Canonical Allele Identifier: CA1882406127
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900816G= , CM000671.2:g.132900816G= GRCh38
NC_000009.11:g.135776203G= , CM000671.1:g.135776203G= GRCh37
NC_000009.10:g.134766024G= NCBI36
NG_012386.1:g.48818C= , LRG_486:g.48818C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.2521C= ENSP00000496126.2:p.Gln841=
ENST00000490179.4:c.2524C= ENSP00000495533.2:p.Gln842=
ENST00000642261.2:c.*303C= ENSP00000494743.2:n.*303C=
ENST00000643275.2:c.*464C= ENSP00000495598.2:n.*464C=
ENST00000643362.2:c.2137C= ENSP00000496398.2:p.Gln713=
ENST00000643625.2:c.*266C= ENSP00000495546.2:n.*266C=
ENST00000643691.2:c.2161C= ENSP00000494916.2:p.Gln721=
ENST00000644184.2:c.2482C= ENSP00000495428.2:p.Gln828=
ENST00000645129.2:c.2368C= ENSP00000493639.2:p.Gln790=
ENST00000646440.2:c.2524C= ENSP00000495830.2:p.Gln842=
ENST00000298552.9:c.2524C= MANE Select ENSP00000298552.3:p.Gln842=
ENST00000642261.1:c.584C=
ENST00000642617.1:c.2521C= ENSP00000493773.1:p.Gln841=
ENST00000642627.1:c.2506C= ENSP00000496772.1:p.Gln836=
ENST00000642811.1:c.*2294C= ENSP00000495554.1:n.*2294C=
ENST00000643072.1:c.2371C= ENSP00000496691.1:p.Gln791=
ENST00000643275.1:c.998C= ENSP00000495598.1:n.998C=
ENST00000643583.1:c.2509C= ENSP00000494685.1:p.Gln837=
ENST00000643625.1:c.401C= ENSP00000495546.1:n.401C=
ENST00000643875.1:c.2524C= ENSP00000495158.1:p.Gln842=
ENST00000644097.1:c.2521C= ENSP00000494682.1:p.Gln841=
ENST00000644184.1:c.1219C= ENSP00000495428.1:p.Gln407=
ENST00000644255.1:c.*2291C= ENSP00000493608.1:n.*2291C=
ENST00000644319.1:n.2899C=
ENST00000644786.1:n.183C=
ENST00000644882.1:n.1437C=
ENST00000645901.1:n.3375C=
ENST00000646391.1:c.*2294C= ENSP00000494104.1:n.*2294C=
ENST00000646625.1:c.2524C= ENSP00000496263.1:p.Gln842=
ENST00000647262.1:n.1489C=
ENST00000647279.1:c.*1763C= ENSP00000494502.1:n.*1763C=
ENST00000647506.1:n.3400C=
ENST00000647534.1:n.1588C=
ENST00000298552.7:c.2524C= ENSP00000298552.3:p.Gln842=
ENST00000440111.6:c.2524C= ENSP00000394524.2:p.Gln842=
ENST00000545250.5:c.2371C= ENSP00000444017.1:p.Gln791=
NM_000368.4:c.2524C= , LRG_486t1:c.2524C= NP_000359.1:p.Gln842=
NM_001162426.1:c.2521C= NP_001155898.1:p.Gln841=
NM_001162427.1:c.2371C= NP_001155899.1:p.Gln791=
XM_005272211.1:c.2524C= XP_005272268.1:p.Gln842=
XM_006717271.1:c.2524C= XP_006717334.1:p.Gln842=
XM_011518979.1:c.2524C= XP_011517281.1:p.Gln842=
NM_001362177.1:c.2161C= NP_001349106.1:p.Gln721=
XM_011518979.2:c.2524C= XP_011517281.1:p.Gln842=
XM_017015096.1:c.2524C= XP_016870585.1:p.Gln842=
XM_017015097.1:c.2524C= XP_016870586.1:p.Gln842=
XM_017015098.1:c.2521C= XP_016870587.1:p.Gln841=
XM_017015100.1:c.2161C= XP_016870589.1:p.Gln721=
XM_017015101.1:c.2158C= XP_016870590.1:p.Gln720=
NM_000368.5:c.2524C= MANE Select NP_000359.1:p.Gln842=
NM_001162426.2:c.2521C= NP_001155898.1:p.Gln841=
NM_001162427.2:c.2371C= NP_001155899.1:p.Gln791=
NM_001362177.2:c.2161C= NP_001349106.1:p.Gln721=