Canonical Allele Identifier: CA2611651067

Gene: SIRT3

Linked Data

• gnomAD v4: 11-219067-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219070_219071del , CM000673.2:g.219070_219071del	GRCh38
NC_000011.9:g.219070_219071del , CM000673.1:g.219070_219071del	GRCh37
NC_000011.8:g.209070_209071del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.970-28_970-27del MANE Select	ENSP00000372191.4:n.970-28_970-27del
ENST00000382743.8:c.970-28_970-27del	ENSP00000372191.4:n.970-28_970-27del
ENST00000524564.5:c.778-28_778-27del	ENSP00000432937.1:n.778-28_778-27del
ENST00000525319.5:c.727-28_727-27del	ENSP00000435464.1:n.727-28_727-27del
ENST00000529382.5:c.544-28_544-27del	ENSP00000437216.1:n.544-28_544-27del
ENST00000529937.1:c.*1376-28_*1376-27del	ENSP00000434747.1:n.*1376-28_*1376-27del
ENST00000532837.5:c.*683-28_*683-27del	ENSP00000433899.1:n.*683-28_*683-27del
ENST00000532956.5:c.808-28_808-27del	ENSP00000433077.1:n.808-28_808-27del
NM_001017524.2:c.544-28_544-27del	NP_001017524.1:n.544-28_544-27del
NM_012239.5:c.970-28_970-27del	NP_036371.1:n.970-28_970-27del
XM_005252835.1:c.970-28_970-27del	XP_005252892.1:n.970-28_970-27del
XM_011519956.1:c.544-28_544-27del	XP_011518258.1:n.544-28_544-27del
XM_011519957.1:c.544-28_544-27del	XP_011518259.1:n.544-28_544-27del
XM_011519956.2:c.544-28_544-27del	XP_011518258.1:n.544-28_544-27del
XM_011519957.2:c.544-28_544-27del	XP_011518259.1:n.544-28_544-27del
XM_017017428.1:c.544-28_544-27del	XP_016872917.1:n.544-28_544-27del
XM_017017429.1:c.544-28_544-27del	XP_016872918.1:n.544-28_544-27del
XM_017017430.2:c.544-28_544-27del	XP_016872919.1:n.544-28_544-27del
XM_017017431.1:c.544-28_544-27del	XP_016872920.1:n.544-28_544-27del
XM_024448410.1:c.544-28_544-27del	XP_024304178.1:n.544-28_544-27del
XR_001747817.1:n.1093-28_1093-27del
NM_012239.6:c.970-28_970-27del MANE Select	NP_036371.1:n.970-28_970-27del
NM_001370310.1:c.970-28_970-27del	NP_001357239.1:n.970-28_970-27del
NM_001370312.1:c.778-28_778-27del	NP_001357241.1:n.778-28_778-27del
NM_001370314.1:c.808-28_808-27del	NP_001357243.1:n.808-28_808-27del
NM_001370315.1:c.727-28_727-27del	NP_001357244.1:n.727-28_727-27del
NM_001370316.1:c.298-28_298-27del	NP_001357245.1:n.298-28_298-27del
NM_001370317.1:c.154-28_154-27del	NP_001357246.1:n.154-28_154-27del
NM_001370318.1:c.544-28_544-27del	NP_001357247.1:n.544-28_544-27del
NM_001370319.1:c.544-28_544-27del	NP_001357248.1:n.544-28_544-27del
NM_001370320.1:c.544-28_544-27del	NP_001357249.1:n.544-28_544-27del
NM_001370321.1:c.544-28_544-27del	NP_001357250.1:n.544-28_544-27del
NM_001370322.1:c.544-28_544-27del	NP_001357251.1:n.544-28_544-27del
NM_001370323.1:c.544-28_544-27del	NP_001357252.1:n.544-28_544-27del
NM_001370324.1:c.544-2351_544-2350del	NP_001357253.1:n.544-2351_544-2350del
NM_001370325.1:c.544-2351_544-2350del	NP_001357254.1:n.544-2351_544-2350del
NR_163386.1:n.1159-28_1159-27del
NR_163387.1:n.1046-28_1046-27del
NR_163388.1:n.1094-28_1094-27del
NR_163389.1:n.1414-28_1414-27del
NR_163390.1:n.1094-28_1094-27del
NR_163391.1:n.1273_1274del
NR_163392.1:n.1503-28_1503-27del
NR_163393.1:n.1568-28_1568-27del
NR_163394.1:n.992-28_992-27del
NR_163395.1:n.1247-28_1247-27del
NR_163396.1:n.1073-28_1073-27del
NR_163397.1:n.879-28_879-27del
NR_163398.1:n.992-28_992-27del
NR_163399.1:n.1393-28_1393-27del
NR_163400.1:n.927-28_927-27del
NR_163401.1:n.1482-28_1482-27del
NR_163402.1:n.1515_1516del
NM_001017524.3:c.544-28_544-27del	NP_001017524.1:n.544-28_544-27del