Canonical Allele Identifier: CA934233719

Gene: SIRT3

Linked Data

• dbSNP Id: rs1856064439
• gnomAD v3: 11-219142-G-GGCT
• gnomAD v4: 11-219142-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219144_219145insTGC , CM000673.2:g.219144_219145insTGC	GRCh38
NC_000011.9:g.219144_219145insTGC , CM000673.1:g.219144_219145insTGC	GRCh37
NC_000011.8:g.209144_209145insTGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.970-102_970-101insAGC MANE Select	ENSP00000372191.4:n.970-102_970-101insAGC
ENST00000382743.8:c.970-102_970-101insAGC	ENSP00000372191.4:n.970-102_970-101insAGC
ENST00000524564.5:c.778-102_778-101insAGC	ENSP00000432937.1:n.778-102_778-101insAGC
ENST00000525319.5:c.727-102_727-101insAGC	ENSP00000435464.1:n.727-102_727-101insAGC
ENST00000529382.5:c.544-102_544-101insAGC	ENSP00000437216.1:n.544-102_544-101insAGC
ENST00000529937.1:c.*1376-102_*1376-101insAGC	ENSP00000434747.1:n.*1376-102_*1376-101insAGC
ENST00000532837.5:c.*683-102_*683-101insAGC	ENSP00000433899.1:n.*683-102_*683-101insAGC
ENST00000532956.5:c.808-102_808-101insAGC	ENSP00000433077.1:n.808-102_808-101insAGC
NM_001017524.2:c.544-102_544-101insAGC	NP_001017524.1:n.544-102_544-101insAGC
NM_012239.5:c.970-102_970-101insAGC	NP_036371.1:n.970-102_970-101insAGC
XM_005252835.1:c.970-102_970-101insAGC	XP_005252892.1:n.970-102_970-101insAGC
XM_011519956.1:c.544-102_544-101insAGC	XP_011518258.1:n.544-102_544-101insAGC
XM_011519957.1:c.544-102_544-101insAGC	XP_011518259.1:n.544-102_544-101insAGC
XM_011519956.2:c.544-102_544-101insAGC	XP_011518258.1:n.544-102_544-101insAGC
XM_011519957.2:c.544-102_544-101insAGC	XP_011518259.1:n.544-102_544-101insAGC
XM_017017428.1:c.544-102_544-101insAGC	XP_016872917.1:n.544-102_544-101insAGC
XM_017017429.1:c.544-102_544-101insAGC	XP_016872918.1:n.544-102_544-101insAGC
XM_017017430.2:c.544-102_544-101insAGC	XP_016872919.1:n.544-102_544-101insAGC
XM_017017431.1:c.544-102_544-101insAGC	XP_016872920.1:n.544-102_544-101insAGC
XM_024448410.1:c.544-102_544-101insAGC	XP_024304178.1:n.544-102_544-101insAGC
XR_001747817.1:n.1093-102_1093-101insAGC
NM_012239.6:c.970-102_970-101insAGC MANE Select	NP_036371.1:n.970-102_970-101insAGC
NM_001370310.1:c.970-102_970-101insAGC	NP_001357239.1:n.970-102_970-101insAGC
NM_001370312.1:c.778-102_778-101insAGC	NP_001357241.1:n.778-102_778-101insAGC
NM_001370314.1:c.808-102_808-101insAGC	NP_001357243.1:n.808-102_808-101insAGC
NM_001370315.1:c.727-102_727-101insAGC	NP_001357244.1:n.727-102_727-101insAGC
NM_001370316.1:c.298-102_298-101insAGC	NP_001357245.1:n.298-102_298-101insAGC
NM_001370317.1:c.154-102_154-101insAGC	NP_001357246.1:n.154-102_154-101insAGC
NM_001370318.1:c.544-102_544-101insAGC	NP_001357247.1:n.544-102_544-101insAGC
NM_001370319.1:c.544-102_544-101insAGC	NP_001357248.1:n.544-102_544-101insAGC
NM_001370320.1:c.544-102_544-101insAGC	NP_001357249.1:n.544-102_544-101insAGC
NM_001370321.1:c.544-102_544-101insAGC	NP_001357250.1:n.544-102_544-101insAGC
NM_001370322.1:c.544-102_544-101insAGC	NP_001357251.1:n.544-102_544-101insAGC
NM_001370323.1:c.544-102_544-101insAGC	NP_001357252.1:n.544-102_544-101insAGC
NM_001370324.1:c.544-2425_544-2424insAGC	NP_001357253.1:n.544-2425_544-2424insAGC
NM_001370325.1:c.544-2425_544-2424insAGC	NP_001357254.1:n.544-2425_544-2424insAGC
NR_163386.1:n.1159-102_1159-101insAGC
NR_163387.1:n.1046-102_1046-101insAGC
NR_163388.1:n.1094-102_1094-101insAGC
NR_163389.1:n.1414-102_1414-101insAGC
NR_163390.1:n.1094-102_1094-101insAGC
NR_163391.1:n.1199_1200insAGC
NR_163392.1:n.1503-102_1503-101insAGC
NR_163393.1:n.1568-102_1568-101insAGC
NR_163394.1:n.992-102_992-101insAGC
NR_163395.1:n.1247-102_1247-101insAGC
NR_163396.1:n.1073-102_1073-101insAGC
NR_163397.1:n.879-102_879-101insAGC
NR_163398.1:n.992-102_992-101insAGC
NR_163399.1:n.1393-102_1393-101insAGC
NR_163400.1:n.927-102_927-101insAGC
NR_163401.1:n.1482-102_1482-101insAGC
NR_163402.1:n.1441_1442insAGC
NM_001017524.3:c.544-102_544-101insAGC	NP_001017524.1:n.544-102_544-101insAGC