Canonical Allele Identifier: CA1917096221

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67906841T= , CM000672.2:g.67906841T=	GRCh38
NC_000010.10:g.69666598T= , CM000672.1:g.69666598T=	GRCh37
NC_000010.9:g.69336604T=	NCBI36
NG_050664.1:g.27180T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212015.11:c.994T= MANE Select	ENSP00000212015.6:p.Leu332=
ENST00000212015.10:c.994T=	ENSP00000212015.6:p.Leu332=
ENST00000403579.1:c.85T=	ENSP00000384063.1:p.Leu29=
ENST00000406900.5:c.85T=	ENSP00000384508.1:p.Leu29=
ENST00000432464.5:c.109T=	ENSP00000409208.1:p.Leu37=
ENST00000473922.1:n.538T=
NM_001142498.1:c.109T=	NP_001135970.1:p.Leu37=
NM_001314049.1:c.85T=	NP_001300978.1:p.Leu29=
NM_012238.4:c.994T=	NP_036370.2:p.Leu332=
XM_006717737.2:c.841T=	XP_006717800.1:p.Leu281=
XM_011539561.1:c.418T=	XP_011537863.1:p.Leu140=
NM_012238.5:c.994T= MANE Select	NP_036370.2:p.Leu332=
NM_001142498.2:c.109T=	NP_001135970.1:p.Leu37=