Canonical Allele Identifier: CA667765307

Gene: SIRT1

Linked Data

• dbSNP Id: rs1299638094
• gnomAD v3: 10-67917119-CTG-C
• gnomAD v4: 10-67917119-CTG-C
• MyVariant Identifiers: chr10:g.69676877_69676878del (hg19) ; chr10:g.67917120_67917121del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67917122_67917123del , CM000672.2:g.67917122_67917123del	GRCh38
NC_000010.10:g.69676879_69676880del , CM000672.1:g.69676879_69676880del	GRCh37
NC_000010.9:g.69346885_69346886del	NCBI36
NG_050664.1:g.37461_37462del

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*529_*530del MANE Select	ENSP00000212015.6:n.*529_*530del
ENST00000212015.10:c.*529_*530del	ENSP00000212015.6:n.*529_*530del
ENST00000403579.1:c.*529_*530del	ENSP00000384063.1:n.*529_*530del
ENST00000406900.5:c.*529_*530del	ENSP00000384508.1:n.*529_*530del
ENST00000432464.5:c.*529_*530del	ENSP00000409208.1:n.*529_*530del
NM_001142498.1:c.*529_*530del	NP_001135970.1:n.*529_*530del
NM_001314049.1:c.*529_*530del	NP_001300978.1:n.*529_*530del
NM_012238.4:c.*529_*530del	NP_036370.2:n.*529_*530del
XM_006717737.2:c.*529_*530del	XP_006717800.1:n.*529_*530del
XM_011539561.1:c.*529_*530del	XP_011537863.1:n.*529_*530del
NM_012238.5:c.*529_*530del MANE Select	NP_036370.2:n.*529_*530del
NM_001142498.2:c.*529_*530del	NP_001135970.1:n.*529_*530del