Canonical Allele Identifier: CA1917087021

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887502C= , CM000672.2:g.67887502C=	GRCh38
NC_000010.10:g.69647260C= , CM000672.1:g.69647260C=	GRCh37
NC_000010.9:g.69317266C=	NCBI36
NG_050664.1:g.7841C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.516C= MANE Select	ENSP00000212015.6:p.Ser172=
ENST00000212015.10:c.516C=	ENSP00000212015.6:p.Ser172=
ENST00000432464.5:c.-128C=	ENSP00000409208.1:n.-128C=
ENST00000473922.1:n.302C=
ENST00000497639.5:n.305C=
NM_001142498.1:c.-128C=	NP_001135970.1:n.-128C=
NM_012238.4:c.516C=	NP_036370.2:p.Ser172=
XM_006717737.2:c.516C=	XP_006717800.1:p.Ser172=
XM_011539561.1:c.-61C=	XP_011537863.1:n.-61C=
NM_012238.5:c.516C= MANE Select	NP_036370.2:p.Ser172=
NM_001142498.2:c.-128C=	NP_001135970.1:n.-128C=