Canonical Allele Identifier: CA375370308

Gene: TSC1

Linked Data

• MyVariant Identifiers: chr9:g.135776210C>G (hg19) ; chr9:g.132900823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900823C>G , CM000671.2:g.132900823C>G	GRCh38
NC_000009.11:g.135776210C>G , CM000671.1:g.135776210C>G	GRCh37
NC_000009.10:g.134766031C>G	NCBI36
NG_012386.1:g.48811G>C , LRG_486:g.48811G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2514G>C	ENSP00000496126.2:p.Glu838Asp
ENST00000490179.4:c.2517G>C	ENSP00000495533.2:p.Glu839Asp
ENST00000642261.2:c.*296G>C	ENSP00000494743.2:n.*296G>C
ENST00000643275.2:c.*457G>C	ENSP00000495598.2:n.*457G>C
ENST00000643362.2:c.2130G>C	ENSP00000496398.2:p.Glu710Asp
ENST00000643625.2:c.*259G>C	ENSP00000495546.2:n.*259G>C
ENST00000643691.2:c.2154G>C	ENSP00000494916.2:p.Glu718Asp
ENST00000644184.2:c.2475G>C	ENSP00000495428.2:p.Glu825Asp
ENST00000645129.2:c.2361G>C	ENSP00000493639.2:p.Glu787Asp
ENST00000646440.2:c.2517G>C	ENSP00000495830.2:p.Glu839Asp
ENST00000298552.9:c.2517G>C MANE Select	ENSP00000298552.3:p.Glu839Asp
ENST00000642261.1:c.577G>C
ENST00000642617.1:c.2514G>C	ENSP00000493773.1:p.Glu838Asp
ENST00000642627.1:c.2499G>C	ENSP00000496772.1:p.Glu833Asp
ENST00000642811.1:c.*2287G>C	ENSP00000495554.1:n.*2287G>C
ENST00000643072.1:c.2364G>C	ENSP00000496691.1:p.Glu788Asp
ENST00000643275.1:c.991G>C	ENSP00000495598.1:n.991G>C
ENST00000643583.1:c.2502G>C	ENSP00000494685.1:p.Glu834Asp
ENST00000643625.1:c.394G>C	ENSP00000495546.1:n.394G>C
ENST00000643875.1:c.2517G>C	ENSP00000495158.1:p.Glu839Asp
ENST00000644097.1:c.2514G>C	ENSP00000494682.1:p.Glu838Asp
ENST00000644184.1:c.1212G>C	ENSP00000495428.1:p.Glu404Asp
ENST00000644255.1:c.*2284G>C	ENSP00000493608.1:n.*2284G>C
ENST00000644319.1:n.2892G>C
ENST00000644786.1:n.176G>C
ENST00000644882.1:n.1430G>C
ENST00000645901.1:n.3368G>C
ENST00000646391.1:c.*2287G>C	ENSP00000494104.1:n.*2287G>C
ENST00000646625.1:c.2517G>C	ENSP00000496263.1:p.Glu839Asp
ENST00000647262.1:n.1482G>C
ENST00000647279.1:c.*1756G>C	ENSP00000494502.1:n.*1756G>C
ENST00000647506.1:n.3393G>C
ENST00000647534.1:n.1581G>C
ENST00000298552.7:c.2517G>C	ENSP00000298552.3:p.Glu839Asp
ENST00000440111.6:c.2517G>C	ENSP00000394524.2:p.Glu839Asp
ENST00000545250.5:c.2364G>C	ENSP00000444017.1:p.Glu788Asp
NM_000368.4:c.2517G>C , LRG_486t1:c.2517G>C	NP_000359.1:p.Glu839Asp
NM_001162426.1:c.2514G>C	NP_001155898.1:p.Glu838Asp
NM_001162427.1:c.2364G>C	NP_001155899.1:p.Glu788Asp
XM_005272211.1:c.2517G>C	XP_005272268.1:p.Glu839Asp
XM_006717271.1:c.2517G>C	XP_006717334.1:p.Glu839Asp
XM_011518979.1:c.2517G>C	XP_011517281.1:p.Glu839Asp
NM_001362177.1:c.2154G>C	NP_001349106.1:p.Glu718Asp
XM_011518979.2:c.2517G>C	XP_011517281.1:p.Glu839Asp
XM_017015096.1:c.2517G>C	XP_016870585.1:p.Glu839Asp
XM_017015097.1:c.2517G>C	XP_016870586.1:p.Glu839Asp
XM_017015098.1:c.2514G>C	XP_016870587.1:p.Glu838Asp
XM_017015100.1:c.2154G>C	XP_016870589.1:p.Glu718Asp
XM_017015101.1:c.2151G>C	XP_016870590.1:p.Glu717Asp
NM_000368.5:c.2517G>C MANE Select	NP_000359.1:p.Glu839Asp
NM_001162426.2:c.2514G>C	NP_001155898.1:p.Glu838Asp
NM_001162427.2:c.2364G>C	NP_001155899.1:p.Glu788Asp
NM_001362177.2:c.2154G>C	NP_001349106.1:p.Glu718Asp