Canonical Allele Identifier: CA375370055

Gene: TSC1

Linked Data

• COSMIC: COSM1757247
• MyVariant Identifiers: chr9:g.135776155C>G (hg19) ; chr9:g.132900768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900768C>G , CM000671.2:g.132900768C>G	GRCh38
NC_000009.11:g.135776155C>G , CM000671.1:g.135776155C>G	GRCh37
NC_000009.10:g.134765976C>G	NCBI36
NG_012386.1:g.48866G>C , LRG_486:g.48866G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2569G>C	ENSP00000496126.2:p.Val857Leu
ENST00000490179.4:c.2572G>C	ENSP00000495533.2:p.Val858Leu
ENST00000642261.2:c.*351G>C	ENSP00000494743.2:n.*351G>C
ENST00000643275.2:c.*512G>C	ENSP00000495598.2:n.*512G>C
ENST00000643362.2:c.2185G>C	ENSP00000496398.2:p.Val729Leu
ENST00000643625.2:c.*314G>C	ENSP00000495546.2:n.*314G>C
ENST00000643691.2:c.2209G>C	ENSP00000494916.2:p.Val737Leu
ENST00000644184.2:c.2530G>C	ENSP00000495428.2:p.Val844Leu
ENST00000645129.2:c.2416G>C	ENSP00000493639.2:p.Val806Leu
ENST00000646440.2:c.2572G>C	ENSP00000495830.2:p.Val858Leu
ENST00000298552.9:c.2572G>C MANE Select	ENSP00000298552.3:p.Val858Leu
ENST00000642261.1:c.632G>C
ENST00000642617.1:c.2569G>C	ENSP00000493773.1:p.Val857Leu
ENST00000642627.1:c.2554G>C	ENSP00000496772.1:p.Val852Leu
ENST00000642811.1:c.*2342G>C	ENSP00000495554.1:n.*2342G>C
ENST00000643072.1:c.2419G>C	ENSP00000496691.1:p.Val807Leu
ENST00000643275.1:c.1046G>C	ENSP00000495598.1:n.1046G>C
ENST00000643583.1:c.2557G>C	ENSP00000494685.1:p.Val853Leu
ENST00000643625.1:c.449G>C	ENSP00000495546.1:n.449G>C
ENST00000643875.1:c.2572G>C	ENSP00000495158.1:p.Val858Leu
ENST00000644097.1:c.2569G>C	ENSP00000494682.1:p.Val857Leu
ENST00000644184.1:c.1267G>C	ENSP00000495428.1:p.Val423Leu
ENST00000644255.1:c.*2339G>C	ENSP00000493608.1:n.*2339G>C
ENST00000644319.1:n.2947G>C
ENST00000644786.1:n.231G>C
ENST00000644882.1:n.1485G>C
ENST00000645901.1:n.3423G>C
ENST00000646391.1:c.*2342G>C	ENSP00000494104.1:n.*2342G>C
ENST00000646625.1:c.2572G>C	ENSP00000496263.1:p.Val858Leu
ENST00000647262.1:n.1537G>C
ENST00000647279.1:c.*1811G>C	ENSP00000494502.1:n.*1811G>C
ENST00000647506.1:n.3448G>C
ENST00000647534.1:n.1636G>C
ENST00000298552.7:c.2572G>C	ENSP00000298552.3:p.Val858Leu
ENST00000440111.6:c.2572G>C	ENSP00000394524.2:p.Val858Leu
ENST00000545250.5:c.2419G>C	ENSP00000444017.1:p.Val807Leu
NM_000368.4:c.2572G>C , LRG_486t1:c.2572G>C	NP_000359.1:p.Val858Leu
NM_001162426.1:c.2569G>C	NP_001155898.1:p.Val857Leu
NM_001162427.1:c.2419G>C	NP_001155899.1:p.Val807Leu
XM_005272211.1:c.2572G>C	XP_005272268.1:p.Val858Leu
XM_006717271.1:c.2572G>C	XP_006717334.1:p.Val858Leu
XM_011518979.1:c.2572G>C	XP_011517281.1:p.Val858Leu
NM_001362177.1:c.2209G>C	NP_001349106.1:p.Val737Leu
XM_011518979.2:c.2572G>C	XP_011517281.1:p.Val858Leu
XM_017015096.1:c.2572G>C	XP_016870585.1:p.Val858Leu
XM_017015097.1:c.2572G>C	XP_016870586.1:p.Val858Leu
XM_017015098.1:c.2569G>C	XP_016870587.1:p.Val857Leu
XM_017015100.1:c.2209G>C	XP_016870589.1:p.Val737Leu
XM_017015101.1:c.2206G>C	XP_016870590.1:p.Val736Leu
NM_000368.5:c.2572G>C MANE Select	NP_000359.1:p.Val858Leu
NM_001162426.2:c.2569G>C	NP_001155898.1:p.Val857Leu
NM_001162427.2:c.2419G>C	NP_001155899.1:p.Val807Leu
NM_001362177.2:c.2209G>C	NP_001349106.1:p.Val737Leu