Canonical Allele Identifier: CA375369886

Gene: TSC1

Linked Data

• ClinVar Variation Id: 2447898
• ClinVar RCV Id: RCV003176684
• MyVariant Identifiers: chr9:g.135776119G>C (hg19) ; chr9:g.132900732G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900732G>C , CM000671.2:g.132900732G>C	GRCh38
NC_000009.11:g.135776119G>C , CM000671.1:g.135776119G>C	GRCh37
NC_000009.10:g.134765940G>C	NCBI36
NG_012386.1:g.48902C>G , LRG_486:g.48902C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2605C>G	ENSP00000496126.2:p.His869Asp
ENST00000490179.4:c.2608C>G	ENSP00000495533.2:p.His870Asp
ENST00000642261.2:c.*387C>G	ENSP00000494743.2:n.*387C>G
ENST00000643275.2:c.*548C>G	ENSP00000495598.2:n.*548C>G
ENST00000643362.2:c.2221C>G	ENSP00000496398.2:p.His741Asp
ENST00000643625.2:c.*350C>G	ENSP00000495546.2:n.*350C>G
ENST00000643691.2:c.2245C>G	ENSP00000494916.2:p.His749Asp
ENST00000644184.2:c.2566C>G	ENSP00000495428.2:p.His856Asp
ENST00000645129.2:c.2452C>G	ENSP00000493639.2:p.His818Asp
ENST00000646440.2:c.2608C>G	ENSP00000495830.2:p.His870Asp
ENST00000298552.9:c.2608C>G MANE Select	ENSP00000298552.3:p.His870Asp
ENST00000642261.1:c.668C>G
ENST00000642617.1:c.2605C>G	ENSP00000493773.1:p.His869Asp
ENST00000642627.1:c.2590C>G	ENSP00000496772.1:p.His864Asp
ENST00000642811.1:c.*2378C>G	ENSP00000495554.1:n.*2378C>G
ENST00000643072.1:c.2455C>G	ENSP00000496691.1:p.His819Asp
ENST00000643275.1:c.1082C>G	ENSP00000495598.1:n.1082C>G
ENST00000643583.1:c.2593C>G	ENSP00000494685.1:p.His865Asp
ENST00000643625.1:c.485C>G	ENSP00000495546.1:n.485C>G
ENST00000643875.1:c.2608C>G	ENSP00000495158.1:p.His870Asp
ENST00000644097.1:c.2605C>G	ENSP00000494682.1:p.His869Asp
ENST00000644184.1:c.1303C>G	ENSP00000495428.1:p.His435Asp
ENST00000644255.1:c.*2375C>G	ENSP00000493608.1:n.*2375C>G
ENST00000644319.1:n.2983C>G
ENST00000644786.1:n.267C>G
ENST00000644882.1:n.1521C>G
ENST00000645901.1:n.3459C>G
ENST00000646391.1:c.*2378C>G	ENSP00000494104.1:n.*2378C>G
ENST00000646625.1:c.2608C>G	ENSP00000496263.1:p.His870Asp
ENST00000647262.1:n.1573C>G
ENST00000647279.1:c.*1847C>G	ENSP00000494502.1:n.*1847C>G
ENST00000647506.1:n.3484C>G
ENST00000647534.1:n.1672C>G
ENST00000298552.7:c.2608C>G	ENSP00000298552.3:p.His870Asp
ENST00000440111.6:c.2608C>G	ENSP00000394524.2:p.His870Asp
ENST00000545250.5:c.2455C>G	ENSP00000444017.1:p.His819Asp
NM_000368.4:c.2608C>G , LRG_486t1:c.2608C>G	NP_000359.1:p.His870Asp
NM_001162426.1:c.2605C>G	NP_001155898.1:p.His869Asp
NM_001162427.1:c.2455C>G	NP_001155899.1:p.His819Asp
XM_005272211.1:c.2608C>G	XP_005272268.1:p.His870Asp
XM_006717271.1:c.2608C>G	XP_006717334.1:p.His870Asp
XM_011518979.1:c.2608C>G	XP_011517281.1:p.His870Asp
NM_001362177.1:c.2245C>G	NP_001349106.1:p.His749Asp
XM_011518979.2:c.2608C>G	XP_011517281.1:p.His870Asp
XM_017015096.1:c.2608C>G	XP_016870585.1:p.His870Asp
XM_017015097.1:c.2608C>G	XP_016870586.1:p.His870Asp
XM_017015098.1:c.2605C>G	XP_016870587.1:p.His869Asp
XM_017015100.1:c.2245C>G	XP_016870589.1:p.His749Asp
XM_017015101.1:c.2242C>G	XP_016870590.1:p.His748Asp
NM_000368.5:c.2608C>G MANE Select	NP_000359.1:p.His870Asp
NM_001162426.2:c.2605C>G	NP_001155898.1:p.His869Asp
NM_001162427.2:c.2455C>G	NP_001155899.1:p.His819Asp
NM_001362177.2:c.2245C>G	NP_001349106.1:p.His749Asp