Canonical Allele Identifier: CA667765177

Gene: SIRT1

Linked Data

• dbSNP Id: rs1298574797
• gnomAD v3: 10-67916925-G-GT
• gnomAD v4: 10-67916925-G-GT
• MyVariant Identifiers: chr10:g.69676682_69676683insT (hg19) ; chr10:g.67916925_67916926insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916928dup , CM000672.2:g.67916928dup	GRCh38
NC_000010.10:g.69676685dup , CM000672.1:g.69676685dup	GRCh37
NC_000010.9:g.69346691dup	NCBI36
NG_050664.1:g.37267dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212015.11:c.*335dup MANE Select	ENSP00000212015.6:n.*335dup
ENST00000212015.10:c.*335dup	ENSP00000212015.6:n.*335dup
ENST00000403579.1:c.*335dup	ENSP00000384063.1:n.*335dup
ENST00000406900.5:c.*335dup	ENSP00000384508.1:n.*335dup
ENST00000432464.5:c.*335dup	ENSP00000409208.1:n.*335dup
NM_001142498.1:c.*335dup	NP_001135970.1:n.*335dup
NM_001314049.1:c.*335dup	NP_001300978.1:n.*335dup
NM_012238.4:c.*335dup	NP_036370.2:n.*335dup
XM_006717737.2:c.*335dup	XP_006717800.1:n.*335dup
XM_011539561.1:c.*335dup	XP_011537863.1:n.*335dup
NM_012238.5:c.*335dup MANE Select	NP_036370.2:n.*335dup
NM_001142498.2:c.*335dup	NP_001135970.1:n.*335dup