Canonical Allele Identifier: CA377038903

Gene: SIRT1

Linked Data

• MyVariant Identifiers: chr10:g.69647264A>T (hg19) ; chr10:g.67887506A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887506A>T , CM000672.2:g.67887506A>T	GRCh38
NC_000010.10:g.69647264A>T , CM000672.1:g.69647264A>T	GRCh37
NC_000010.9:g.69317270A>T	NCBI36
NG_050664.1:g.7845A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.520A>T MANE Select	ENSP00000212015.6:p.Ser174Cys
ENST00000212015.10:c.520A>T	ENSP00000212015.6:p.Ser174Cys
ENST00000432464.5:c.-124A>T	ENSP00000409208.1:n.-124A>T
ENST00000473922.1:n.306A>T
ENST00000497639.5:n.309A>T
NM_001142498.1:c.-124A>T	NP_001135970.1:n.-124A>T
NM_012238.4:c.520A>T	NP_036370.2:p.Ser174Cys
XM_006717737.2:c.520A>T	XP_006717800.1:p.Ser174Cys
XM_011539561.1:c.-57A>T	XP_011537863.1:n.-57A>T
NM_012238.5:c.520A>T MANE Select	NP_036370.2:p.Ser174Cys
NM_001142498.2:c.-124A>T	NP_001135970.1:n.-124A>T