.Glu289=
XM_005272211.1:c.1020_1021delinsAC XP_005272268.1:p.Glu340=
XM_006717271.1:c.1020_1021delinsAC XP_006717334.1:p.Glu340=
XM_006717272.2:c.1020_1021delinsAC XP_006717335.1:p.Glu340=
XM_011518979.1:c.1020_1021delinsAC XP_011517281.1:p.Glu340=
NM_001362177.1:c.657_658delinsAC NP_001349106.1:p.Glu219=
XM_011518979.2:c.1020_1021delinsAC XP_011517281.1:p.Glu340=
XM_017015096.1:c.1020_1021delinsAC XP_016870585.1:p.Glu340=
XM_017015097.1:c.1020_1021delinsAC XP_016870586.1:p.Glu340=
XM_017015098.1:c.1020_1021delinsAC XP_016870587.1:p.Glu340=
XM_017015100.1:c.657_658delinsAC XP_016870589.1:p.Glu219=
XM_017015101.1:c.657_658delinsAC XP_016870590.1:p.Glu219=
NM_000368.5:c.1020_1021delinsAC MANE Select NP_000359.1:p.Glu340=
NM_001162426.2:c.1020_1021delinsAC NP_001155898.1:p.Glu340=
NM_001162427.2:c.867_868delinsAC NP_001155899.1:p.Glu289=
NM_001362177.2:c.657_658delinsAC NP_001349106.1:p.Glu219=