Canonical Allele Identifier: CA375363130

Gene: TSC1

Linked Data

• dbSNP Id: rs2131818558
• MyVariant Identifiers: chr9:g.135781112T>A (hg19) ; chr9:g.132905725T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132905725T>A , CM000671.2:g.132905725T>A	GRCh38
NC_000009.11:g.135781112T>A , CM000671.1:g.135781112T>A	GRCh37
NC_000009.10:g.134770933T>A	NCBI36
NG_012386.1:g.43909A>T , LRG_486:g.43909A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.1850A>T	ENSP00000496126.2:p.His617Leu
ENST00000490179.4:c.1853A>T	ENSP00000495533.2:p.His618Leu
ENST00000642261.2:c.1853A>T	ENSP00000494743.2:p.His618Leu
ENST00000643275.2:c.1853A>T	ENSP00000495598.2:p.His618Leu
ENST00000643362.2:c.1466A>T	ENSP00000496398.2:p.His489Leu
ENST00000643625.2:c.1853A>T	ENSP00000495546.2:p.His618Leu
ENST00000643691.2:c.1490A>T	ENSP00000494916.2:p.His497Leu
ENST00000644184.2:c.1853A>T	ENSP00000495428.2:p.His618Leu
ENST00000645129.2:c.1697A>T	ENSP00000493639.2:p.His566Leu
ENST00000646440.2:c.1853A>T	ENSP00000495830.2:p.His618Leu
ENST00000298552.9:c.1853A>T MANE Select	ENSP00000298552.3:p.His618Leu
ENST00000642617.1:c.1850A>T	ENSP00000493773.1:p.His617Leu
ENST00000642627.1:c.1850A>T	ENSP00000496772.1:p.His617Leu
ENST00000642811.1:c.*1623A>T	ENSP00000495554.1:n.*1623A>T
ENST00000643072.1:c.1700A>T	ENSP00000496691.1:p.His567Leu
ENST00000643275.1:c.371A>T	ENSP00000495598.1:p.His124Leu
ENST00000643583.1:c.1853A>T	ENSP00000494685.1:p.His618Leu
ENST00000643875.1:c.1853A>T	ENSP00000495158.1:p.His618Leu
ENST00000644097.1:c.1850A>T	ENSP00000494682.1:p.His617Leu
ENST00000644184.1:c.590A>T	ENSP00000495428.1:p.His197Leu
ENST00000644255.1:c.*1620A>T	ENSP00000493608.1:n.*1620A>T
ENST00000644319.1:n.2228A>T
ENST00000644882.1:n.808A>T
ENST00000645901.1:n.2704A>T
ENST00000646391.1:c.*1623A>T	ENSP00000494104.1:n.*1623A>T
ENST00000646625.1:c.1853A>T	ENSP00000496263.1:p.His618Leu
ENST00000647262.1:n.818A>T
ENST00000647279.1:c.*1092A>T	ENSP00000494502.1:n.*1092A>T
ENST00000647506.1:n.2729A>T
ENST00000647534.1:n.917A>T
ENST00000298552.7:c.1853A>T	ENSP00000298552.3:p.His618Leu
ENST00000440111.6:c.1853A>T	ENSP00000394524.2:p.His618Leu
ENST00000545250.5:c.1700A>T	ENSP00000444017.1:p.His567Leu
NM_000368.4:c.1853A>T , LRG_486t1:c.1853A>T	NP_000359.1:p.His618Leu
NM_001162426.1:c.1850A>T	NP_001155898.1:p.His617Leu
NM_001162427.1:c.1700A>T	NP_001155899.1:p.His567Leu
XM_005272211.1:c.1853A>T	XP_005272268.1:p.His618Leu
XM_006717271.1:c.1853A>T	XP_006717334.1:p.His618Leu
XM_006717272.2:c.1853A>T	XP_006717335.1:p.His618Leu
XM_011518979.1:c.1853A>T	XP_011517281.1:p.His618Leu
NM_001362177.1:c.1490A>T	NP_001349106.1:p.His497Leu
XM_011518979.2:c.1853A>T	XP_011517281.1:p.His618Leu
XM_017015096.1:c.1853A>T	XP_016870585.1:p.His618Leu
XM_017015097.1:c.1853A>T	XP_016870586.1:p.His618Leu
XM_017015098.1:c.1850A>T	XP_016870587.1:p.His617Leu
XM_017015100.1:c.1490A>T	XP_016870589.1:p.His497Leu
XM_017015101.1:c.1487A>T	XP_016870590.1:p.His496Leu
NM_000368.5:c.1853A>T MANE Select	NP_000359.1:p.His618Leu
NM_001162426.2:c.1850A>T	NP_001155898.1:p.His617Leu
NM_001162427.2:c.1700A>T	NP_001155899.1:p.His567Leu
NM_001362177.2:c.1490A>T	NP_001349106.1:p.His497Leu