Canonical Allele Identifier: CA674601754

Gene: SIRT3

Linked Data

• dbSNP Id: rs1195706226
• gnomAD v3: 11-219396-ACG-A
• gnomAD v4: 11-219396-ACG-A
• MyVariant Identifiers: chr11:g.219397_219398del (hg19) ; chr11:g.219397_219398del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219398_219399del , CM000673.2:g.219398_219399del	GRCh38
NC_000011.9:g.219398_219399del , CM000673.1:g.219398_219399del	GRCh37
NC_000011.8:g.209398_209399del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.970-357_970-356del MANE Select	ENSP00000372191.4:n.970-357_970-356del
ENST00000382743.8:c.970-357_970-356del	ENSP00000372191.4:n.970-357_970-356del
ENST00000524564.5:c.778-357_778-356del	ENSP00000432937.1:n.778-357_778-356del
ENST00000525319.5:c.727-357_727-356del	ENSP00000435464.1:n.727-357_727-356del
ENST00000529382.5:c.544-357_544-356del	ENSP00000437216.1:n.544-357_544-356del
ENST00000529937.1:c.*1376-357_*1376-356del	ENSP00000434747.1:n.*1376-357_*1376-356del
ENST00000532837.5:c.*683-357_*683-356del	ENSP00000433899.1:n.*683-357_*683-356del
ENST00000532956.5:c.808-357_808-356del	ENSP00000433077.1:n.808-357_808-356del
NM_001017524.2:c.544-357_544-356del	NP_001017524.1:n.544-357_544-356del
NM_012239.5:c.970-357_970-356del	NP_036371.1:n.970-357_970-356del
XM_005252835.1:c.970-357_970-356del	XP_005252892.1:n.970-357_970-356del
XM_011519956.1:c.544-357_544-356del	XP_011518258.1:n.544-357_544-356del
XM_011519957.1:c.544-357_544-356del	XP_011518259.1:n.544-357_544-356del
XM_011519956.2:c.544-357_544-356del	XP_011518258.1:n.544-357_544-356del
XM_011519957.2:c.544-357_544-356del	XP_011518259.1:n.544-357_544-356del
XM_017017428.1:c.544-357_544-356del	XP_016872917.1:n.544-357_544-356del
XM_017017429.1:c.544-357_544-356del	XP_016872918.1:n.544-357_544-356del
XM_017017430.2:c.544-357_544-356del	XP_016872919.1:n.544-357_544-356del
XM_017017431.1:c.544-357_544-356del	XP_016872920.1:n.544-357_544-356del
XM_024448410.1:c.544-357_544-356del	XP_024304178.1:n.544-357_544-356del
XR_001747817.1:n.1093-357_1093-356del
NM_012239.6:c.970-357_970-356del MANE Select	NP_036371.1:n.970-357_970-356del
NM_001370310.1:c.970-357_970-356del	NP_001357239.1:n.970-357_970-356del
NM_001370312.1:c.778-357_778-356del	NP_001357241.1:n.778-357_778-356del
NM_001370314.1:c.808-357_808-356del	NP_001357243.1:n.808-357_808-356del
NM_001370315.1:c.727-357_727-356del	NP_001357244.1:n.727-357_727-356del
NM_001370316.1:c.298-357_298-356del	NP_001357245.1:n.298-357_298-356del
NM_001370317.1:c.154-357_154-356del	NP_001357246.1:n.154-357_154-356del
NM_001370318.1:c.544-357_544-356del	NP_001357247.1:n.544-357_544-356del
NM_001370319.1:c.544-357_544-356del	NP_001357248.1:n.544-357_544-356del
NM_001370320.1:c.544-357_544-356del	NP_001357249.1:n.544-357_544-356del
NM_001370321.1:c.544-357_544-356del	NP_001357250.1:n.544-357_544-356del
NM_001370322.1:c.544-357_544-356del	NP_001357251.1:n.544-357_544-356del
NM_001370323.1:c.544-357_544-356del	NP_001357252.1:n.544-357_544-356del
NM_001370324.1:c.544-2680_544-2679del	NP_001357253.1:n.544-2680_544-2679del
NM_001370325.1:c.544-2680_544-2679del	NP_001357254.1:n.544-2680_544-2679del
NR_163386.1:n.1159-357_1159-356del
NR_163387.1:n.1046-357_1046-356del
NR_163388.1:n.1094-357_1094-356del
NR_163389.1:n.1414-357_1414-356del
NR_163390.1:n.1094-357_1094-356del
NR_163391.1:n.944_945del
NR_163392.1:n.1503-357_1503-356del
NR_163393.1:n.1568-357_1568-356del
NR_163394.1:n.992-357_992-356del
NR_163395.1:n.1247-357_1247-356del
NR_163396.1:n.1073-357_1073-356del
NR_163397.1:n.879-357_879-356del
NR_163398.1:n.992-357_992-356del
NR_163399.1:n.1393-357_1393-356del
NR_163400.1:n.927-357_927-356del
NR_163401.1:n.1482-357_1482-356del
NR_163402.1:n.1186_1187del
NM_001017524.3:c.544-357_544-356del	NP_001017524.1:n.544-357_544-356del