Canonical Allele Identifier: CA005069

Gene: TSC1

Linked Data

• ClinVar Variation Id: 48804
• ClinVar RCV Id: RCV000042051 ; RCV000054972 ; RCV000578889 ; RCV000660336
• dbSNP Id: rs118203549
• MyVariant Identifiers: chr9:g.135781386G>A (hg19) ; chr9:g.132905999G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132905999G>A , CM000671.2:g.132905999G>A	GRCh38
NC_000009.11:g.135781386G>A , CM000671.1:g.135781386G>A	GRCh37
NC_000009.10:g.134771207G>A	NCBI36
NG_012386.1:g.43635C>T , LRG_486:g.43635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1576C>T	ENSP00000496126.2:p.Gln526Ter
ENST00000490179.4:c.1579C>T	ENSP00000495533.2:p.Gln527Ter
ENST00000642261.2:c.1579C>T	ENSP00000494743.2:p.Gln527Ter
ENST00000643275.2:c.1579C>T	ENSP00000495598.2:p.Gln527Ter
ENST00000643362.2:c.1192C>T	ENSP00000496398.2:p.Gln398Ter
ENST00000643625.2:c.1579C>T	ENSP00000495546.2:p.Gln527Ter
ENST00000643691.2:c.1216C>T	ENSP00000494916.2:p.Gln406Ter
ENST00000644184.2:c.1579C>T	ENSP00000495428.2:p.Gln527Ter
ENST00000645129.2:c.1423C>T	ENSP00000493639.2:p.Gln475Ter
ENST00000646440.2:c.1579C>T	ENSP00000495830.2:p.Gln527Ter
ENST00000298552.9:c.1579C>T MANE Select	ENSP00000298552.3:p.Gln527Ter
ENST00000642617.1:c.1576C>T	ENSP00000493773.1:p.Gln526Ter
ENST00000642627.1:c.1576C>T	ENSP00000496772.1:p.Gln526Ter
ENST00000642811.1:c.*1349C>T	ENSP00000495554.1:n.*1349C>T
ENST00000643072.1:c.1426C>T	ENSP00000496691.1:p.Gln476Ter
ENST00000643275.1:c.97C>T	ENSP00000495598.1:p.Gln33Ter
ENST00000643583.1:c.1579C>T	ENSP00000494685.1:p.Gln527Ter
ENST00000643875.1:c.1579C>T	ENSP00000495158.1:p.Gln527Ter
ENST00000644097.1:c.1576C>T	ENSP00000494682.1:p.Gln526Ter
ENST00000644184.1:c.316C>T	ENSP00000495428.1:p.Gln106Ter
ENST00000644255.1:c.*1346C>T	ENSP00000493608.1:n.*1346C>T
ENST00000644319.1:n.1954C>T
ENST00000644882.1:n.534C>T
ENST00000645901.1:n.2430C>T
ENST00000646391.1:c.*1349C>T	ENSP00000494104.1:n.*1349C>T
ENST00000646625.1:c.1579C>T	ENSP00000496263.1:p.Gln527Ter
ENST00000647262.1:n.544C>T
ENST00000647279.1:c.*818C>T	ENSP00000494502.1:n.*818C>T
ENST00000647506.1:n.2455C>T
ENST00000647534.1:n.643C>T
ENST00000298552.7:c.1579C>T	ENSP00000298552.3:p.Gln527Ter
ENST00000440111.6:c.1579C>T	ENSP00000394524.2:p.Gln527Ter
ENST00000545250.5:c.1426C>T	ENSP00000444017.1:p.Gln476Ter
NM_000368.4:c.1579C>T , LRG_486t1:c.1579C>T	NP_000359.1:p.Gln527Ter
NM_001162426.1:c.1576C>T	NP_001155898.1:p.Gln526Ter
NM_001162427.1:c.1426C>T	NP_001155899.1:p.Gln476Ter
XM_005272211.1:c.1579C>T	XP_005272268.1:p.Gln527Ter
XM_006717271.1:c.1579C>T	XP_006717334.1:p.Gln527Ter
XM_006717272.2:c.1579C>T	XP_006717335.1:p.Gln527Ter
XM_011518979.1:c.1579C>T	XP_011517281.1:p.Gln527Ter
NM_001362177.1:c.1216C>T	NP_001349106.1:p.Gln406Ter
XM_011518979.2:c.1579C>T	XP_011517281.1:p.Gln527Ter
XM_017015096.1:c.1579C>T	XP_016870585.1:p.Gln527Ter
XM_017015097.1:c.1579C>T	XP_016870586.1:p.Gln527Ter
XM_017015098.1:c.1576C>T	XP_016870587.1:p.Gln526Ter
XM_017015100.1:c.1216C>T	XP_016870589.1:p.Gln406Ter
XM_017015101.1:c.1213C>T	XP_016870590.1:p.Gln405Ter
NM_000368.5:c.1579C>T MANE Select	NP_000359.1:p.Gln527Ter
NM_001162426.2:c.1576C>T	NP_001155898.1:p.Gln526Ter
NM_001162427.2:c.1426C>T	NP_001155899.1:p.Gln476Ter
NM_001362177.2:c.1216C>T	NP_001349106.1:p.Gln406Ter