Canonical Allele Identifier: CA377038895

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67887504-C-A
• MyVariant Identifiers: chr10:g.69647262C>A (hg19) ; chr10:g.67887504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887504C>A , CM000672.2:g.67887504C>A	GRCh38
NC_000010.10:g.69647262C>A , CM000672.1:g.69647262C>A	GRCh37
NC_000010.9:g.69317268C>A	NCBI36
NG_050664.1:g.7843C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.518C>A MANE Select	ENSP00000212015.6:p.Ser173Tyr
ENST00000212015.10:c.518C>A	ENSP00000212015.6:p.Ser173Tyr
ENST00000432464.5:c.-126C>A	ENSP00000409208.1:n.-126C>A
ENST00000473922.1:n.304C>A
ENST00000497639.5:n.307C>A
NM_001142498.1:c.-126C>A	NP_001135970.1:n.-126C>A
NM_012238.4:c.518C>A	NP_036370.2:p.Ser173Tyr
XM_006717737.2:c.518C>A	XP_006717800.1:p.Ser173Tyr
XM_011539561.1:c.-59C>A	XP_011537863.1:n.-59C>A
NM_012238.5:c.518C>A MANE Select	NP_036370.2:p.Ser173Tyr
NM_001142498.2:c.-126C>A	NP_001135970.1:n.-126C>A