Canonical Allele Identifier: CA2609362390
Gene: SIRT1 HGNC NCBI

Linked Data

gnomAD v4: 10-67917112-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67917112T>A , CM000672.2:g.67917112T>A GRCh38
NC_000010.10:g.69676869T>A , CM000672.1:g.69676869T>A GRCh37
NC_000010.9:g.69346875T>A NCBI36
NG_050664.1:g.37451T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000212015.11:c.*519T>A MANE Select ENSP00000212015.6:n.*519T>A
ENST00000212015.10:c.*519T>A ENSP00000212015.6:n.*519T>A
ENST00000403579.1:c.*519T>A ENSP00000384063.1:n.*519T>A
ENST00000406900.5:c.*519T>A ENSP00000384508.1:n.*519T>A
ENST00000432464.5:c.*519T>A ENSP00000409208.1:n.*519T>A
NM_001142498.1:c.*519T>A NP_001135970.1:n.*519T>A
NM_001314049.1:c.*519T>A NP_001300978.1:n.*519T>A
NM_012238.4:c.*519T>A NP_036370.2:n.*519T>A
XM_006717737.2:c.*519T>A XP_006717800.1:n.*519T>A
XM_011539561.1:c.*519T>A XP_011537863.1:n.*519T>A
NM_012238.5:c.*519T>A MANE Select NP_036370.2:n.*519T>A
NM_001142498.2:c.*519T>A NP_001135970.1:n.*519T>A
Search 100 bp 5'
Search 100 bp 3'