Canonical Allele Identifier: CA667765175

Gene: SIRT1

Linked Data

• dbSNP Id: rs1366636934
• gnomAD v3: 10-67916919-T-C
• gnomAD v4: 10-67916919-T-C
• MyVariant Identifiers: chr10:g.69676676T>C (hg19) ; chr10:g.67916919T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916919T>C , CM000672.2:g.67916919T>C	GRCh38
NC_000010.10:g.69676676T>C , CM000672.1:g.69676676T>C	GRCh37
NC_000010.9:g.69346682T>C	NCBI36
NG_050664.1:g.37258T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*326T>C MANE Select	ENSP00000212015.6:n.*326T>C
ENST00000212015.10:c.*326T>C	ENSP00000212015.6:n.*326T>C
ENST00000403579.1:c.*326T>C	ENSP00000384063.1:n.*326T>C
ENST00000406900.5:c.*326T>C	ENSP00000384508.1:n.*326T>C
ENST00000432464.5:c.*326T>C	ENSP00000409208.1:n.*326T>C
NM_001142498.1:c.*326T>C	NP_001135970.1:n.*326T>C
NM_001314049.1:c.*326T>C	NP_001300978.1:n.*326T>C
NM_012238.4:c.*326T>C	NP_036370.2:n.*326T>C
XM_006717737.2:c.*326T>C	XP_006717800.1:n.*326T>C
XM_011539561.1:c.*326T>C	XP_011537863.1:n.*326T>C
NM_012238.5:c.*326T>C MANE Select	NP_036370.2:n.*326T>C
NM_001142498.2:c.*326T>C	NP_001135970.1:n.*326T>C