Canonical Allele Identifier: CA006274

Gene: TSC1

Linked Data

• ClinVar Variation Id: 48936
• ClinVar RCV Id: RCV000042187 ; RCV003915004
• dbSNP Id: rs118203675
• MyVariant Identifiers: chr9:g.135778084G>A (hg19) ; chr9:g.132902697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132902697G>A , CM000671.2:g.132902697G>A	GRCh38
NC_000009.11:g.135778084G>A , CM000671.1:g.135778084G>A	GRCh37
NC_000009.10:g.134767905G>A	NCBI36
NG_012386.1:g.46937C>T , LRG_486:g.46937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2296C>T	ENSP00000496126.2:p.Gln766Ter
ENST00000490179.4:c.2299C>T	ENSP00000495533.2:p.Gln767Ter
ENST00000642261.2:c.*78C>T	ENSP00000494743.2:n.*78C>T
ENST00000643275.2:c.*239C>T	ENSP00000495598.2:n.*239C>T
ENST00000643362.2:c.1912C>T	ENSP00000496398.2:p.Gln638Ter
ENST00000643625.2:c.*41C>T	ENSP00000495546.2:n.*41C>T
ENST00000643691.2:c.1936C>T	ENSP00000494916.2:p.Gln646Ter
ENST00000644184.2:c.2299C>T	ENSP00000495428.2:p.Gln767Ter
ENST00000645129.2:c.2143C>T	ENSP00000493639.2:p.Gln715Ter
ENST00000646440.2:c.2299C>T	ENSP00000495830.2:p.Gln767Ter
ENST00000298552.9:c.2299C>T MANE Select	ENSP00000298552.3:p.Gln767Ter
ENST00000642261.1:c.359C>T
ENST00000642617.1:c.2296C>T	ENSP00000493773.1:p.Gln766Ter
ENST00000642627.1:c.2281C>T	ENSP00000496772.1:p.Gln761Ter
ENST00000642811.1:c.*2069C>T	ENSP00000495554.1:n.*2069C>T
ENST00000643072.1:c.2146C>T	ENSP00000496691.1:p.Gln716Ter
ENST00000643275.1:c.773C>T	ENSP00000495598.1:n.773C>T
ENST00000643583.1:c.2284C>T	ENSP00000494685.1:p.Gln762Ter
ENST00000643625.1:c.176C>T	ENSP00000495546.1:n.176C>T
ENST00000643875.1:c.2299C>T	ENSP00000495158.1:p.Gln767Ter
ENST00000644097.1:c.2296C>T	ENSP00000494682.1:p.Gln766Ter
ENST00000644184.1:c.1036C>T	ENSP00000495428.1:p.Gln346Ter
ENST00000644255.1:c.*2066C>T	ENSP00000493608.1:n.*2066C>T
ENST00000644319.1:n.2674C>T
ENST00000644882.1:n.1254C>T
ENST00000645901.1:n.3150C>T
ENST00000646391.1:c.*2069C>T	ENSP00000494104.1:n.*2069C>T
ENST00000646625.1:c.2299C>T	ENSP00000496263.1:p.Gln767Ter
ENST00000647262.1:n.1264C>T
ENST00000647279.1:c.*1538C>T	ENSP00000494502.1:n.*1538C>T
ENST00000647506.1:n.3175C>T
ENST00000647534.1:n.1363C>T
ENST00000298552.7:c.2299C>T	ENSP00000298552.3:p.Gln767Ter
ENST00000440111.6:c.2299C>T	ENSP00000394524.2:p.Gln767Ter
ENST00000545250.5:c.2146C>T	ENSP00000444017.1:p.Gln716Ter
NM_000368.4:c.2299C>T , LRG_486t1:c.2299C>T	NP_000359.1:p.Gln767Ter
NM_001162426.1:c.2296C>T	NP_001155898.1:p.Gln766Ter
NM_001162427.1:c.2146C>T	NP_001155899.1:p.Gln716Ter
XM_005272211.1:c.2299C>T	XP_005272268.1:p.Gln767Ter
XM_006717271.1:c.2299C>T	XP_006717334.1:p.Gln767Ter
XM_011518979.1:c.2299C>T	XP_011517281.1:p.Gln767Ter
NM_001362177.1:c.1936C>T	NP_001349106.1:p.Gln646Ter
XM_011518979.2:c.2299C>T	XP_011517281.1:p.Gln767Ter
XM_017015096.1:c.2299C>T	XP_016870585.1:p.Gln767Ter
XM_017015097.1:c.2299C>T	XP_016870586.1:p.Gln767Ter
XM_017015098.1:c.2296C>T	XP_016870587.1:p.Gln766Ter
XM_017015100.1:c.1936C>T	XP_016870589.1:p.Gln646Ter
XM_017015101.1:c.1933C>T	XP_016870590.1:p.Gln645Ter
NM_000368.5:c.2299C>T MANE Select	NP_000359.1:p.Gln767Ter
NM_001162426.2:c.2296C>T	NP_001155898.1:p.Gln766Ter
NM_001162427.2:c.2146C>T	NP_001155899.1:p.Gln716Ter
NM_001362177.2:c.1936C>T	NP_001349106.1:p.Gln646Ter