Canonical Allele Identifier: CA1882410776
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132903687G= , CM000671.2:g.132903687G= GRCh38
NC_000009.11:g.135779074G= , CM000671.1:g.135779074G= GRCh37
NC_000009.10:g.134768895G= NCBI36
NG_012386.1:g.45947C= , LRG_486:g.45947C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2169C= ENSP00000496126.2:p.Ile723=
ENST00000490179.4:c.2172C= ENSP00000495533.2:p.Ile724=
ENST00000642261.2:c.2172C= ENSP00000494743.2:p.Ile724=
ENST00000643275.2:c.*112C= ENSP00000495598.2:n.*112C=
ENST00000643362.2:c.1785C= ENSP00000496398.2:p.Ile595=
ENST00000643625.2:c.2041+724C= ENSP00000495546.2:n.2041+724C=
ENST00000643691.2:c.1809C= ENSP00000494916.2:p.Ile603=
ENST00000644184.2:c.2172C= ENSP00000495428.2:p.Ile724=
ENST00000645129.2:c.2016C= ENSP00000493639.2:p.Ile672=
ENST00000646440.2:c.2172C= ENSP00000495830.2:p.Ile724=
ENST00000298552.9:c.2172C= MANE Select ENSP00000298552.3:p.Ile724=
ENST00000642261.1:c.236C=
ENST00000642617.1:c.2169C= ENSP00000493773.1:p.Ile723=
ENST00000642627.1:c.2154C= ENSP00000496772.1:p.Ile718=
ENST00000642811.1:c.*1942C= ENSP00000495554.1:n.*1942C=
ENST00000643072.1:c.2019C= ENSP00000496691.1:p.Ile673=
ENST00000643275.1:c.646C= ENSP00000495598.1:n.646C=
ENST00000643583.1:c.2157C= ENSP00000494685.1:p.Ile719=
ENST00000643625.1:c.85+724C= ENSP00000495546.1:n.85+724C=
ENST00000643875.1:c.2172C= ENSP00000495158.1:p.Ile724=
ENST00000644097.1:c.2169C= ENSP00000494682.1:p.Ile723=
ENST00000644184.1:c.909C= ENSP00000495428.1:p.Ile303=
ENST00000644255.1:c.*1939C= ENSP00000493608.1:n.*1939C=
ENST00000644319.1:n.2547C=
ENST00000644882.1:n.1127C=
ENST00000645901.1:n.3023C=
ENST00000646391.1:c.*1942C= ENSP00000494104.1:n.*1942C=
ENST00000646625.1:c.2172C= ENSP00000496263.1:p.Ile724=
ENST00000647262.1:n.1137C=
ENST00000647279.1:c.*1411C= ENSP00000494502.1:n.*1411C=
ENST00000647506.1:n.3048C=
ENST00000647534.1:n.1236C=
ENST00000298552.7:c.2172C= ENSP00000298552.3:p.Ile724=
ENST00000440111.6:c.2172C= ENSP00000394524.2:p.Ile724=
ENST00000545250.5:c.2019C= ENSP00000444017.1:p.Ile673=
NM_000368.4:c.2172C= , LRG_486t1:c.2172C= NP_000359.1:p.Ile724=
NM_001162426.1:c.2169C= NP_001155898.1:p.Ile723=
NM_001162427.1:c.2019C= NP_001155899.1:p.Ile673=
XM_005272211.1:c.2172C= XP_005272268.1:p.Ile724=
XM_006717271.1:c.2172C= XP_006717334.1:p.Ile724=
XM_011518979.1:c.2172C= XP_011517281.1:p.Ile724=
NM_001362177.1:c.1809C= NP_001349106.1:p.Ile603=
XM_011518979.2:c.2172C= XP_011517281.1:p.Ile724=
XM_017015096.1:c.2172C= XP_016870585.1:p.Ile724=
XM_017015097.1:c.2172C= XP_016870586.1:p.Ile724=
XM_017015098.1:c.2169C= XP_016870587.1:p.Ile723=
XM_017015100.1:c.1809C= XP_016870589.1:p.Ile603=
XM_017015101.1:c.1806C= XP_016870590.1:p.Ile602=
NM_000368.5:c.2172C= MANE Select NP_000359.1:p.Ile724=
NM_001162426.2:c.2169C= NP_001155898.1:p.Ile723=
NM_001162427.2:c.2019C= NP_001155899.1:p.Ile673=
NM_001362177.2:c.1809C= NP_001349106.1:p.Ile603=