Canonical Allele Identifier: CA1917084401

Gene: SIRT1

Linked Data

• dbSNP Id: rs7896005
• gnomAD v3: 10-67891367-A-T
• gnomAD v4: 10-67891367-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67891367A>T , CM000672.2:g.67891367A>T	GRCh38
NC_000010.10:g.69651125A>T , CM000672.1:g.69651125A>T	GRCh37
NC_000010.9:g.69321131A>T	NCBI36
NG_050664.1:g.11706A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.790-35A>T MANE Select	ENSP00000212015.6:n.790-35A>T
ENST00000212015.10:c.790-35A>T	ENSP00000212015.6:n.790-35A>T
ENST00000432464.5:c.-96-35A>T	ENSP00000409208.1:n.-96-35A>T
ENST00000473922.1:n.334-35A>T
ENST00000497639.5:n.579-35A>T
NM_001142498.1:c.-96-35A>T	NP_001135970.1:n.-96-35A>T
NM_012238.4:c.790-35A>T	NP_036370.2:n.790-35A>T
XM_006717737.2:c.789+2244A>T	XP_006717800.1:n.789+2244A>T
XM_011539561.1:c.214-35A>T	XP_011537863.1:n.214-35A>T
NM_012238.5:c.790-35A>T MANE Select	NP_036370.2:n.790-35A>T
NM_001142498.2:c.-96-35A>T	NP_001135970.1:n.-96-35A>T