Canonical Allele Identifier: CA16612586

Gene: TSC1

Linked Data

• ClinVar Variation Id: 416686
• ClinVar RCV Id: RCV000473192 ; RCV002350040 ; RCV003328589 ; RCV004002203
• dbSNP Id: rs1060504861
• gnomAD v4: 9-132910640-G-C
• MyVariant Identifiers: chr9:g.135786027G>C (hg19) ; chr9:g.132910640G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132910640G>C , CM000671.2:g.132910640G>C	GRCh38
NC_000009.11:g.135786027G>C , CM000671.1:g.135786027G>C	GRCh37
NC_000009.10:g.134775848G>C	NCBI36
NG_012386.1:g.38994C>G , LRG_486:g.38994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1191C>G	ENSP00000496126.2:p.Ala397=
ENST00000490179.4:c.1194C>G	ENSP00000495533.2:p.Ala398=
ENST00000642261.2:c.1194C>G	ENSP00000494743.2:p.Ala398=
ENST00000643275.2:c.1194C>G	ENSP00000495598.2:p.Ala398=
ENST00000643362.2:c.876+813C>G	ENSP00000496398.2:n.876+813C>G
ENST00000643625.2:c.1194C>G	ENSP00000495546.2:p.Ala398=
ENST00000643691.2:c.831C>G	ENSP00000494916.2:p.Ala277=
ENST00000644184.2:c.1194C>G	ENSP00000495428.2:p.Ala398=
ENST00000645129.2:c.1038C>G	ENSP00000493639.2:p.Ala346=
ENST00000646440.2:c.1194C>G	ENSP00000495830.2:p.Ala398=
ENST00000647078.2:c.*88C>G	ENSP00000496066.1:n.*88C>G
ENST00000298552.9:c.1194C>G MANE Select	ENSP00000298552.3:p.Ala398=
ENST00000493467.6:n.465C>G
ENST00000642344.1:c.*935C>G	ENSP00000494847.1:n.*935C>G
ENST00000642617.1:c.1191C>G	ENSP00000493773.1:p.Ala397=
ENST00000642627.1:c.1191C>G	ENSP00000496772.1:p.Ala397=
ENST00000642646.1:c.1194C>G	ENSP00000496292.1:p.Ala398=
ENST00000642745.1:c.1194C>G	ENSP00000493963.1:p.Ala398=
ENST00000642811.1:c.*964C>G	ENSP00000495554.1:n.*964C>G
ENST00000643072.1:c.1041C>G	ENSP00000496691.1:p.Ala347=
ENST00000643362.1:c.876+813C>G	ENSP00000496398.1:n.876+813C>G
ENST00000643583.1:c.1194C>G	ENSP00000494685.1:p.Ala398=
ENST00000643875.1:c.1194C>G	ENSP00000495158.1:p.Ala398=
ENST00000644097.1:c.1191C>G	ENSP00000494682.1:p.Ala397=
ENST00000644255.1:c.*961C>G	ENSP00000493608.1:n.*961C>G
ENST00000644319.1:n.1569C>G
ENST00000644997.1:c.*848C>G	ENSP00000495654.1:n.*848C>G
ENST00000645129.1:c.1038C>G	ENSP00000493639.1:p.Ala346=
ENST00000645150.1:c.1194C>G	ENSP00000494365.1:p.Ala398=
ENST00000645901.1:n.2045C>G
ENST00000646391.1:c.*964C>G	ENSP00000494104.1:n.*964C>G
ENST00000646625.1:c.1194C>G	ENSP00000496263.1:p.Ala398=
ENST00000647078.1:c.*88C>G	ENSP00000496066.1:n.*88C>G
ENST00000647279.1:c.*433C>G	ENSP00000494502.1:n.*433C>G
ENST00000647462.1:c.1191C>G	ENSP00000495821.1:p.Ala397=
ENST00000647506.1:n.2070C>G
ENST00000647534.1:n.258C>G
ENST00000298552.7:c.1194C>G	ENSP00000298552.3:p.Ala398=
ENST00000440111.6:c.1194C>G	ENSP00000394524.2:p.Ala398=
ENST00000493467.5:n.1390C>G
ENST00000545250.5:c.1041C>G	ENSP00000444017.1:p.Ala347=
NM_000368.4:c.1194C>G , LRG_486t1:c.1194C>G	NP_000359.1:p.Ala398=
NM_001162426.1:c.1191C>G	NP_001155898.1:p.Ala397=
NM_001162427.1:c.1041C>G	NP_001155899.1:p.Ala347=
XM_005272211.1:c.1194C>G	XP_005272268.1:p.Ala398=
XM_006717271.1:c.1194C>G	XP_006717334.1:p.Ala398=
XM_006717272.2:c.1194C>G	XP_006717335.1:p.Ala398=
XM_011518979.1:c.1194C>G	XP_011517281.1:p.Ala398=
NM_001362177.1:c.831C>G	NP_001349106.1:p.Ala277=
XM_011518979.2:c.1194C>G	XP_011517281.1:p.Ala398=
XM_017015096.1:c.1194C>G	XP_016870585.1:p.Ala398=
XM_017015097.1:c.1194C>G	XP_016870586.1:p.Ala398=
XM_017015098.1:c.1191C>G	XP_016870587.1:p.Ala397=
XM_017015100.1:c.831C>G	XP_016870589.1:p.Ala277=
XM_017015101.1:c.828C>G	XP_016870590.1:p.Ala276=
NM_000368.5:c.1194C>G MANE Select	NP_000359.1:p.Ala398=
NM_001162426.2:c.1191C>G	NP_001155898.1:p.Ala397=
NM_001162427.2:c.1041C>G	NP_001155899.1:p.Ala347=
NM_001362177.2:c.831C>G	NP_001349106.1:p.Ala277=