Canonical Allele Identifier: CA667765213

Gene: SIRT1

Linked Data

• dbSNP Id: rs1236815586
• gnomAD v3: 10-67916979-A-C
• gnomAD v4: 10-67916979-A-C
• MyVariant Identifiers: chr10:g.69676736A>C (hg19) ; chr10:g.67916979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916979A>C , CM000672.2:g.67916979A>C	GRCh38
NC_000010.10:g.69676736A>C , CM000672.1:g.69676736A>C	GRCh37
NC_000010.9:g.69346742A>C	NCBI36
NG_050664.1:g.37318A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*386A>C MANE Select	ENSP00000212015.6:n.*386A>C
ENST00000212015.10:c.*386A>C	ENSP00000212015.6:n.*386A>C
ENST00000403579.1:c.*386A>C	ENSP00000384063.1:n.*386A>C
ENST00000406900.5:c.*386A>C	ENSP00000384508.1:n.*386A>C
ENST00000432464.5:c.*386A>C	ENSP00000409208.1:n.*386A>C
NM_001142498.1:c.*386A>C	NP_001135970.1:n.*386A>C
NM_001314049.1:c.*386A>C	NP_001300978.1:n.*386A>C
NM_012238.4:c.*386A>C	NP_036370.2:n.*386A>C
XM_006717737.2:c.*386A>C	XP_006717800.1:n.*386A>C
XM_011539561.1:c.*386A>C	XP_011537863.1:n.*386A>C
NM_012238.5:c.*386A>C MANE Select	NP_036370.2:n.*386A>C
NM_001142498.2:c.*386A>C	NP_001135970.1:n.*386A>C