Canonical Allele Identifier: CA375360942

Gene: TSC1

Linked Data

• dbSNP Id: rs1554815286
• MyVariant Identifiers: chr9:g.135779110A>C (hg19) ; chr9:g.132903723A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903723A>C , CM000671.2:g.132903723A>C	GRCh38
NC_000009.11:g.135779110A>C , CM000671.1:g.135779110A>C	GRCh37
NC_000009.10:g.134768931A>C	NCBI36
NG_012386.1:g.45911T>G , LRG_486:g.45911T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2133T>G	ENSP00000496126.2:p.His711Gln
ENST00000490179.4:c.2136T>G	ENSP00000495533.2:p.His712Gln
ENST00000642261.2:c.2136T>G	ENSP00000494743.2:p.His712Gln
ENST00000643275.2:c.*76T>G	ENSP00000495598.2:n.*76T>G
ENST00000643362.2:c.1749T>G	ENSP00000496398.2:p.His583Gln
ENST00000643625.2:c.2041+688T>G	ENSP00000495546.2:n.2041+688T>G
ENST00000643691.2:c.1773T>G	ENSP00000494916.2:p.His591Gln
ENST00000644184.2:c.2136T>G	ENSP00000495428.2:p.His712Gln
ENST00000645129.2:c.1980T>G	ENSP00000493639.2:p.His660Gln
ENST00000646440.2:c.2136T>G	ENSP00000495830.2:p.His712Gln
ENST00000298552.9:c.2136T>G MANE Select	ENSP00000298552.3:p.His712Gln
ENST00000642261.1:c.200T>G
ENST00000642617.1:c.2133T>G	ENSP00000493773.1:p.His711Gln
ENST00000642627.1:c.2118T>G	ENSP00000496772.1:p.His706Gln
ENST00000642811.1:c.*1906T>G	ENSP00000495554.1:n.*1906T>G
ENST00000643072.1:c.1983T>G	ENSP00000496691.1:p.His661Gln
ENST00000643275.1:c.610T>G	ENSP00000495598.1:n.610T>G
ENST00000643583.1:c.2121T>G	ENSP00000494685.1:p.His707Gln
ENST00000643625.1:c.85+688T>G	ENSP00000495546.1:n.85+688T>G
ENST00000643875.1:c.2136T>G	ENSP00000495158.1:p.His712Gln
ENST00000644097.1:c.2133T>G	ENSP00000494682.1:p.His711Gln
ENST00000644184.1:c.873T>G	ENSP00000495428.1:p.His291Gln
ENST00000644255.1:c.*1903T>G	ENSP00000493608.1:n.*1903T>G
ENST00000644319.1:n.2511T>G
ENST00000644882.1:n.1091T>G
ENST00000645901.1:n.2987T>G
ENST00000646391.1:c.*1906T>G	ENSP00000494104.1:n.*1906T>G
ENST00000646625.1:c.2136T>G	ENSP00000496263.1:p.His712Gln
ENST00000647262.1:n.1101T>G
ENST00000647279.1:c.*1375T>G	ENSP00000494502.1:n.*1375T>G
ENST00000647506.1:n.3012T>G
ENST00000647534.1:n.1200T>G
ENST00000298552.7:c.2136T>G	ENSP00000298552.3:p.His712Gln
ENST00000440111.6:c.2136T>G	ENSP00000394524.2:p.His712Gln
ENST00000545250.5:c.1983T>G	ENSP00000444017.1:p.His661Gln
NM_000368.4:c.2136T>G , LRG_486t1:c.2136T>G	NP_000359.1:p.His712Gln
NM_001162426.1:c.2133T>G	NP_001155898.1:p.His711Gln
NM_001162427.1:c.1983T>G	NP_001155899.1:p.His661Gln
XM_005272211.1:c.2136T>G	XP_005272268.1:p.His712Gln
XM_006717271.1:c.2136T>G	XP_006717334.1:p.His712Gln
XM_011518979.1:c.2136T>G	XP_011517281.1:p.His712Gln
NM_001362177.1:c.1773T>G	NP_001349106.1:p.His591Gln
XM_011518979.2:c.2136T>G	XP_011517281.1:p.His712Gln
XM_017015096.1:c.2136T>G	XP_016870585.1:p.His712Gln
XM_017015097.1:c.2136T>G	XP_016870586.1:p.His712Gln
XM_017015098.1:c.2133T>G	XP_016870587.1:p.His711Gln
XM_017015100.1:c.1773T>G	XP_016870589.1:p.His591Gln
XM_017015101.1:c.1770T>G	XP_016870590.1:p.His590Gln
NM_000368.5:c.2136T>G MANE Select	NP_000359.1:p.His712Gln
NM_001162426.2:c.2133T>G	NP_001155898.1:p.His711Gln
NM_001162427.2:c.1983T>G	NP_001155899.1:p.His661Gln
NM_001362177.2:c.1773T>G	NP_001349106.1:p.His591Gln