Canonical Allele Identifier: CA593899348

Gene: SIRT1

Linked Data

• dbSNP Id: rs1383070748
• gnomAD v2: 10-69676742-C-T
• gnomAD v3: 10-67916985-C-T
• gnomAD v4: 10-67916985-C-T
• MyVariant Identifiers: chr10:g.69676742C>T (hg19) ; chr10:g.67916985C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916985C>T , CM000672.2:g.67916985C>T	GRCh38
NC_000010.10:g.69676742C>T , CM000672.1:g.69676742C>T	GRCh37
NC_000010.9:g.69346748C>T	NCBI36
NG_050664.1:g.37324C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*392C>T MANE Select	ENSP00000212015.6:n.*392C>T
ENST00000212015.10:c.*392C>T	ENSP00000212015.6:n.*392C>T
ENST00000403579.1:c.*392C>T	ENSP00000384063.1:n.*392C>T
ENST00000406900.5:c.*392C>T	ENSP00000384508.1:n.*392C>T
ENST00000432464.5:c.*392C>T	ENSP00000409208.1:n.*392C>T
NM_001142498.1:c.*392C>T	NP_001135970.1:n.*392C>T
NM_001314049.1:c.*392C>T	NP_001300978.1:n.*392C>T
NM_012238.4:c.*392C>T	NP_036370.2:n.*392C>T
XM_006717737.2:c.*392C>T	XP_006717800.1:n.*392C>T
XM_011539561.1:c.*392C>T	XP_011537863.1:n.*392C>T
NM_012238.5:c.*392C>T MANE Select	NP_036370.2:n.*392C>T
NM_001142498.2:c.*392C>T	NP_001135970.1:n.*392C>T