Canonical Allele Identifier: CA378857852

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.219016T>A (hg19) ; chr11:g.219016T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219016T>A , CM000673.2:g.219016T>A	GRCh38
NC_000011.9:g.219016T>A , CM000673.1:g.219016T>A	GRCh37
NC_000011.8:g.209016T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.995A>T MANE Select	ENSP00000372191.4:p.Glu332Val
ENST00000382743.8:c.995A>T	ENSP00000372191.4:p.Glu332Val
ENST00000524564.5:c.803A>T	ENSP00000432937.1:p.Glu268Val
ENST00000525319.5:c.752A>T	ENSP00000435464.1:p.Glu251Val
ENST00000529382.5:c.569A>T	ENSP00000437216.1:p.Glu190Val
ENST00000529937.1:c.*1401A>T	ENSP00000434747.1:n.*1401A>T
ENST00000532837.5:c.*708A>T	ENSP00000433899.1:n.*708A>T
ENST00000532956.5:c.833A>T	ENSP00000433077.1:p.Glu278Val
NM_001017524.2:c.569A>T	NP_001017524.1:p.Glu190Val
NM_012239.5:c.995A>T	NP_036371.1:p.Glu332Val
XM_005252835.1:c.995A>T	XP_005252892.1:p.Glu332Val
XM_011519956.1:c.569A>T	XP_011518258.1:p.Glu190Val
XM_011519957.1:c.569A>T	XP_011518259.1:p.Glu190Val
XM_011519956.2:c.569A>T	XP_011518258.1:p.Glu190Val
XM_011519957.2:c.569A>T	XP_011518259.1:p.Glu190Val
XM_017017428.1:c.569A>T	XP_016872917.1:p.Glu190Val
XM_017017429.1:c.569A>T	XP_016872918.1:p.Glu190Val
XM_017017430.2:c.569A>T	XP_016872919.1:p.Glu190Val
XM_017017431.1:c.569A>T	XP_016872920.1:p.Glu190Val
XM_024448410.1:c.569A>T	XP_024304178.1:p.Glu190Val
XR_001747817.1:n.1118A>T
NM_012239.6:c.995A>T MANE Select	NP_036371.1:p.Glu332Val
NM_001370310.1:c.995A>T	NP_001357239.1:p.Glu332Val
NM_001370312.1:c.803A>T	NP_001357241.1:p.Glu268Val
NM_001370314.1:c.833A>T	NP_001357243.1:p.Glu278Val
NM_001370315.1:c.752A>T	NP_001357244.1:p.Glu251Val
NM_001370316.1:c.323A>T	NP_001357245.1:p.Glu108Val
NM_001370317.1:c.179A>T	NP_001357246.1:p.Glu60Val
NM_001370318.1:c.569A>T	NP_001357247.1:p.Glu190Val
NM_001370319.1:c.569A>T	NP_001357248.1:p.Glu190Val
NM_001370320.1:c.569A>T	NP_001357249.1:p.Glu190Val
NM_001370321.1:c.569A>T	NP_001357250.1:p.Glu190Val
NM_001370322.1:c.569A>T	NP_001357251.1:p.Glu190Val
NM_001370323.1:c.569A>T	NP_001357252.1:p.Glu190Val
NM_001370324.1:c.544-2298A>T	NP_001357253.1:n.544-2298A>T
NM_001370325.1:c.544-2298A>T	NP_001357254.1:n.544-2298A>T
NR_163386.1:n.1184A>T
NR_163387.1:n.1071A>T
NR_163388.1:n.1119A>T
NR_163389.1:n.1439A>T
NR_163390.1:n.1119A>T
NR_163391.1:n.1326A>T
NR_163392.1:n.1528A>T
NR_163393.1:n.1593A>T
NR_163394.1:n.1017A>T
NR_163395.1:n.1272A>T
NR_163396.1:n.1098A>T
NR_163397.1:n.904A>T
NR_163398.1:n.1017A>T
NR_163399.1:n.1418A>T
NR_163400.1:n.952A>T
NR_163401.1:n.1507A>T
NR_163402.1:n.1568A>T
NM_001017524.3:c.569A>T	NP_001017524.1:p.Glu190Val