Canonical Allele Identifier: CA1917101404
Gene: SIRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67916964_67916969delinsGTTAAA , CM000672.2:g.67916964_67916969delinsGTTAAA GRCh38
NC_000010.10:g.69676721_69676726delinsGTTAAA , CM000672.1:g.69676721_69676726delinsGTTAAA GRCh37
NC_000010.9:g.69346727_69346732delinsGTTAAA NCBI36
NG_050664.1:g.37303_37308delinsGTTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000212015.11:c.*371_*376delinsGTTAAA MANE Select ENSP00000212015.6:n.*371_*376delinsGTTAAA
ENST00000212015.10:c.*371_*376delinsGTTAAA ENSP00000212015.6:n.*371_*376delinsGTTAAA
ENST00000403579.1:c.*371_*376delinsGTTAAA ENSP00000384063.1:n.*371_*376delinsGTTAAA
ENST00000406900.5:c.*371_*376delinsGTTAAA ENSP00000384508.1:n.*371_*376delinsGTTAAA
ENST00000432464.5:c.*371_*376delinsGTTAAA ENSP00000409208.1:n.*371_*376delinsGTTAAA
NM_001142498.1:c.*371_*376delinsGTTAAA NP_001135970.1:n.*371_*376delinsGTTAAA
NM_001314049.1:c.*371_*376delinsGTTAAA NP_001300978.1:n.*371_*376delinsGTTAAA
NM_012238.4:c.*371_*376delinsGTTAAA NP_036370.2:n.*371_*376delinsGTTAAA
XM_006717737.2:c.*371_*376delinsGTTAAA XP_006717800.1:n.*371_*376delinsGTTAAA
XM_011539561.1:c.*371_*376delinsGTTAAA XP_011537863.1:n.*371_*376delinsGTTAAA
NM_012238.5:c.*371_*376delinsGTTAAA MANE Select NP_036370.2:n.*371_*376delinsGTTAAA
NM_001142498.2:c.*371_*376delinsGTTAAA NP_001135970.1:n.*371_*376delinsGTTAAA