Canonical Allele Identifier: CA2697558141

Gene: TSC1

Linked Data

• ClinVar Variation Id: 2756267
• ClinVar RCV Id: RCV003504888

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903702_132903704del , CM000671.2:g.132903702_132903704del	GRCh38
NC_000009.11:g.135779089_135779091del , CM000671.1:g.135779089_135779091del	GRCh37
NC_000009.10:g.134768910_134768912del	NCBI36
NG_012386.1:g.45934_45936del , LRG_486:g.45934_45936del

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2156_2158del	ENSP00000496126.2:p.Leu719del
ENST00000490179.4:c.2159_2161del	ENSP00000495533.2:p.Leu720del
ENST00000642261.2:c.2159_2161del	ENSP00000494743.2:p.Leu720del
ENST00000643275.2:c.*99_*101del	ENSP00000495598.2:n.*99_*101del
ENST00000643362.2:c.1772_1774del	ENSP00000496398.2:p.Leu591del
ENST00000643625.2:c.2041+711_2041+713del	ENSP00000495546.2:n.2041+711_2041+713del
ENST00000643691.2:c.1796_1798del	ENSP00000494916.2:p.Leu599del
ENST00000644184.2:c.2159_2161del	ENSP00000495428.2:p.Leu720del
ENST00000645129.2:c.2003_2005del	ENSP00000493639.2:p.Leu668del
ENST00000646440.2:c.2159_2161del	ENSP00000495830.2:p.Leu720del
ENST00000298552.9:c.2159_2161del MANE Select	ENSP00000298552.3:p.Leu720del
ENST00000642261.1:c.223_225del
ENST00000642617.1:c.2156_2158del	ENSP00000493773.1:p.Leu719del
ENST00000642627.1:c.2141_2143del	ENSP00000496772.1:p.Leu714del
ENST00000642811.1:c.*1929_*1931del	ENSP00000495554.1:n.*1929_*1931del
ENST00000643072.1:c.2006_2008del	ENSP00000496691.1:p.Leu669del
ENST00000643275.1:c.633_635del	ENSP00000495598.1:n.633_635del
ENST00000643583.1:c.2144_2146del	ENSP00000494685.1:p.Leu715del
ENST00000643625.1:c.85+711_85+713del	ENSP00000495546.1:n.85+711_85+713del
ENST00000643875.1:c.2159_2161del	ENSP00000495158.1:p.Leu720del
ENST00000644097.1:c.2156_2158del	ENSP00000494682.1:p.Leu719del
ENST00000644184.1:c.896_898del	ENSP00000495428.1:p.Leu299del
ENST00000644255.1:c.*1926_*1928del	ENSP00000493608.1:n.*1926_*1928del
ENST00000644319.1:n.2534_2536del
ENST00000644882.1:n.1114_1116del
ENST00000645901.1:n.3010_3012del
ENST00000646391.1:c.*1929_*1931del	ENSP00000494104.1:n.*1929_*1931del
ENST00000646625.1:c.2159_2161del	ENSP00000496263.1:p.Leu720del
ENST00000647262.1:n.1124_1126del
ENST00000647279.1:c.*1398_*1400del	ENSP00000494502.1:n.*1398_*1400del
ENST00000647506.1:n.3035_3037del
ENST00000647534.1:n.1223_1225del
ENST00000298552.7:c.2159_2161del	ENSP00000298552.3:p.Leu720del
ENST00000440111.6:c.2159_2161del	ENSP00000394524.2:p.Leu720del
ENST00000545250.5:c.2006_2008del	ENSP00000444017.1:p.Leu669del
NM_000368.4:c.2159_2161del , LRG_486t1:c.2159_2161del	NP_000359.1:p.Leu720del
NM_001162426.1:c.2156_2158del	NP_001155898.1:p.Leu719del
NM_001162427.1:c.2006_2008del	NP_001155899.1:p.Leu669del
XM_005272211.1:c.2159_2161del	XP_005272268.1:p.Leu720del
XM_006717271.1:c.2159_2161del	XP_006717334.1:p.Leu720del
XM_011518979.1:c.2159_2161del	XP_011517281.1:p.Leu720del
NM_001362177.1:c.1796_1798del	NP_001349106.1:p.Leu599del
XM_011518979.2:c.2159_2161del	XP_011517281.1:p.Leu720del
XM_017015096.1:c.2159_2161del	XP_016870585.1:p.Leu720del
XM_017015097.1:c.2159_2161del	XP_016870586.1:p.Leu720del
XM_017015098.1:c.2156_2158del	XP_016870587.1:p.Leu719del
XM_017015100.1:c.1796_1798del	XP_016870589.1:p.Leu599del
XM_017015101.1:c.1793_1795del	XP_016870590.1:p.Leu598del
NM_000368.5:c.2159_2161del MANE Select	NP_000359.1:p.Leu720del
NM_001162426.2:c.2156_2158del	NP_001155898.1:p.Leu719del
NM_001162427.2:c.2006_2008del	NP_001155899.1:p.Leu669del
NM_001362177.2:c.1796_1798del	NP_001349106.1:p.Leu599del