Canonical Allele Identifier: CA378857885

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.219032A>C (hg19) ; chr11:g.219032A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219032A>C , CM000673.2:g.219032A>C	GRCh38
NC_000011.9:g.219032A>C , CM000673.1:g.219032A>C	GRCh37
NC_000011.8:g.209032A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.979T>G MANE Select	ENSP00000372191.4:p.Phe327Val
ENST00000382743.8:c.979T>G	ENSP00000372191.4:p.Phe327Val
ENST00000524564.5:c.787T>G	ENSP00000432937.1:p.Phe263Val
ENST00000525319.5:c.736T>G	ENSP00000435464.1:p.Phe246Val
ENST00000529382.5:c.553T>G	ENSP00000437216.1:p.Phe185Val
ENST00000529937.1:c.*1385T>G	ENSP00000434747.1:n.*1385T>G
ENST00000532837.5:c.*692T>G	ENSP00000433899.1:n.*692T>G
ENST00000532956.5:c.817T>G	ENSP00000433077.1:p.Phe273Val
NM_001017524.2:c.553T>G	NP_001017524.1:p.Phe185Val
NM_012239.5:c.979T>G	NP_036371.1:p.Phe327Val
XM_005252835.1:c.979T>G	XP_005252892.1:p.Phe327Val
XM_011519956.1:c.553T>G	XP_011518258.1:p.Phe185Val
XM_011519957.1:c.553T>G	XP_011518259.1:p.Phe185Val
XM_011519956.2:c.553T>G	XP_011518258.1:p.Phe185Val
XM_011519957.2:c.553T>G	XP_011518259.1:p.Phe185Val
XM_017017428.1:c.553T>G	XP_016872917.1:p.Phe185Val
XM_017017429.1:c.553T>G	XP_016872918.1:p.Phe185Val
XM_017017430.2:c.553T>G	XP_016872919.1:p.Phe185Val
XM_017017431.1:c.553T>G	XP_016872920.1:p.Phe185Val
XM_024448410.1:c.553T>G	XP_024304178.1:p.Phe185Val
XR_001747817.1:n.1102T>G
NM_012239.6:c.979T>G MANE Select	NP_036371.1:p.Phe327Val
NM_001370310.1:c.979T>G	NP_001357239.1:p.Phe327Val
NM_001370312.1:c.787T>G	NP_001357241.1:p.Phe263Val
NM_001370314.1:c.817T>G	NP_001357243.1:p.Phe273Val
NM_001370315.1:c.736T>G	NP_001357244.1:p.Phe246Val
NM_001370316.1:c.307T>G	NP_001357245.1:p.Phe103Val
NM_001370317.1:c.163T>G	NP_001357246.1:p.Phe55Val
NM_001370318.1:c.553T>G	NP_001357247.1:p.Phe185Val
NM_001370319.1:c.553T>G	NP_001357248.1:p.Phe185Val
NM_001370320.1:c.553T>G	NP_001357249.1:p.Phe185Val
NM_001370321.1:c.553T>G	NP_001357250.1:p.Phe185Val
NM_001370322.1:c.553T>G	NP_001357251.1:p.Phe185Val
NM_001370323.1:c.553T>G	NP_001357252.1:p.Phe185Val
NM_001370324.1:c.544-2314T>G	NP_001357253.1:n.544-2314T>G
NM_001370325.1:c.544-2314T>G	NP_001357254.1:n.544-2314T>G
NR_163386.1:n.1168T>G
NR_163387.1:n.1055T>G
NR_163388.1:n.1103T>G
NR_163389.1:n.1423T>G
NR_163390.1:n.1103T>G
NR_163391.1:n.1310T>G
NR_163392.1:n.1512T>G
NR_163393.1:n.1577T>G
NR_163394.1:n.1001T>G
NR_163395.1:n.1256T>G
NR_163396.1:n.1082T>G
NR_163397.1:n.888T>G
NR_163398.1:n.1001T>G
NR_163399.1:n.1402T>G
NR_163400.1:n.936T>G
NR_163401.1:n.1491T>G
NR_163402.1:n.1552T>G
NM_001017524.3:c.553T>G	NP_001017524.1:p.Phe185Val