Canonical Allele Identifier: CA378857902

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.219040A>G (hg19) ; chr11:g.219040A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219040A>G , CM000673.2:g.219040A>G	GRCh38
NC_000011.9:g.219040A>G , CM000673.1:g.219040A>G	GRCh37
NC_000011.8:g.209040A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.971T>C MANE Select	ENSP00000372191.4:p.Val324Ala
ENST00000382743.8:c.971T>C	ENSP00000372191.4:p.Val324Ala
ENST00000524564.5:c.779T>C	ENSP00000432937.1:p.Val260Ala
ENST00000525319.5:c.728T>C	ENSP00000435464.1:p.Val243Ala
ENST00000529382.5:c.545T>C	ENSP00000437216.1:p.Val182Ala
ENST00000529937.1:c.*1377T>C	ENSP00000434747.1:n.*1377T>C
ENST00000532837.5:c.*684T>C	ENSP00000433899.1:n.*684T>C
ENST00000532956.5:c.809T>C	ENSP00000433077.1:p.Val270Ala
NM_001017524.2:c.545T>C	NP_001017524.1:p.Val182Ala
NM_012239.5:c.971T>C	NP_036371.1:p.Val324Ala
XM_005252835.1:c.971T>C	XP_005252892.1:p.Val324Ala
XM_011519956.1:c.545T>C	XP_011518258.1:p.Val182Ala
XM_011519957.1:c.545T>C	XP_011518259.1:p.Val182Ala
XM_011519956.2:c.545T>C	XP_011518258.1:p.Val182Ala
XM_011519957.2:c.545T>C	XP_011518259.1:p.Val182Ala
XM_017017428.1:c.545T>C	XP_016872917.1:p.Val182Ala
XM_017017429.1:c.545T>C	XP_016872918.1:p.Val182Ala
XM_017017430.2:c.545T>C	XP_016872919.1:p.Val182Ala
XM_017017431.1:c.545T>C	XP_016872920.1:p.Val182Ala
XM_024448410.1:c.545T>C	XP_024304178.1:p.Val182Ala
XR_001747817.1:n.1094T>C
NM_012239.6:c.971T>C MANE Select	NP_036371.1:p.Val324Ala
NM_001370310.1:c.971T>C	NP_001357239.1:p.Val324Ala
NM_001370312.1:c.779T>C	NP_001357241.1:p.Val260Ala
NM_001370314.1:c.809T>C	NP_001357243.1:p.Val270Ala
NM_001370315.1:c.728T>C	NP_001357244.1:p.Val243Ala
NM_001370316.1:c.299T>C	NP_001357245.1:p.Val100Ala
NM_001370317.1:c.155T>C	NP_001357246.1:p.Val52Ala
NM_001370318.1:c.545T>C	NP_001357247.1:p.Val182Ala
NM_001370319.1:c.545T>C	NP_001357248.1:p.Val182Ala
NM_001370320.1:c.545T>C	NP_001357249.1:p.Val182Ala
NM_001370321.1:c.545T>C	NP_001357250.1:p.Val182Ala
NM_001370322.1:c.545T>C	NP_001357251.1:p.Val182Ala
NM_001370323.1:c.545T>C	NP_001357252.1:p.Val182Ala
NM_001370324.1:c.544-2322T>C	NP_001357253.1:n.544-2322T>C
NM_001370325.1:c.544-2322T>C	NP_001357254.1:n.544-2322T>C
NR_163386.1:n.1160T>C
NR_163387.1:n.1047T>C
NR_163388.1:n.1095T>C
NR_163389.1:n.1415T>C
NR_163390.1:n.1095T>C
NR_163391.1:n.1302T>C
NR_163392.1:n.1504T>C
NR_163393.1:n.1569T>C
NR_163394.1:n.993T>C
NR_163395.1:n.1248T>C
NR_163396.1:n.1074T>C
NR_163397.1:n.880T>C
NR_163398.1:n.993T>C
NR_163399.1:n.1394T>C
NR_163400.1:n.928T>C
NR_163401.1:n.1483T>C
NR_163402.1:n.1544T>C
NM_001017524.3:c.545T>C	NP_001017524.1:p.Val182Ala