Canonical Allele Identifier: CA1917087022

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887506A= , CM000672.2:g.67887506A=	GRCh38
NC_000010.10:g.69647264A= , CM000672.1:g.69647264A=	GRCh37
NC_000010.9:g.69317270A=	NCBI36
NG_050664.1:g.7845A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.520A= MANE Select	ENSP00000212015.6:p.Ser174=
ENST00000212015.10:c.520A=	ENSP00000212015.6:p.Ser174=
ENST00000432464.5:c.-124A=	ENSP00000409208.1:n.-124A=
ENST00000473922.1:n.306A=
ENST00000497639.5:n.309A=
NM_001142498.1:c.-124A=	NP_001135970.1:n.-124A=
NM_012238.4:c.520A=	NP_036370.2:p.Ser174=
XM_006717737.2:c.520A=	XP_006717800.1:p.Ser174=
XM_011539561.1:c.-57A=	XP_011537863.1:n.-57A=
NM_012238.5:c.520A= MANE Select	NP_036370.2:p.Ser174=
NM_001142498.2:c.-124A=	NP_001135970.1:n.-124A=