Canonical Allele Identifier: CA378857815

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.218995G>C (hg19) ; chr11:g.218995G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.218995G>C , CM000673.2:g.218995G>C	GRCh38
NC_000011.9:g.218995G>C , CM000673.1:g.218995G>C	GRCh37
NC_000011.8:g.208995G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.1016C>G MANE Select	ENSP00000372191.4:p.Pro339Arg
ENST00000382743.8:c.1016C>G	ENSP00000372191.4:p.Pro339Arg
ENST00000524564.5:c.824C>G	ENSP00000432937.1:p.Pro275Arg
ENST00000525319.5:c.773C>G	ENSP00000435464.1:p.Pro258Arg
ENST00000529382.5:c.590C>G	ENSP00000437216.1:p.Pro197Arg
ENST00000529937.1:c.*1422C>G	ENSP00000434747.1:n.*1422C>G
ENST00000532837.5:c.*729C>G	ENSP00000433899.1:n.*729C>G
ENST00000532956.5:c.854C>G	ENSP00000433077.1:p.Pro285Arg
NM_001017524.2:c.590C>G	NP_001017524.1:p.Pro197Arg
NM_012239.5:c.1016C>G	NP_036371.1:p.Pro339Arg
XM_005252835.1:c.1016C>G	XP_005252892.1:p.Pro339Arg
XM_011519956.1:c.590C>G	XP_011518258.1:p.Pro197Arg
XM_011519957.1:c.590C>G	XP_011518259.1:p.Pro197Arg
XM_011519956.2:c.590C>G	XP_011518258.1:p.Pro197Arg
XM_011519957.2:c.590C>G	XP_011518259.1:p.Pro197Arg
XM_017017428.1:c.590C>G	XP_016872917.1:p.Pro197Arg
XM_017017429.1:c.590C>G	XP_016872918.1:p.Pro197Arg
XM_017017430.2:c.590C>G	XP_016872919.1:p.Pro197Arg
XM_017017431.1:c.590C>G	XP_016872920.1:p.Pro197Arg
XM_024448410.1:c.590C>G	XP_024304178.1:p.Pro197Arg
XR_001747817.1:n.1139C>G
NM_012239.6:c.1016C>G MANE Select	NP_036371.1:p.Pro339Arg
NM_001370310.1:c.1016C>G	NP_001357239.1:p.Pro339Arg
NM_001370312.1:c.824C>G	NP_001357241.1:p.Pro275Arg
NM_001370314.1:c.854C>G	NP_001357243.1:p.Pro285Arg
NM_001370315.1:c.773C>G	NP_001357244.1:p.Pro258Arg
NM_001370316.1:c.344C>G	NP_001357245.1:p.Pro115Arg
NM_001370317.1:c.200C>G	NP_001357246.1:p.Pro67Arg
NM_001370318.1:c.590C>G	NP_001357247.1:p.Pro197Arg
NM_001370319.1:c.590C>G	NP_001357248.1:p.Pro197Arg
NM_001370320.1:c.590C>G	NP_001357249.1:p.Pro197Arg
NM_001370321.1:c.590C>G	NP_001357250.1:p.Pro197Arg
NM_001370322.1:c.590C>G	NP_001357251.1:p.Pro197Arg
NM_001370323.1:c.590C>G	NP_001357252.1:p.Pro197Arg
NM_001370324.1:c.544-2277C>G	NP_001357253.1:n.544-2277C>G
NM_001370325.1:c.544-2277C>G	NP_001357254.1:n.544-2277C>G
NR_163386.1:n.1205C>G
NR_163387.1:n.1092C>G
NR_163388.1:n.1140C>G
NR_163389.1:n.1460C>G
NR_163390.1:n.1140C>G
NR_163391.1:n.1347C>G
NR_163392.1:n.1549C>G
NR_163393.1:n.1614C>G
NR_163394.1:n.1038C>G
NR_163395.1:n.1293C>G
NR_163396.1:n.1119C>G
NR_163397.1:n.925C>G
NR_163398.1:n.1038C>G
NR_163399.1:n.1439C>G
NR_163400.1:n.973C>G
NR_163401.1:n.1528C>G
NR_163402.1:n.1589C>G
NM_001017524.3:c.590C>G	NP_001017524.1:p.Pro197Arg