Canonical Allele Identifier: CA16043438
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374172
ClinVar RCV Id: RCV000415178
dbSNP Id: rs1057518945
MyVariant Identifiers: chr9:g.135797211del (hg19) chr9:g.132921824del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132921825del , CM000671.2:g.132921825del GRCh38
NC_000009.11:g.135797212del , CM000671.1:g.135797212del GRCh37
NC_000009.10:g.134787033del NCBI36
NG_012386.1:g.27810del , LRG_486:g.27810del

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.658del ENSP00000496126.2:p.Val220SerfsTer4
ENST00000490179.4:c.658del ENSP00000495533.2:p.Val220SerfsTer4
ENST00000642261.2:c.658del ENSP00000494743.2:p.Val220SerfsTer4
ENST00000643275.2:c.658del ENSP00000495598.2:p.Val220SerfsTer4
ENST00000643362.2:c.505del ENSP00000496398.2:p.Val169SerfsTer4
ENST00000643625.2:c.658del ENSP00000495546.2:p.Val220SerfsTer4
ENST00000643691.2:c.295del ENSP00000494916.2:p.Val99SerfsTer4
ENST00000644184.2:c.658del ENSP00000495428.2:p.Val220SerfsTer4
ENST00000645129.2:c.505del ENSP00000493639.2:p.Val169SerfsTer4
ENST00000646440.2:c.658del ENSP00000495830.2:p.Val220SerfsTer4
ENST00000647078.2:c.658del ENSP00000496066.1:p.Val220SerfsTer4
ENST00000298552.9:c.658del MANE Select ENSP00000298552.3:p.Val220SerfsTer4
ENST00000403810.6:c.658del ENSP00000386093.1:p.Val220SerfsTer4
ENST00000475903.6:c.658del ENSP00000496126.1:p.Val220SerfsTer4
ENST00000642344.1:c.*399del ENSP00000494847.1:n.*399del
ENST00000642617.1:c.658del ENSP00000493773.1:p.Val220SerfsTer4
ENST00000642627.1:c.658del ENSP00000496772.1:p.Val220SerfsTer4
ENST00000642646.1:c.658del ENSP00000496292.1:p.Val220SerfsTer4
ENST00000642745.1:c.658del ENSP00000493963.1:p.Val220SerfsTer4
ENST00000642811.1:c.*428del ENSP00000495554.1:n.*428del
ENST00000642854.1:c.*443del ENSP00000494639.1:n.*443del
ENST00000643072.1:c.505del ENSP00000496691.1:p.Val169SerfsTer4
ENST00000643362.1:c.505del ENSP00000496398.1:p.Val169SerfsTer4
ENST00000643583.1:c.658del ENSP00000494685.1:p.Val220SerfsTer4
ENST00000643691.1:c.295del ENSP00000494916.1:p.Val99SerfsTer4
ENST00000643875.1:c.658del ENSP00000495158.1:p.Val220SerfsTer4
ENST00000644097.1:c.658del ENSP00000494682.1:p.Val220SerfsTer4
ENST00000644255.1:c.*428del ENSP00000493608.1:n.*428del
ENST00000644997.1:c.*315del ENSP00000495654.1:n.*315del
ENST00000645129.1:c.505del ENSP00000493639.1:p.Val169SerfsTer4
ENST00000645150.1:c.658del ENSP00000494365.1:p.Val220SerfsTer4
ENST00000645901.1:n.861del
ENST00000646391.1:c.*428del ENSP00000494104.1:n.*428del
ENST00000646625.1:c.658del ENSP00000496263.1:p.Val220SerfsTer4
ENST00000647078.1:c.658del ENSP00000496066.1:p.Val220SerfsTer4
ENST00000647279.1:c.658del ENSP00000494502.1:p.Val220SerfsTer?
ENST00000647462.1:c.658del ENSP00000495821.1:p.Val220SerfsTer4
ENST00000647506.1:n.886del
ENST00000298552.7:c.658del ENSP00000298552.3:p.Val220SerfsTer4
ENST00000403810.5:c.658del ENSP00000386093.1:p.Val220SerfsTer4
ENST00000440111.6:c.658del ENSP00000394524.2:p.Val220SerfsTer4
ENST00000461879.5:n.487del
ENST00000475903.5:n.815del
ENST00000493467.5:n.854del
ENST00000545250.5:c.505del ENSP00000444017.1:p.Val169SerfsTer4
NM_000368.4:c.658del , LRG_486t1:c.658del NP_000359.1:p.Val220SerfsTer4
NM_001162426.1:c.658del NP_001155898.1:p.Val220SerfsTer4
NM_001162427.1:c.505del NP_001155899.1:p.Val169SerfsTer4
XM_005272211.1:c.658del XP_005272268.1:p.Val220SerfsTer4
XM_006717271.1:c.658del XP_006717334.1:p.Val220SerfsTer4
XM_006717272.2:c.658del XP_006717335.1:p.Val220SerfsTer4
XM_011518979.1:c.658del XP_011517281.1:p.Val220SerfsTer4
NM_001362177.1:c.295del NP_001349106.1:p.Val99SerfsTer4
XM_011518979.2:c.658del XP_011517281.1:p.Val220SerfsTer4
XM_017015096.1:c.658del XP_016870585.1:p.Val220SerfsTer4
XM_017015097.1:c.658del XP_016870586.1:p.Val220SerfsTer4
XM_017015098.1:c.658del XP_016870587.1:p.Val220SerfsTer4
XM_017015100.1:c.295del XP_016870589.1:p.Val99SerfsTer4
XM_017015101.1:c.295del XP_016870590.1:p.Val99SerfsTer4
NM_000368.5:c.658del MANE Select NP_000359.1:p.Val220SerfsTer4
NM_001162426.2:c.658del NP_001155898.1:p.Val220SerfsTer4
NM_001162427.2:c.505del NP_001155899.1:p.Val169SerfsTer4
NM_001362177.2:c.295del NP_001349106.1:p.Val99SerfsTer4
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