Canonical Allele Identifier: CA1917087019

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887495A= , CM000672.2:g.67887495A=	GRCh38
NC_000010.10:g.69647253A= , CM000672.1:g.69647253A=	GRCh37
NC_000010.9:g.69317259A=	NCBI36
NG_050664.1:g.7834A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.509A= MANE Select	ENSP00000212015.6:p.His170=
ENST00000212015.10:c.509A=	ENSP00000212015.6:p.His170=
ENST00000432464.5:c.-135A=	ENSP00000409208.1:n.-135A=
ENST00000473922.1:n.295A=
ENST00000497639.5:n.298A=
NM_001142498.1:c.-135A=	NP_001135970.1:n.-135A=
NM_012238.4:c.509A=	NP_036370.2:p.His170=
XM_006717737.2:c.509A=	XP_006717800.1:p.His170=
XM_011539561.1:c.-68A=	XP_011537863.1:n.-68A=
NM_012238.5:c.509A= MANE Select	NP_036370.2:p.His170=
NM_001142498.2:c.-135A=	NP_001135970.1:n.-135A=