Canonical Allele Identifier: CA593894790

Gene: SIRT1

Linked Data

• dbSNP Id: rs1411473886
• gnomAD v2: 10-69653711-G-A
• gnomAD v3: 10-67893953-G-A
• gnomAD v4: 10-67893953-G-A
• MyVariant Identifiers: chr10:g.69653711G>A (hg19) ; chr10:g.67893953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67893953G>A , CM000672.2:g.67893953G>A	GRCh38
NC_000010.10:g.69653711G>A , CM000672.1:g.69653711G>A	GRCh37
NC_000010.9:g.69323717G>A	NCBI36
NG_050664.1:g.14292G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.942+2399G>A MANE Select	ENSP00000212015.6:n.942+2399G>A
ENST00000212015.10:c.942+2399G>A	ENSP00000212015.6:n.942+2399G>A
ENST00000406900.5:c.-93+2399G>A	ENSP00000384508.1:n.-93+2399G>A
ENST00000432464.5:c.57+2399G>A	ENSP00000409208.1:n.57+2399G>A
ENST00000473922.1:n.486+2399G>A
NM_001142498.1:c.57+2399G>A	NP_001135970.1:n.57+2399G>A
NM_001314049.1:c.-93+2399G>A	NP_001300978.1:n.-93+2399G>A
NM_012238.4:c.942+2399G>A	NP_036370.2:n.942+2399G>A
XM_006717737.2:c.789+4830G>A	XP_006717800.1:n.789+4830G>A
XM_011539561.1:c.366+2399G>A	XP_011537863.1:n.366+2399G>A
NM_012238.5:c.942+2399G>A MANE Select	NP_036370.2:n.942+2399G>A
NM_001142498.2:c.57+2399G>A	NP_001135970.1:n.57+2399G>A