Canonical Allele Identifier: CA469851052

Gene: SIRT1

Linked Data

• MyVariant Identifiers: chr10:g.69647263T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887505T>A , CM000672.2:g.67887505T>A	GRCh38
NC_000010.10:g.69647263T>A , CM000672.1:g.69647263T>A	GRCh37
NC_000010.9:g.69317269T>A	NCBI36
NG_050664.1:g.7844T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.519T>A MANE Select	ENSP00000212015.6:p.Ser173=
ENST00000212015.10:c.519T>A	ENSP00000212015.6:p.Ser173=
ENST00000432464.5:c.-125T>A	ENSP00000409208.1:n.-125T>A
ENST00000473922.1:n.305T>A
ENST00000497639.5:n.308T>A
NM_001142498.1:c.-125T>A	NP_001135970.1:n.-125T>A
NM_012238.4:c.519T>A	NP_036370.2:p.Ser173=
XM_006717737.2:c.519T>A	XP_006717800.1:p.Ser173=
XM_011539561.1:c.-58T>A	XP_011537863.1:n.-58T>A
NM_012238.5:c.519T>A MANE Select	NP_036370.2:p.Ser173=
NM_001142498.2:c.-125T>A	NP_001135970.1:n.-125T>A