Canonical Allele Identifier: CA377038913

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67887508-T-G
• MyVariant Identifiers: chr10:g.69647266T>G (hg19) ; chr10:g.67887508T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887508T>G , CM000672.2:g.67887508T>G	GRCh38
NC_000010.10:g.69647266T>G , CM000672.1:g.69647266T>G	GRCh37
NC_000010.9:g.69317272T>G	NCBI36
NG_050664.1:g.7847T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.522T>G MANE Select	ENSP00000212015.6:p.Ser174Arg
ENST00000212015.10:c.522T>G	ENSP00000212015.6:p.Ser174Arg
ENST00000432464.5:c.-122T>G	ENSP00000409208.1:n.-122T>G
ENST00000473922.1:n.308T>G
ENST00000497639.5:n.311T>G
NM_001142498.1:c.-122T>G	NP_001135970.1:n.-122T>G
NM_012238.4:c.522T>G	NP_036370.2:p.Ser174Arg
XM_006717737.2:c.522T>G	XP_006717800.1:p.Ser174Arg
XM_011539561.1:c.-55T>G	XP_011537863.1:n.-55T>G
NM_012238.5:c.522T>G MANE Select	NP_036370.2:p.Ser174Arg
NM_001142498.2:c.-122T>G	NP_001135970.1:n.-122T>G