Canonical Allele Identifier: CA208386880

Gene: SIRT1

Linked Data

• dbSNP Id: rs972491441
• MyVariant Identifiers: chr10:g.67917087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67917087C>T , CM000672.2:g.67917087C>T	GRCh38
NC_000010.10:g.69676844C>T , CM000672.1:g.69676844C>T	GRCh37
NC_000010.9:g.69346850C>T	NCBI36
NG_050664.1:g.37426C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*494C>T MANE Select	ENSP00000212015.6:n.*494C>T
ENST00000212015.10:c.*494C>T	ENSP00000212015.6:n.*494C>T
ENST00000403579.1:c.*494C>T	ENSP00000384063.1:n.*494C>T
ENST00000406900.5:c.*494C>T	ENSP00000384508.1:n.*494C>T
ENST00000432464.5:c.*494C>T	ENSP00000409208.1:n.*494C>T
NM_001142498.1:c.*494C>T	NP_001135970.1:n.*494C>T
NM_001314049.1:c.*494C>T	NP_001300978.1:n.*494C>T
NM_012238.4:c.*494C>T	NP_036370.2:n.*494C>T
XM_006717737.2:c.*494C>T	XP_006717800.1:n.*494C>T
XM_011539561.1:c.*494C>T	XP_011537863.1:n.*494C>T
NM_012238.5:c.*494C>T MANE Select	NP_036370.2:n.*494C>T
NM_001142498.2:c.*494C>T	NP_001135970.1:n.*494C>T