Canonical Allele Identifier: CA593899426

Gene: SIRT1

Linked Data

• dbSNP Id: rs1298466541
• gnomAD v2: 10-69676849-A-AT
• gnomAD v3: 10-67917092-A-AT
• gnomAD v4: 10-67917092-A-AT
• MyVariant Identifiers: chr10:g.69676849_69676850insT (hg19) ; chr10:g.67917092_67917093insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67917097dup , CM000672.2:g.67917097dup	GRCh38
NC_000010.10:g.69676854dup , CM000672.1:g.69676854dup	GRCh37
NC_000010.9:g.69346860dup	NCBI36
NG_050664.1:g.37436dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212015.11:c.*504dup MANE Select	ENSP00000212015.6:n.*504dup
ENST00000212015.10:c.*504dup	ENSP00000212015.6:n.*504dup
ENST00000403579.1:c.*504dup	ENSP00000384063.1:n.*504dup
ENST00000406900.5:c.*504dup	ENSP00000384508.1:n.*504dup
ENST00000432464.5:c.*504dup	ENSP00000409208.1:n.*504dup
NM_001142498.1:c.*504dup	NP_001135970.1:n.*504dup
NM_001314049.1:c.*504dup	NP_001300978.1:n.*504dup
NM_012238.4:c.*504dup	NP_036370.2:n.*504dup
XM_006717737.2:c.*504dup	XP_006717800.1:n.*504dup
XM_011539561.1:c.*504dup	XP_011537863.1:n.*504dup
NM_012238.5:c.*504dup MANE Select	NP_036370.2:n.*504dup
NM_001142498.2:c.*504dup	NP_001135970.1:n.*504dup