Canonical Allele Identifier: CA1882410702
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132903676G= , CM000671.2:g.132903676G= GRCh38
NC_000009.11:g.135779063G= , CM000671.1:g.135779063G= GRCh37
NC_000009.10:g.134768884G= NCBI36
NG_012386.1:g.45958C= , LRG_486:g.45958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2180C= ENSP00000496126.2:p.Ala727=
ENST00000490179.4:c.2183C= ENSP00000495533.2:p.Ala728=
ENST00000642261.2:c.2183C= ENSP00000494743.2:p.Ala728=
ENST00000643275.2:c.*123C= ENSP00000495598.2:n.*123C=
ENST00000643362.2:c.1796C= ENSP00000496398.2:p.Ala599=
ENST00000643625.2:c.2041+735C= ENSP00000495546.2:n.2041+735C=
ENST00000643691.2:c.1820C= ENSP00000494916.2:p.Ala607=
ENST00000644184.2:c.2183C= ENSP00000495428.2:p.Ala728=
ENST00000645129.2:c.2027C= ENSP00000493639.2:p.Ala676=
ENST00000646440.2:c.2183C= ENSP00000495830.2:p.Ala728=
ENST00000298552.9:c.2183C= MANE Select ENSP00000298552.3:p.Ala728=
ENST00000642261.1:c.247C=
ENST00000642617.1:c.2180C= ENSP00000493773.1:p.Ala727=
ENST00000642627.1:c.2165C= ENSP00000496772.1:p.Ala722=
ENST00000642811.1:c.*1953C= ENSP00000495554.1:n.*1953C=
ENST00000643072.1:c.2030C= ENSP00000496691.1:p.Ala677=
ENST00000643275.1:c.657C= ENSP00000495598.1:n.657C=
ENST00000643583.1:c.2168C= ENSP00000494685.1:p.Ala723=
ENST00000643625.1:c.85+735C= ENSP00000495546.1:n.85+735C=
ENST00000643875.1:c.2183C= ENSP00000495158.1:p.Ala728=
ENST00000644097.1:c.2180C= ENSP00000494682.1:p.Ala727=
ENST00000644184.1:c.920C= ENSP00000495428.1:p.Ala307=
ENST00000644255.1:c.*1950C= ENSP00000493608.1:n.*1950C=
ENST00000644319.1:n.2558C=
ENST00000644882.1:n.1138C=
ENST00000645901.1:n.3034C=
ENST00000646391.1:c.*1953C= ENSP00000494104.1:n.*1953C=
ENST00000646625.1:c.2183C= ENSP00000496263.1:p.Ala728=
ENST00000647262.1:n.1148C=
ENST00000647279.1:c.*1422C= ENSP00000494502.1:n.*1422C=
ENST00000647506.1:n.3059C=
ENST00000647534.1:n.1247C=
ENST00000298552.7:c.2183C= ENSP00000298552.3:p.Ala728=
ENST00000440111.6:c.2183C= ENSP00000394524.2:p.Ala728=
ENST00000545250.5:c.2030C= ENSP00000444017.1:p.Ala677=
NM_000368.4:c.2183C= , LRG_486t1:c.2183C= NP_000359.1:p.Ala728=
NM_001162426.1:c.2180C= NP_001155898.1:p.Ala727=
NM_001162427.1:c.2030C= NP_001155899.1:p.Ala677=
XM_005272211.1:c.2183C= XP_005272268.1:p.Ala728=
XM_006717271.1:c.2183C= XP_006717334.1:p.Ala728=
XM_011518979.1:c.2183C= XP_011517281.1:p.Ala728=
NM_001362177.1:c.1820C= NP_001349106.1:p.Ala607=
XM_011518979.2:c.2183C= XP_011517281.1:p.Ala728=
XM_017015096.1:c.2183C= XP_016870585.1:p.Ala728=
XM_017015097.1:c.2183C= XP_016870586.1:p.Ala728=
XM_017015098.1:c.2180C= XP_016870587.1:p.Ala727=
XM_017015100.1:c.1820C= XP_016870589.1:p.Ala607=
XM_017015101.1:c.1817C= XP_016870590.1:p.Ala606=
NM_000368.5:c.2183C= MANE Select NP_000359.1:p.Ala728=
NM_001162426.2:c.2180C= NP_001155898.1:p.Ala727=
NM_001162427.2:c.2030C= NP_001155899.1:p.Ala677=
NM_001362177.2:c.1820C= NP_001349106.1:p.Ala607=