Canonical Allele Identifier: CA2609362366
Gene: SIRT1 HGNC NCBI

Linked Data

gnomAD v4: 10-67916988-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67916988C>A , CM000672.2:g.67916988C>A GRCh38
NC_000010.10:g.69676745C>A , CM000672.1:g.69676745C>A GRCh37
NC_000010.9:g.69346751C>A NCBI36
NG_050664.1:g.37327C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000212015.11:c.*395C>A MANE Select ENSP00000212015.6:n.*395C>A
ENST00000212015.10:c.*395C>A ENSP00000212015.6:n.*395C>A
ENST00000403579.1:c.*395C>A ENSP00000384063.1:n.*395C>A
ENST00000406900.5:c.*395C>A ENSP00000384508.1:n.*395C>A
ENST00000432464.5:c.*395C>A ENSP00000409208.1:n.*395C>A
NM_001142498.1:c.*395C>A NP_001135970.1:n.*395C>A
NM_001314049.1:c.*395C>A NP_001300978.1:n.*395C>A
NM_012238.4:c.*395C>A NP_036370.2:n.*395C>A
XM_006717737.2:c.*395C>A XP_006717800.1:n.*395C>A
XM_011539561.1:c.*395C>A XP_011537863.1:n.*395C>A
NM_012238.5:c.*395C>A MANE Select NP_036370.2:n.*395C>A
NM_001142498.2:c.*395C>A NP_001135970.1:n.*395C>A
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