Canonical Allele Identifier: CA208386834

Gene: SIRT1

Linked Data

• dbSNP Id: rs773118531
• gnomAD v4: 10-67916970-TTAATG-T
• MyVariant Identifiers: chr10:g.69676728_69676732del (hg19) ; chr10:g.67916971_67916975del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916974_67916978del , CM000672.2:g.67916974_67916978del	GRCh38
NC_000010.10:g.69676731_69676735del , CM000672.1:g.69676731_69676735del	GRCh37
NC_000010.9:g.69346737_69346741del	NCBI36
NG_050664.1:g.37313_37317del

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*381_*385del MANE Select	ENSP00000212015.6:n.*381_*385del
ENST00000212015.10:c.*381_*385del	ENSP00000212015.6:n.*381_*385del
ENST00000403579.1:c.*381_*385del	ENSP00000384063.1:n.*381_*385del
ENST00000406900.5:c.*381_*385del	ENSP00000384508.1:n.*381_*385del
ENST00000432464.5:c.*381_*385del	ENSP00000409208.1:n.*381_*385del
NM_001142498.1:c.*381_*385del	NP_001135970.1:n.*381_*385del
NM_001314049.1:c.*381_*385del	NP_001300978.1:n.*381_*385del
NM_012238.4:c.*381_*385del	NP_036370.2:n.*381_*385del
XM_006717737.2:c.*381_*385del	XP_006717800.1:n.*381_*385del
XM_011539561.1:c.*381_*385del	XP_011537863.1:n.*381_*385del
NM_012238.5:c.*381_*385del MANE Select	NP_036370.2:n.*381_*385del
NM_001142498.2:c.*381_*385del	NP_001135970.1:n.*381_*385del