Canonical Allele Identifier: CA377038892

Gene: SIRT1

Linked Data

• MyVariant Identifiers: chr10:g.69647261T>C (hg19) ; chr10:g.67887503T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887503T>C , CM000672.2:g.67887503T>C	GRCh38
NC_000010.10:g.69647261T>C , CM000672.1:g.69647261T>C	GRCh37
NC_000010.9:g.69317267T>C	NCBI36
NG_050664.1:g.7842T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.517T>C MANE Select	ENSP00000212015.6:p.Ser173Pro
ENST00000212015.10:c.517T>C	ENSP00000212015.6:p.Ser173Pro
ENST00000432464.5:c.-127T>C	ENSP00000409208.1:n.-127T>C
ENST00000473922.1:n.303T>C
ENST00000497639.5:n.306T>C
NM_001142498.1:c.-127T>C	NP_001135970.1:n.-127T>C
NM_012238.4:c.517T>C	NP_036370.2:p.Ser173Pro
XM_006717737.2:c.517T>C	XP_006717800.1:p.Ser173Pro
XM_011539561.1:c.-60T>C	XP_011537863.1:n.-60T>C
NM_012238.5:c.517T>C MANE Select	NP_036370.2:p.Ser173Pro
NM_001142498.2:c.-127T>C	NP_001135970.1:n.-127T>C