Canonical Allele Identifier: CA1917101477
Gene: SIRT1 HGNC NCBI

Linked Data

dbSNP Id: rs2029947419

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67917102A>G , CM000672.2:g.67917102A>G GRCh38
NC_000010.10:g.69676859A>G , CM000672.1:g.69676859A>G GRCh37
NC_000010.9:g.69346865A>G NCBI36
NG_050664.1:g.37441A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000212015.11:c.*509A>G MANE Select ENSP00000212015.6:n.*509A>G
ENST00000212015.10:c.*509A>G ENSP00000212015.6:n.*509A>G
ENST00000403579.1:c.*509A>G ENSP00000384063.1:n.*509A>G
ENST00000406900.5:c.*509A>G ENSP00000384508.1:n.*509A>G
ENST00000432464.5:c.*509A>G ENSP00000409208.1:n.*509A>G
NM_001142498.1:c.*509A>G NP_001135970.1:n.*509A>G
NM_001314049.1:c.*509A>G NP_001300978.1:n.*509A>G
NM_012238.4:c.*509A>G NP_036370.2:n.*509A>G
XM_006717737.2:c.*509A>G XP_006717800.1:n.*509A>G
XM_011539561.1:c.*509A>G XP_011537863.1:n.*509A>G
NM_012238.5:c.*509A>G MANE Select NP_036370.2:n.*509A>G
NM_001142498.2:c.*509A>G NP_001135970.1:n.*509A>G