Canonical Allele Identifier: CA2514011550

Gene: SIRT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219252_219253insAT , CM000673.2:g.219252_219253insAT	GRCh38
NC_000011.9:g.219252_219253insAT , CM000673.1:g.219252_219253insAT	GRCh37
NC_000011.8:g.209252_209253insAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.970-212_970-211insAT MANE Select	ENSP00000372191.4:n.970-212_970-211insAT
ENST00000382743.8:c.970-212_970-211insAT	ENSP00000372191.4:n.970-212_970-211insAT
ENST00000524564.5:c.778-212_778-211insAT	ENSP00000432937.1:n.778-212_778-211insAT
ENST00000525319.5:c.727-212_727-211insAT	ENSP00000435464.1:n.727-212_727-211insAT
ENST00000529382.5:c.544-212_544-211insAT	ENSP00000437216.1:n.544-212_544-211insAT
ENST00000529937.1:c.*1376-212_*1376-211insAT	ENSP00000434747.1:n.*1376-212_*1376-211insAT
ENST00000532837.5:c.*683-212_*683-211insAT	ENSP00000433899.1:n.*683-212_*683-211insAT
ENST00000532956.5:c.808-212_808-211insAT	ENSP00000433077.1:n.808-212_808-211insAT
NM_001017524.2:c.544-212_544-211insAT	NP_001017524.1:n.544-212_544-211insAT
NM_012239.5:c.970-212_970-211insAT	NP_036371.1:n.970-212_970-211insAT
XM_005252835.1:c.970-212_970-211insAT	XP_005252892.1:n.970-212_970-211insAT
XM_011519956.1:c.544-212_544-211insAT	XP_011518258.1:n.544-212_544-211insAT
XM_011519957.1:c.544-212_544-211insAT	XP_011518259.1:n.544-212_544-211insAT
XM_011519956.2:c.544-212_544-211insAT	XP_011518258.1:n.544-212_544-211insAT
XM_011519957.2:c.544-212_544-211insAT	XP_011518259.1:n.544-212_544-211insAT
XM_017017428.1:c.544-212_544-211insAT	XP_016872917.1:n.544-212_544-211insAT
XM_017017429.1:c.544-212_544-211insAT	XP_016872918.1:n.544-212_544-211insAT
XM_017017430.2:c.544-212_544-211insAT	XP_016872919.1:n.544-212_544-211insAT
XM_017017431.1:c.544-212_544-211insAT	XP_016872920.1:n.544-212_544-211insAT
XM_024448410.1:c.544-212_544-211insAT	XP_024304178.1:n.544-212_544-211insAT
XR_001747817.1:n.1093-212_1093-211insAT
NM_012239.6:c.970-212_970-211insAT MANE Select	NP_036371.1:n.970-212_970-211insAT
NM_001370310.1:c.970-212_970-211insAT	NP_001357239.1:n.970-212_970-211insAT
NM_001370312.1:c.778-212_778-211insAT	NP_001357241.1:n.778-212_778-211insAT
NM_001370314.1:c.808-212_808-211insAT	NP_001357243.1:n.808-212_808-211insAT
NM_001370315.1:c.727-212_727-211insAT	NP_001357244.1:n.727-212_727-211insAT
NM_001370316.1:c.298-212_298-211insAT	NP_001357245.1:n.298-212_298-211insAT
NM_001370317.1:c.154-212_154-211insAT	NP_001357246.1:n.154-212_154-211insAT
NM_001370318.1:c.544-212_544-211insAT	NP_001357247.1:n.544-212_544-211insAT
NM_001370319.1:c.544-212_544-211insAT	NP_001357248.1:n.544-212_544-211insAT
NM_001370320.1:c.544-212_544-211insAT	NP_001357249.1:n.544-212_544-211insAT
NM_001370321.1:c.544-212_544-211insAT	NP_001357250.1:n.544-212_544-211insAT
NM_001370322.1:c.544-212_544-211insAT	NP_001357251.1:n.544-212_544-211insAT
NM_001370323.1:c.544-212_544-211insAT	NP_001357252.1:n.544-212_544-211insAT
NM_001370324.1:c.544-2535_544-2534insAT	NP_001357253.1:n.544-2535_544-2534insAT
NM_001370325.1:c.544-2535_544-2534insAT	NP_001357254.1:n.544-2535_544-2534insAT
NR_163386.1:n.1159-212_1159-211insAT
NR_163387.1:n.1046-212_1046-211insAT
NR_163388.1:n.1094-212_1094-211insAT
NR_163389.1:n.1414-212_1414-211insAT
NR_163390.1:n.1094-212_1094-211insAT
NR_163391.1:n.1089_1090insAT
NR_163392.1:n.1503-212_1503-211insAT
NR_163393.1:n.1568-212_1568-211insAT
NR_163394.1:n.992-212_992-211insAT
NR_163395.1:n.1247-212_1247-211insAT
NR_163396.1:n.1073-212_1073-211insAT
NR_163397.1:n.879-212_879-211insAT
NR_163398.1:n.992-212_992-211insAT
NR_163399.1:n.1393-212_1393-211insAT
NR_163400.1:n.927-212_927-211insAT
NR_163401.1:n.1482-212_1482-211insAT
NR_163402.1:n.1331_1332insAT
NM_001017524.3:c.544-212_544-211insAT	NP_001017524.1:n.544-212_544-211insAT