Canonical Allele Identifier: CA469851044

Gene: SIRT1

Linked Data

• gnomAD v4: 10-67887499-A-G
• MyVariant Identifiers: chr10:g.69647257A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887499A>G , CM000672.2:g.67887499A>G	GRCh38
NC_000010.10:g.69647257A>G , CM000672.1:g.69647257A>G	GRCh37
NC_000010.9:g.69317263A>G	NCBI36
NG_050664.1:g.7838A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.513A>G MANE Select	ENSP00000212015.6:p.Ala171=
ENST00000212015.10:c.513A>G	ENSP00000212015.6:p.Ala171=
ENST00000432464.5:c.-131A>G	ENSP00000409208.1:n.-131A>G
ENST00000473922.1:n.299A>G
ENST00000497639.5:n.302A>G
NM_001142498.1:c.-131A>G	NP_001135970.1:n.-131A>G
NM_012238.4:c.513A>G	NP_036370.2:p.Ala171=
XM_006717737.2:c.513A>G	XP_006717800.1:p.Ala171=
XM_011539561.1:c.-64A>G	XP_011537863.1:n.-64A>G
NM_012238.5:c.513A>G MANE Select	NP_036370.2:p.Ala171=
NM_001142498.2:c.-131A>G	NP_001135970.1:n.-131A>G