Canonical Allele Identifier: CA377038916

Gene: SIRT1

Linked Data

• MyVariant Identifiers: chr10:g.69647267G>A (hg19) ; chr10:g.67887509G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887509G>A , CM000672.2:g.67887509G>A	GRCh38
NC_000010.10:g.69647267G>A , CM000672.1:g.69647267G>A	GRCh37
NC_000010.9:g.69317273G>A	NCBI36
NG_050664.1:g.7848G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.523G>A MANE Select	ENSP00000212015.6:p.Asp175Asn
ENST00000212015.10:c.523G>A	ENSP00000212015.6:p.Asp175Asn
ENST00000432464.5:c.-121G>A	ENSP00000409208.1:n.-121G>A
ENST00000473922.1:n.309G>A
ENST00000497639.5:n.312G>A
NM_001142498.1:c.-121G>A	NP_001135970.1:n.-121G>A
NM_012238.4:c.523G>A	NP_036370.2:p.Asp175Asn
XM_006717737.2:c.523G>A	XP_006717800.1:p.Asp175Asn
XM_011539561.1:c.-54G>A	XP_011537863.1:n.-54G>A
NM_012238.5:c.523G>A MANE Select	NP_036370.2:p.Asp175Asn
NM_001142498.2:c.-121G>A	NP_001135970.1:n.-121G>A