Canonical Allele Identifier: CA005658

Gene: TSC1

Linked Data

• ClinVar Variation Id: 48858
• ClinVar RCV Id: RCV000042109 ; RCV000713908 ; RCV000698745 ; RCV002415486
• dbSNP Id: rs75820036
• MyVariant Identifiers: chr9:g.135781005G>A (hg19) ; chr9:g.132905618G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132905618G>A , CM000671.2:g.132905618G>A	GRCh38
NC_000009.11:g.135781005G>A , CM000671.1:g.135781005G>A	GRCh37
NC_000009.10:g.134770826G>A	NCBI36
NG_012386.1:g.44016C>T , LRG_486:g.44016C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1957C>T	ENSP00000496126.2:p.Gln653Ter
ENST00000490179.4:c.1960C>T	ENSP00000495533.2:p.Gln654Ter
ENST00000642261.2:c.1960C>T	ENSP00000494743.2:p.Gln654Ter
ENST00000643275.2:c.1960C>T	ENSP00000495598.2:p.Gln654Ter
ENST00000643362.2:c.1573C>T	ENSP00000496398.2:p.Gln525Ter
ENST00000643625.2:c.1960C>T	ENSP00000495546.2:p.Gln654Ter
ENST00000643691.2:c.1597C>T	ENSP00000494916.2:p.Gln533Ter
ENST00000644184.2:c.1960C>T	ENSP00000495428.2:p.Gln654Ter
ENST00000645129.2:c.1804C>T	ENSP00000493639.2:p.Gln602Ter
ENST00000646440.2:c.1960C>T	ENSP00000495830.2:p.Gln654Ter
ENST00000298552.9:c.1960C>T MANE Select	ENSP00000298552.3:p.Gln654Ter
ENST00000642261.1:c.24C>T
ENST00000642617.1:c.1957C>T	ENSP00000493773.1:p.Gln653Ter
ENST00000642627.1:c.1957C>T	ENSP00000496772.1:p.Gln653Ter
ENST00000642811.1:c.*1730C>T	ENSP00000495554.1:n.*1730C>T
ENST00000643072.1:c.1807C>T	ENSP00000496691.1:p.Gln603Ter
ENST00000643275.1:c.478C>T	ENSP00000495598.1:p.Gln160Ter
ENST00000643583.1:c.1960C>T	ENSP00000494685.1:p.Gln654Ter
ENST00000643625.1:c.4C>T	ENSP00000495546.1:p.Gln2Ter
ENST00000643875.1:c.1960C>T	ENSP00000495158.1:p.Gln654Ter
ENST00000644097.1:c.1957C>T	ENSP00000494682.1:p.Gln653Ter
ENST00000644184.1:c.697C>T	ENSP00000495428.1:p.Gln233Ter
ENST00000644255.1:c.*1727C>T	ENSP00000493608.1:n.*1727C>T
ENST00000644319.1:n.2335C>T
ENST00000644882.1:n.915C>T
ENST00000645901.1:n.2811C>T
ENST00000646391.1:c.*1730C>T	ENSP00000494104.1:n.*1730C>T
ENST00000646625.1:c.1960C>T	ENSP00000496263.1:p.Gln654Ter
ENST00000647262.1:n.925C>T
ENST00000647279.1:c.*1199C>T	ENSP00000494502.1:n.*1199C>T
ENST00000647506.1:n.2836C>T
ENST00000647534.1:n.1024C>T
ENST00000298552.7:c.1960C>T	ENSP00000298552.3:p.Gln654Ter
ENST00000440111.6:c.1960C>T	ENSP00000394524.2:p.Gln654Ter
ENST00000545250.5:c.1807C>T	ENSP00000444017.1:p.Gln603Ter
NM_000368.4:c.1960C>T , LRG_486t1:c.1960C>T	NP_000359.1:p.Gln654Ter
NM_001162426.1:c.1957C>T	NP_001155898.1:p.Gln653Ter
NM_001162427.1:c.1807C>T	NP_001155899.1:p.Gln603Ter
XM_005272211.1:c.1960C>T	XP_005272268.1:p.Gln654Ter
XM_006717271.1:c.1960C>T	XP_006717334.1:p.Gln654Ter
XM_006717272.2:c.1960C>T	XP_006717335.1:p.Gln654Ter
XM_011518979.1:c.1960C>T	XP_011517281.1:p.Gln654Ter
NM_001362177.1:c.1597C>T	NP_001349106.1:p.Gln533Ter
XM_011518979.2:c.1960C>T	XP_011517281.1:p.Gln654Ter
XM_017015096.1:c.1960C>T	XP_016870585.1:p.Gln654Ter
XM_017015097.1:c.1960C>T	XP_016870586.1:p.Gln654Ter
XM_017015098.1:c.1957C>T	XP_016870587.1:p.Gln653Ter
XM_017015100.1:c.1597C>T	XP_016870589.1:p.Gln533Ter
XM_017015101.1:c.1594C>T	XP_016870590.1:p.Gln532Ter
NM_000368.5:c.1960C>T MANE Select	NP_000359.1:p.Gln654Ter
NM_001162426.2:c.1957C>T	NP_001155898.1:p.Gln653Ter
NM_001162427.2:c.1807C>T	NP_001155899.1:p.Gln603Ter
NM_001362177.2:c.1597C>T	NP_001349106.1:p.Gln533Ter