Canonical Allele Identifier: CA375360112

Gene: TSC1

Linked Data

• dbSNP Id: rs1186305034
• MyVariant Identifiers: chr9:g.135778166C>G (hg19) ; chr9:g.132902779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132902779C>G , CM000671.2:g.132902779C>G	GRCh38
NC_000009.11:g.135778166C>G , CM000671.1:g.135778166C>G	GRCh37
NC_000009.10:g.134767987C>G	NCBI36
NG_012386.1:g.46855G>C , LRG_486:g.46855G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2214G>C	ENSP00000496126.2:p.Gln738His
ENST00000490179.4:c.2217G>C	ENSP00000495533.2:p.Gln739His
ENST00000642261.2:c.2213G>C	ENSP00000494743.2:p.Ser738Thr
ENST00000643275.2:c.*157G>C	ENSP00000495598.2:n.*157G>C
ENST00000643362.2:c.1830G>C	ENSP00000496398.2:p.Gln610His
ENST00000643625.2:c.2050G>C	ENSP00000495546.2:p.Val684Leu
ENST00000643691.2:c.1854G>C	ENSP00000494916.2:p.Gln618His
ENST00000644184.2:c.2217G>C	ENSP00000495428.2:p.Gln739His
ENST00000645129.2:c.2061G>C	ENSP00000493639.2:p.Gln687His
ENST00000646440.2:c.2217G>C	ENSP00000495830.2:p.Gln739His
ENST00000298552.9:c.2217G>C MANE Select	ENSP00000298552.3:p.Gln739His
ENST00000642261.1:c.277G>C
ENST00000642617.1:c.2214G>C	ENSP00000493773.1:p.Gln738His
ENST00000642627.1:c.2199G>C	ENSP00000496772.1:p.Gln733His
ENST00000642811.1:c.*1987G>C	ENSP00000495554.1:n.*1987G>C
ENST00000643072.1:c.2064G>C	ENSP00000496691.1:p.Gln688His
ENST00000643275.1:c.691G>C	ENSP00000495598.1:n.691G>C
ENST00000643583.1:c.2202G>C	ENSP00000494685.1:p.Gln734His
ENST00000643625.1:c.94G>C	ENSP00000495546.1:p.Val32Leu
ENST00000643875.1:c.2217G>C	ENSP00000495158.1:p.Gln739His
ENST00000644097.1:c.2214G>C	ENSP00000494682.1:p.Gln738His
ENST00000644184.1:c.954G>C	ENSP00000495428.1:p.Gln318His
ENST00000644255.1:c.*1984G>C	ENSP00000493608.1:n.*1984G>C
ENST00000644319.1:n.2592G>C
ENST00000644882.1:n.1172G>C
ENST00000645901.1:n.3068G>C
ENST00000646391.1:c.*1987G>C	ENSP00000494104.1:n.*1987G>C
ENST00000646625.1:c.2217G>C	ENSP00000496263.1:p.Gln739His
ENST00000647262.1:n.1182G>C
ENST00000647279.1:c.*1456G>C	ENSP00000494502.1:n.*1456G>C
ENST00000647506.1:n.3093G>C
ENST00000647534.1:n.1281G>C
ENST00000298552.7:c.2217G>C	ENSP00000298552.3:p.Gln739His
ENST00000440111.6:c.2217G>C	ENSP00000394524.2:p.Gln739His
ENST00000545250.5:c.2064G>C	ENSP00000444017.1:p.Gln688His
NM_000368.4:c.2217G>C , LRG_486t1:c.2217G>C	NP_000359.1:p.Gln739His
NM_001162426.1:c.2214G>C	NP_001155898.1:p.Gln738His
NM_001162427.1:c.2064G>C	NP_001155899.1:p.Gln688His
XM_005272211.1:c.2217G>C	XP_005272268.1:p.Gln739His
XM_006717271.1:c.2217G>C	XP_006717334.1:p.Gln739His
XM_011518979.1:c.2217G>C	XP_011517281.1:p.Gln739His
NM_001362177.1:c.1854G>C	NP_001349106.1:p.Gln618His
XM_011518979.2:c.2217G>C	XP_011517281.1:p.Gln739His
XM_017015096.1:c.2217G>C	XP_016870585.1:p.Gln739His
XM_017015097.1:c.2217G>C	XP_016870586.1:p.Gln739His
XM_017015098.1:c.2214G>C	XP_016870587.1:p.Gln738His
XM_017015100.1:c.1854G>C	XP_016870589.1:p.Gln618His
XM_017015101.1:c.1851G>C	XP_016870590.1:p.Gln617His
NM_000368.5:c.2217G>C MANE Select	NP_000359.1:p.Gln739His
NM_001162426.2:c.2214G>C	NP_001155898.1:p.Gln738His
NM_001162427.2:c.2064G>C	NP_001155899.1:p.Gln688His
NM_001362177.2:c.1854G>C	NP_001349106.1:p.Gln618His