Canonical Allele Identifier: CA208369751

Gene: SIRT1

Linked Data

• dbSNP Id: rs370157323
• gnomAD v2: 10-69653675-C-T
• gnomAD v3: 10-67893917-C-T
• gnomAD v4: 10-67893917-C-T
• MyVariant Identifiers: chr10:g.69653675C>T (hg19) ; chr10:g.67893917C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67893917C>T , CM000672.2:g.67893917C>T	GRCh38
NC_000010.10:g.69653675C>T , CM000672.1:g.69653675C>T	GRCh37
NC_000010.9:g.69323681C>T	NCBI36
NG_050664.1:g.14256C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.942+2363C>T MANE Select	ENSP00000212015.6:n.942+2363C>T
ENST00000212015.10:c.942+2363C>T	ENSP00000212015.6:n.942+2363C>T
ENST00000406900.5:c.-93+2363C>T	ENSP00000384508.1:n.-93+2363C>T
ENST00000432464.5:c.57+2363C>T	ENSP00000409208.1:n.57+2363C>T
ENST00000473922.1:n.486+2363C>T
NM_001142498.1:c.57+2363C>T	NP_001135970.1:n.57+2363C>T
NM_001314049.1:c.-93+2363C>T	NP_001300978.1:n.-93+2363C>T
NM_012238.4:c.942+2363C>T	NP_036370.2:n.942+2363C>T
XM_006717737.2:c.789+4794C>T	XP_006717800.1:n.789+4794C>T
XM_011539561.1:c.366+2363C>T	XP_011537863.1:n.366+2363C>T
NM_012238.5:c.942+2363C>T MANE Select	NP_036370.2:n.942+2363C>T
NM_001142498.2:c.57+2363C>T	NP_001135970.1:n.57+2363C>T