Canonical Allele Identifier: CA1917086663

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887218C= , CM000672.2:g.67887218C=	GRCh38
NC_000010.10:g.69646976C= , CM000672.1:g.69646976C=	GRCh37
NC_000010.9:g.69316982C=	NCBI36
NG_050664.1:g.7557C=

Transcript Alleles

HGVS	Amino-acid Change
NM_012238.5:c.431-199C= MANE Select	NP_036370.2:n.431-199C=
ENST00000212015.11:c.431-199C= MANE Select	ENSP00000212015.6:n.431-199C=
NM_001142498.1:c.-213-199C=	NP_001135970.1:n.-213-199C=
NM_001142498.2:c.-213-199C=	NP_001135970.1:n.-213-199C=
NM_012238.4:c.431-199C=	NP_036370.2:n.431-199C=
ENST00000212015.10:c.431-199C=	ENSP00000212015.6:n.431-199C=
ENST00000432464.5:c.-213-199C=	ENSP00000409208.1:n.-213-199C=
ENST00000473922.1:n.217-199C=
ENST00000497639.5:n.220-199C=
XM_006717737.2:c.431-199C=	XP_006717800.1:n.431-199C=
XM_011539561.1:c.-146-199C=	XP_011537863.1:n.-146-199C=