Canonical Allele Identifier: CA2609361526

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67908260-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67908260A>G , CM000672.2:g.67908260A>G	GRCh38
NC_000010.10:g.69668017A>G , CM000672.1:g.69668017A>G	GRCh37
NC_000010.9:g.69338023A>G	NCBI36
NG_050664.1:g.28599A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.1170+135A>G MANE Select	ENSP00000212015.6:n.1170+135A>G
ENST00000212015.10:c.1170+135A>G	ENSP00000212015.6:n.1170+135A>G
ENST00000403579.1:c.261+135A>G	ENSP00000384063.1:n.261+135A>G
ENST00000406900.5:c.261+135A>G	ENSP00000384508.1:n.261+135A>G
ENST00000432464.5:c.285+135A>G	ENSP00000409208.1:n.285+135A>G
NM_001142498.1:c.285+135A>G	NP_001135970.1:n.285+135A>G
NM_001314049.1:c.261+135A>G	NP_001300978.1:n.261+135A>G
NM_012238.4:c.1170+135A>G	NP_036370.2:n.1170+135A>G
XM_006717737.2:c.1017+135A>G	XP_006717800.1:n.1017+135A>G
XM_011539561.1:c.594+135A>G	XP_011537863.1:n.594+135A>G
NM_012238.5:c.1170+135A>G MANE Select	NP_036370.2:n.1170+135A>G
NM_001142498.2:c.285+135A>G	NP_001135970.1:n.285+135A>G