Canonical Allele Identifier: CA375366947

Gene: TSC1

Linked Data

• ClinVar Variation Id: 534465
• ClinVar RCV Id: RCV000642033
• dbSNP Id: rs118203504
• MyVariant Identifiers: chr9:g.135786013G>T (hg19) ; chr9:g.132910626G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132910626G>T , CM000671.2:g.132910626G>T	GRCh38
NC_000009.11:g.135786013G>T , CM000671.1:g.135786013G>T	GRCh37
NC_000009.10:g.134775834G>T	NCBI36
NG_012386.1:g.39008C>A , LRG_486:g.39008C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1205C>A	ENSP00000496126.2:p.Ser402Ter
ENST00000490179.4:c.1208C>A	ENSP00000495533.2:p.Ser403Ter
ENST00000642261.2:c.1208C>A	ENSP00000494743.2:p.Ser403Ter
ENST00000643275.2:c.1208C>A	ENSP00000495598.2:p.Ser403Ter
ENST00000643362.2:c.876+827C>A	ENSP00000496398.2:n.876+827C>A
ENST00000643625.2:c.1208C>A	ENSP00000495546.2:p.Ser403Ter
ENST00000643691.2:c.845C>A	ENSP00000494916.2:p.Ser282Ter
ENST00000644184.2:c.1208C>A	ENSP00000495428.2:p.Ser403Ter
ENST00000645129.2:c.1052C>A	ENSP00000493639.2:p.Ser351Ter
ENST00000646440.2:c.1208C>A	ENSP00000495830.2:p.Ser403Ter
ENST00000647078.2:c.*102C>A	ENSP00000496066.1:n.*102C>A
ENST00000298552.9:c.1208C>A MANE Select	ENSP00000298552.3:p.Ser403Ter
ENST00000493467.6:n.479C>A
ENST00000642344.1:c.*949C>A	ENSP00000494847.1:n.*949C>A
ENST00000642617.1:c.1205C>A	ENSP00000493773.1:p.Ser402Ter
ENST00000642627.1:c.1205C>A	ENSP00000496772.1:p.Ser402Ter
ENST00000642646.1:c.1208C>A	ENSP00000496292.1:p.Ser403Ter
ENST00000642745.1:c.1208C>A	ENSP00000493963.1:p.Ser403Ter
ENST00000642811.1:c.*978C>A	ENSP00000495554.1:n.*978C>A
ENST00000643072.1:c.1055C>A	ENSP00000496691.1:p.Ser352Ter
ENST00000643362.1:c.876+827C>A	ENSP00000496398.1:n.876+827C>A
ENST00000643583.1:c.1208C>A	ENSP00000494685.1:p.Ser403Ter
ENST00000643875.1:c.1208C>A	ENSP00000495158.1:p.Ser403Ter
ENST00000644097.1:c.1205C>A	ENSP00000494682.1:p.Ser402Ter
ENST00000644255.1:c.*975C>A	ENSP00000493608.1:n.*975C>A
ENST00000644319.1:n.1583C>A
ENST00000644997.1:c.*862C>A	ENSP00000495654.1:n.*862C>A
ENST00000645150.1:c.1208C>A	ENSP00000494365.1:p.Ser403Ter
ENST00000645901.1:n.2059C>A
ENST00000646391.1:c.*978C>A	ENSP00000494104.1:n.*978C>A
ENST00000646625.1:c.1208C>A	ENSP00000496263.1:p.Ser403Ter
ENST00000647078.1:c.*102C>A	ENSP00000496066.1:n.*102C>A
ENST00000647279.1:c.*447C>A	ENSP00000494502.1:n.*447C>A
ENST00000647462.1:c.1205C>A	ENSP00000495821.1:p.Ser402Ter
ENST00000647506.1:n.2084C>A
ENST00000647534.1:n.272C>A
ENST00000298552.7:c.1208C>A	ENSP00000298552.3:p.Ser403Ter
ENST00000440111.6:c.1208C>A	ENSP00000394524.2:p.Ser403Ter
ENST00000493467.5:n.1404C>A
ENST00000545250.5:c.1055C>A	ENSP00000444017.1:p.Ser352Ter
NM_000368.4:c.1208C>A , LRG_486t1:c.1208C>A	NP_000359.1:p.Ser403Ter
NM_001162426.1:c.1205C>A	NP_001155898.1:p.Ser402Ter
NM_001162427.1:c.1055C>A	NP_001155899.1:p.Ser352Ter
XM_005272211.1:c.1208C>A	XP_005272268.1:p.Ser403Ter
XM_006717271.1:c.1208C>A	XP_006717334.1:p.Ser403Ter
XM_006717272.2:c.1208C>A	XP_006717335.1:p.Ser403Ter
XM_011518979.1:c.1208C>A	XP_011517281.1:p.Ser403Ter
NM_001362177.1:c.845C>A	NP_001349106.1:p.Ser282Ter
XM_011518979.2:c.1208C>A	XP_011517281.1:p.Ser403Ter
XM_017015096.1:c.1208C>A	XP_016870585.1:p.Ser403Ter
XM_017015097.1:c.1208C>A	XP_016870586.1:p.Ser403Ter
XM_017015098.1:c.1205C>A	XP_016870587.1:p.Ser402Ter
XM_017015100.1:c.845C>A	XP_016870589.1:p.Ser282Ter
XM_017015101.1:c.842C>A	XP_016870590.1:p.Ser281Ter
NM_000368.5:c.1208C>A MANE Select	NP_000359.1:p.Ser403Ter
NM_001162426.2:c.1205C>A	NP_001155898.1:p.Ser402Ter
NM_001162427.2:c.1055C>A	NP_001155899.1:p.Ser352Ter
NM_001362177.2:c.845C>A	NP_001349106.1:p.Ser282Ter