Canonical Allele Identifier: CA039098

Gene: TSC1

Linked Data

• ClinVar Variation Id: 237728
• ClinVar RCV Id: RCV000227461 ; RCV000270939 ; RCV000566627 ; RCV003998781
• dbSNP Id: rs148756522
• ExAC: 9:135787763 A / C
• gnomAD v2: 9-135787763-A-C
• gnomAD v3: 9-132912376-A-C
• gnomAD v4: 9-132912376-A-C
• MyVariant Identifiers: chr9:g.135787763A>C (hg19) ; chr9:g.132912376A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132912376A>C , CM000671.2:g.132912376A>C	GRCh38
NC_000009.11:g.135787763A>C , CM000671.1:g.135787763A>C	GRCh37
NC_000009.10:g.134777584A>C	NCBI36
NG_012386.1:g.37258T>G , LRG_486:g.37258T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.819T>G	ENSP00000496126.2:p.Asp273Glu
ENST00000490179.4:c.819T>G	ENSP00000495533.2:p.Asp273Glu
ENST00000642261.2:c.819T>G	ENSP00000494743.2:p.Asp273Glu
ENST00000643275.2:c.819T>G	ENSP00000495598.2:p.Asp273Glu
ENST00000643362.2:c.666T>G	ENSP00000496398.2:p.Asp222Glu
ENST00000643625.2:c.819T>G	ENSP00000495546.2:p.Asp273Glu
ENST00000643691.2:c.456T>G	ENSP00000494916.2:p.Asp152Glu
ENST00000644184.2:c.819T>G	ENSP00000495428.2:p.Asp273Glu
ENST00000645129.2:c.666T>G	ENSP00000493639.2:p.Asp222Glu
ENST00000646440.2:c.819T>G	ENSP00000495830.2:p.Asp273Glu
ENST00000647078.2:c.819T>G	ENSP00000496066.1:p.Asp273Glu
ENST00000298552.9:c.819T>G MANE Select	ENSP00000298552.3:p.Asp273Glu
ENST00000403810.6:c.819T>G	ENSP00000386093.1:p.Asp273Glu
ENST00000493467.6:n.93T>G
ENST00000642344.1:c.*560T>G	ENSP00000494847.1:n.*560T>G
ENST00000642617.1:c.819T>G	ENSP00000493773.1:p.Asp273Glu
ENST00000642627.1:c.819T>G	ENSP00000496772.1:p.Asp273Glu
ENST00000642646.1:c.819T>G	ENSP00000496292.1:p.Asp273Glu
ENST00000642745.1:c.819T>G	ENSP00000493963.1:p.Asp273Glu
ENST00000642811.1:c.*589T>G	ENSP00000495554.1:n.*589T>G
ENST00000642854.1:c.*604T>G	ENSP00000494639.1:n.*604T>G
ENST00000643072.1:c.666T>G	ENSP00000496691.1:p.Asp222Glu
ENST00000643362.1:c.666T>G	ENSP00000496398.1:p.Asp222Glu
ENST00000643583.1:c.819T>G	ENSP00000494685.1:p.Asp273Glu
ENST00000643691.1:c.456T>G	ENSP00000494916.1:p.Asp152Glu
ENST00000643875.1:c.819T>G	ENSP00000495158.1:p.Asp273Glu
ENST00000644097.1:c.819T>G	ENSP00000494682.1:p.Asp273Glu
ENST00000644255.1:c.*589T>G	ENSP00000493608.1:n.*589T>G
ENST00000644319.1:n.546T>G
ENST00000644997.1:c.*476T>G	ENSP00000495654.1:n.*476T>G
ENST00000645129.1:c.666T>G	ENSP00000493639.1:p.Asp222Glu
ENST00000645150.1:c.819T>G	ENSP00000494365.1:p.Asp273Glu
ENST00000645901.1:n.1022T>G
ENST00000646391.1:c.*589T>G	ENSP00000494104.1:n.*589T>G
ENST00000646625.1:c.819T>G	ENSP00000496263.1:p.Asp273Glu
ENST00000647078.1:c.819T>G	ENSP00000496066.1:p.Asp273Glu
ENST00000647279.1:c.*58T>G	ENSP00000494502.1:n.*58T>G
ENST00000647462.1:c.819T>G	ENSP00000495821.1:p.Asp273Glu
ENST00000647506.1:n.1047T>G
ENST00000298552.7:c.819T>G	ENSP00000298552.3:p.Asp273Glu
ENST00000403810.5:c.819T>G	ENSP00000386093.1:p.Asp273Glu
ENST00000440111.6:c.819T>G	ENSP00000394524.2:p.Asp273Glu
ENST00000493467.5:n.1015T>G
ENST00000545250.5:c.666T>G	ENSP00000444017.1:p.Asp222Glu
NM_000368.4:c.819T>G , LRG_486t1:c.819T>G	NP_000359.1:p.Asp273Glu
NM_001162426.1:c.819T>G	NP_001155898.1:p.Asp273Glu
NM_001162427.1:c.666T>G	NP_001155899.1:p.Asp222Glu
XM_005272211.1:c.819T>G	XP_005272268.1:p.Asp273Glu
XM_006717271.1:c.819T>G	XP_006717334.1:p.Asp273Glu
XM_006717272.2:c.819T>G	XP_006717335.1:p.Asp273Glu
XM_011518979.1:c.819T>G	XP_011517281.1:p.Asp273Glu
NM_001362177.1:c.456T>G	NP_001349106.1:p.Asp152Glu
XM_011518979.2:c.819T>G	XP_011517281.1:p.Asp273Glu
XM_017015096.1:c.819T>G	XP_016870585.1:p.Asp273Glu
XM_017015097.1:c.819T>G	XP_016870586.1:p.Asp273Glu
XM_017015098.1:c.819T>G	XP_016870587.1:p.Asp273Glu
XM_017015100.1:c.456T>G	XP_016870589.1:p.Asp152Glu
XM_017015101.1:c.456T>G	XP_016870590.1:p.Asp152Glu
NM_000368.5:c.819T>G MANE Select	NP_000359.1:p.Asp273Glu
NM_001162426.2:c.819T>G	NP_001155898.1:p.Asp273Glu
NM_001162427.2:c.666T>G	NP_001155899.1:p.Asp222Glu
NM_001362177.2:c.456T>G	NP_001349106.1:p.Asp152Glu