Canonical Allele Identifier: CA2723223193
Gene: SIRT3 HGNC NCBI

Linked Data

dbSNP Id: rs2133799712

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.219088_219095del , CM000673.2:g.219088_219095del GRCh38
NC_000011.9:g.219088_219095del , CM000673.1:g.219088_219095del GRCh37
NC_000011.8:g.209088_209095del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382743.9:c.970-52_970-45del MANE Select ENSP00000372191.4:n.970-52_970-45del
ENST00000382743.8:c.970-52_970-45del ENSP00000372191.4:n.970-52_970-45del
ENST00000524564.5:c.778-52_778-45del ENSP00000432937.1:n.778-52_778-45del
ENST00000525319.5:c.727-52_727-45del ENSP00000435464.1:n.727-52_727-45del
ENST00000529382.5:c.544-52_544-45del ENSP00000437216.1:n.544-52_544-45del
ENST00000529937.1:c.*1376-52_*1376-45del ENSP00000434747.1:n.*1376-52_*1376-45del
ENST00000532837.5:c.*683-52_*683-45del ENSP00000433899.1:n.*683-52_*683-45del
ENST00000532956.5:c.808-52_808-45del ENSP00000433077.1:n.808-52_808-45del
NM_001017524.2:c.544-52_544-45del NP_001017524.1:n.544-52_544-45del
NM_012239.5:c.970-52_970-45del NP_036371.1:n.970-52_970-45del
XM_005252835.1:c.970-52_970-45del XP_005252892.1:n.970-52_970-45del
XM_011519956.1:c.544-52_544-45del XP_011518258.1:n.544-52_544-45del
XM_011519957.1:c.544-52_544-45del XP_011518259.1:n.544-52_544-45del
XM_011519956.2:c.544-52_544-45del XP_011518258.1:n.544-52_544-45del
XM_011519957.2:c.544-52_544-45del XP_011518259.1:n.544-52_544-45del
XM_017017428.1:c.544-52_544-45del XP_016872917.1:n.544-52_544-45del
XM_017017429.1:c.544-52_544-45del XP_016872918.1:n.544-52_544-45del
XM_017017430.2:c.544-52_544-45del XP_016872919.1:n.544-52_544-45del
XM_017017431.1:c.544-52_544-45del XP_016872920.1:n.544-52_544-45del
XM_024448410.1:c.544-52_544-45del XP_024304178.1:n.544-52_544-45del
XR_001747817.1:n.1093-52_1093-45del
NM_012239.6:c.970-52_970-45del MANE Select NP_036371.1:n.970-52_970-45del
NM_001370310.1:c.970-52_970-45del NP_001357239.1:n.970-52_970-45del
NM_001370312.1:c.778-52_778-45del NP_001357241.1:n.778-52_778-45del
NM_001370314.1:c.808-52_808-45del NP_001357243.1:n.808-52_808-45del
NM_001370315.1:c.727-52_727-45del NP_001357244.1:n.727-52_727-45del
NM_001370316.1:c.298-52_298-45del NP_001357245.1:n.298-52_298-45del
NM_001370317.1:c.154-52_154-45del NP_001357246.1:n.154-52_154-45del
NM_001370318.1:c.544-52_544-45del NP_001357247.1:n.544-52_544-45del
NM_001370319.1:c.544-52_544-45del NP_001357248.1:n.544-52_544-45del
NM_001370320.1:c.544-52_544-45del NP_001357249.1:n.544-52_544-45del
NM_001370321.1:c.544-52_544-45del NP_001357250.1:n.544-52_544-45del
NM_001370322.1:c.544-52_544-45del NP_001357251.1:n.544-52_544-45del
NM_001370323.1:c.544-52_544-45del NP_001357252.1:n.544-52_544-45del
NM_001370324.1:c.544-2375_544-2368del NP_001357253.1:n.544-2375_544-2368del
NM_001370325.1:c.544-2375_544-2368del NP_001357254.1:n.544-2375_544-2368del
NR_163386.1:n.1159-52_1159-45del
NR_163387.1:n.1046-52_1046-45del
NR_163388.1:n.1094-52_1094-45del
NR_163389.1:n.1414-52_1414-45del
NR_163390.1:n.1094-52_1094-45del
NR_163391.1:n.1249_1256del
NR_163392.1:n.1503-52_1503-45del
NR_163393.1:n.1568-52_1568-45del
NR_163394.1:n.992-52_992-45del
NR_163395.1:n.1247-52_1247-45del
NR_163396.1:n.1073-52_1073-45del
NR_163397.1:n.879-52_879-45del
NR_163398.1:n.992-52_992-45del
NR_163399.1:n.1393-52_1393-45del
NR_163400.1:n.927-52_927-45del
NR_163401.1:n.1482-52_1482-45del
NR_163402.1:n.1491_1498del
NM_001017524.3:c.544-52_544-45del NP_001017524.1:n.544-52_544-45del