Canonical Allele Identifier: CA667765221

Gene: SIRT1

Linked Data

• dbSNP Id: rs1198587630
• gnomAD v3: 10-67916979-AG-A
• gnomAD v4: 10-67916979-AG-A
• MyVariant Identifiers: chr10:g.69676737del (hg19) ; chr10:g.67916980del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67916982del , CM000672.2:g.67916982del	GRCh38
NC_000010.10:g.69676739del , CM000672.1:g.69676739del	GRCh37
NC_000010.9:g.69346745del	NCBI36
NG_050664.1:g.37321del

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.*389del MANE Select	ENSP00000212015.6:n.*389del
ENST00000212015.10:c.*389del	ENSP00000212015.6:n.*389del
ENST00000403579.1:c.*389del	ENSP00000384063.1:n.*389del
ENST00000406900.5:c.*389del	ENSP00000384508.1:n.*389del
ENST00000432464.5:c.*389del	ENSP00000409208.1:n.*389del
NM_001142498.1:c.*389del	NP_001135970.1:n.*389del
NM_001314049.1:c.*389del	NP_001300978.1:n.*389del
NM_012238.4:c.*389del	NP_036370.2:n.*389del
XM_006717737.2:c.*389del	XP_006717800.1:n.*389del
XM_011539561.1:c.*389del	XP_011537863.1:n.*389del
NM_012238.5:c.*389del MANE Select	NP_036370.2:n.*389del
NM_001142498.2:c.*389del	NP_001135970.1:n.*389del