Canonical Allele Identifier: CA1917087020

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887497G= , CM000672.2:g.67887497G=	GRCh38
NC_000010.10:g.69647255G= , CM000672.1:g.69647255G=	GRCh37
NC_000010.9:g.69317261G=	NCBI36
NG_050664.1:g.7836G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.511G= MANE Select	ENSP00000212015.6:p.Ala171=
ENST00000212015.10:c.511G=	ENSP00000212015.6:p.Ala171=
ENST00000432464.5:c.-133G=	ENSP00000409208.1:n.-133G=
ENST00000473922.1:n.297G=
ENST00000497639.5:n.300G=
NM_001142498.1:c.-133G=	NP_001135970.1:n.-133G=
NM_012238.4:c.511G=	NP_036370.2:p.Ala171=
XM_006717737.2:c.511G=	XP_006717800.1:p.Ala171=
XM_011539561.1:c.-66G=	XP_011537863.1:n.-66G=
NM_012238.5:c.511G= MANE Select	NP_036370.2:p.Ala171=
NM_001142498.2:c.-133G=	NP_001135970.1:n.-133G=