Canonical Allele Identifier: CA377038921

Gene: SIRT1

Linked Data

• MyVariant Identifiers: chr10:g.69647268A>C (hg19) ; chr10:g.67887510A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67887510A>C , CM000672.2:g.67887510A>C	GRCh38
NC_000010.10:g.69647268A>C , CM000672.1:g.69647268A>C	GRCh37
NC_000010.9:g.69317274A>C	NCBI36
NG_050664.1:g.7849A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.524A>C MANE Select	ENSP00000212015.6:p.Asp175Ala
ENST00000212015.10:c.524A>C	ENSP00000212015.6:p.Asp175Ala
ENST00000432464.5:c.-120A>C	ENSP00000409208.1:n.-120A>C
ENST00000473922.1:n.310A>C
ENST00000497639.5:n.313A>C
NM_001142498.1:c.-120A>C	NP_001135970.1:n.-120A>C
NM_012238.4:c.524A>C	NP_036370.2:p.Asp175Ala
XM_006717737.2:c.524A>C	XP_006717800.1:p.Asp175Ala
XM_011539561.1:c.-53A>C	XP_011537863.1:n.-53A>C
NM_012238.5:c.524A>C MANE Select	NP_036370.2:p.Asp175Ala
NM_001142498.2:c.-120A>C	NP_001135970.1:n.-120A>C