Canonical Allele Identifier: CA1882405898
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900747G= , CM000671.2:g.132900747G= GRCh38
NC_000009.11:g.135776134G= , CM000671.1:g.135776134G= GRCh37
NC_000009.10:g.134765955G= NCBI36
NG_012386.1:g.48887C= , LRG_486:g.48887C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.2590C= ENSP00000496126.2:p.Gln864=
ENST00000490179.4:c.2593C= ENSP00000495533.2:p.Gln865=
ENST00000642261.2:c.*372C= ENSP00000494743.2:n.*372C=
ENST00000643275.2:c.*533C= ENSP00000495598.2:n.*533C=
ENST00000643362.2:c.2206C= ENSP00000496398.2:p.Gln736=
ENST00000643625.2:c.*335C= ENSP00000495546.2:n.*335C=
ENST00000643691.2:c.2230C= ENSP00000494916.2:p.Gln744=
ENST00000644184.2:c.2551C= ENSP00000495428.2:p.Gln851=
ENST00000645129.2:c.2437C= ENSP00000493639.2:p.Gln813=
ENST00000646440.2:c.2593C= ENSP00000495830.2:p.Gln865=
ENST00000298552.9:c.2593C= MANE Select ENSP00000298552.3:p.Gln865=
ENST00000642261.1:c.653C=
ENST00000642617.1:c.2590C= ENSP00000493773.1:p.Gln864=
ENST00000642627.1:c.2575C= ENSP00000496772.1:p.Gln859=
ENST00000642811.1:c.*2363C= ENSP00000495554.1:n.*2363C=
ENST00000643072.1:c.2440C= ENSP00000496691.1:p.Gln814=
ENST00000643275.1:c.1067C= ENSP00000495598.1:n.1067C=
ENST00000643583.1:c.2578C= ENSP00000494685.1:p.Gln860=
ENST00000643625.1:c.470C= ENSP00000495546.1:n.470C=
ENST00000643875.1:c.2593C= ENSP00000495158.1:p.Gln865=
ENST00000644097.1:c.2590C= ENSP00000494682.1:p.Gln864=
ENST00000644184.1:c.1288C= ENSP00000495428.1:p.Gln430=
ENST00000644255.1:c.*2360C= ENSP00000493608.1:n.*2360C=
ENST00000644319.1:n.2968C=
ENST00000644786.1:n.252C=
ENST00000644882.1:n.1506C=
ENST00000645901.1:n.3444C=
ENST00000646391.1:c.*2363C= ENSP00000494104.1:n.*2363C=
ENST00000646625.1:c.2593C= ENSP00000496263.1:p.Gln865=
ENST00000647262.1:n.1558C=
ENST00000647279.1:c.*1832C= ENSP00000494502.1:n.*1832C=
ENST00000647506.1:n.3469C=
ENST00000647534.1:n.1657C=
ENST00000298552.7:c.2593C= ENSP00000298552.3:p.Gln865=
ENST00000440111.6:c.2593C= ENSP00000394524.2:p.Gln865=
ENST00000545250.5:c.2440C= ENSP00000444017.1:p.Gln814=
NM_000368.4:c.2593C= , LRG_486t1:c.2593C= NP_000359.1:p.Gln865=
NM_001162426.1:c.2590C= NP_001155898.1:p.Gln864=
NM_001162427.1:c.2440C= NP_001155899.1:p.Gln814=
XM_005272211.1:c.2593C= XP_005272268.1:p.Gln865=
XM_006717271.1:c.2593C= XP_006717334.1:p.Gln865=
XM_011518979.1:c.2593C= XP_011517281.1:p.Gln865=
NM_001362177.1:c.2230C= NP_001349106.1:p.Gln744=
XM_011518979.2:c.2593C= XP_011517281.1:p.Gln865=
XM_017015096.1:c.2593C= XP_016870585.1:p.Gln865=
XM_017015097.1:c.2593C= XP_016870586.1:p.Gln865=
XM_017015098.1:c.2590C= XP_016870587.1:p.Gln864=
XM_017015100.1:c.2230C= XP_016870589.1:p.Gln744=
XM_017015101.1:c.2227C= XP_016870590.1:p.Gln743=
NM_000368.5:c.2593C= MANE Select NP_000359.1:p.Gln865=
NM_001162426.2:c.2590C= NP_001155898.1:p.Gln864=
NM_001162427.2:c.2440C= NP_001155899.1:p.Gln814=
NM_001362177.2:c.2230C= NP_001349106.1:p.Gln744=