Canonical Allele Identifier: CA1882409604
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132902776C= , CM000671.2:g.132902776C= GRCh38
NC_000009.11:g.135778163C= , CM000671.1:g.135778163C= GRCh37
NC_000009.10:g.134767984C= NCBI36
NG_012386.1:g.46858G= , LRG_486:g.46858G=

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.2217G= ENSP00000496126.2:p.Leu739=
ENST00000490179.4:c.2220G= ENSP00000495533.2:p.Leu740=
ENST00000642261.2:c.2216G= ENSP00000494743.2:p.Ter739=
ENST00000643275.2:c.*160G= ENSP00000495598.2:n.*160G=
ENST00000643362.2:c.1833G= ENSP00000496398.2:p.Leu611=
ENST00000643625.2:c.2053G= ENSP00000495546.2:p.Glu685=
ENST00000643691.2:c.1857G= ENSP00000494916.2:p.Leu619=
ENST00000644184.2:c.2220G= ENSP00000495428.2:p.Leu740=
ENST00000645129.2:c.2064G= ENSP00000493639.2:p.Leu688=
ENST00000646440.2:c.2220G= ENSP00000495830.2:p.Leu740=
ENST00000298552.9:c.2220G= MANE Select ENSP00000298552.3:p.Leu740=
ENST00000642261.1:c.280G=
ENST00000642617.1:c.2217G= ENSP00000493773.1:p.Leu739=
ENST00000642627.1:c.2202G= ENSP00000496772.1:p.Leu734=
ENST00000642811.1:c.*1990G= ENSP00000495554.1:n.*1990G=
ENST00000643072.1:c.2067G= ENSP00000496691.1:p.Leu689=
ENST00000643275.1:c.694G= ENSP00000495598.1:n.694G=
ENST00000643583.1:c.2205G= ENSP00000494685.1:p.Leu735=
ENST00000643625.1:c.97G= ENSP00000495546.1:p.Glu33=
ENST00000643875.1:c.2220G= ENSP00000495158.1:p.Leu740=
ENST00000644097.1:c.2217G= ENSP00000494682.1:p.Leu739=
ENST00000644184.1:c.957G= ENSP00000495428.1:p.Leu319=
ENST00000644255.1:c.*1987G= ENSP00000493608.1:n.*1987G=
ENST00000644319.1:n.2595G=
ENST00000644882.1:n.1175G=
ENST00000645901.1:n.3071G=
ENST00000646391.1:c.*1990G= ENSP00000494104.1:n.*1990G=
ENST00000646625.1:c.2220G= ENSP00000496263.1:p.Leu740=
ENST00000647262.1:n.1185G=
ENST00000647279.1:c.*1459G= ENSP00000494502.1:n.*1459G=
ENST00000647506.1:n.3096G=
ENST00000647534.1:n.1284G=
ENST00000298552.7:c.2220G= ENSP00000298552.3:p.Leu740=
ENST00000440111.6:c.2220G= ENSP00000394524.2:p.Leu740=
ENST00000545250.5:c.2067G= ENSP00000444017.1:p.Leu689=
NM_000368.4:c.2220G= , LRG_486t1:c.2220G= NP_000359.1:p.Leu740=
NM_001162426.1:c.2217G= NP_001155898.1:p.Leu739=
NM_001162427.1:c.2067G= NP_001155899.1:p.Leu689=
XM_005272211.1:c.2220G= XP_005272268.1:p.Leu740=
XM_006717271.1:c.2220G= XP_006717334.1:p.Leu740=
XM_011518979.1:c.2220G= XP_011517281.1:p.Leu740=
NM_001362177.1:c.1857G= NP_001349106.1:p.Leu619=
XM_011518979.2:c.2220G= XP_011517281.1:p.Leu740=
XM_017015096.1:c.2220G= XP_016870585.1:p.Leu740=
XM_017015097.1:c.2220G= XP_016870586.1:p.Leu740=
XM_017015098.1:c.2217G= XP_016870587.1:p.Leu739=
XM_017015100.1:c.1857G= XP_016870589.1:p.Leu619=
XM_017015101.1:c.1854G= XP_016870590.1:p.Leu618=
NM_000368.5:c.2220G= MANE Select NP_000359.1:p.Leu740=
NM_001162426.2:c.2217G= NP_001155898.1:p.Leu739=
NM_001162427.2:c.2067G= NP_001155899.1:p.Leu689=
NM_001362177.2:c.1857G= NP_001349106.1:p.Leu619=