Canonical Allele Identifier: CA378857823

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.218999C>A (hg19) ; chr11:g.218999C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.218999C>A , CM000673.2:g.218999C>A	GRCh38
NC_000011.9:g.218999C>A , CM000673.1:g.218999C>A	GRCh37
NC_000011.8:g.208999C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.1012G>T MANE Select	ENSP00000372191.4:p.Val338Phe
ENST00000382743.8:c.1012G>T	ENSP00000372191.4:p.Val338Phe
ENST00000524564.5:c.820G>T	ENSP00000432937.1:p.Val274Phe
ENST00000525319.5:c.769G>T	ENSP00000435464.1:p.Val257Phe
ENST00000529382.5:c.586G>T	ENSP00000437216.1:p.Val196Phe
ENST00000529937.1:c.*1418G>T	ENSP00000434747.1:n.*1418G>T
ENST00000532837.5:c.*725G>T	ENSP00000433899.1:n.*725G>T
ENST00000532956.5:c.850G>T	ENSP00000433077.1:p.Val284Phe
NM_001017524.2:c.586G>T	NP_001017524.1:p.Val196Phe
NM_012239.5:c.1012G>T	NP_036371.1:p.Val338Phe
XM_005252835.1:c.1012G>T	XP_005252892.1:p.Val338Phe
XM_011519956.1:c.586G>T	XP_011518258.1:p.Val196Phe
XM_011519957.1:c.586G>T	XP_011518259.1:p.Val196Phe
XM_011519956.2:c.586G>T	XP_011518258.1:p.Val196Phe
XM_011519957.2:c.586G>T	XP_011518259.1:p.Val196Phe
XM_017017428.1:c.586G>T	XP_016872917.1:p.Val196Phe
XM_017017429.1:c.586G>T	XP_016872918.1:p.Val196Phe
XM_017017430.2:c.586G>T	XP_016872919.1:p.Val196Phe
XM_017017431.1:c.586G>T	XP_016872920.1:p.Val196Phe
XM_024448410.1:c.586G>T	XP_024304178.1:p.Val196Phe
XR_001747817.1:n.1135G>T
NM_012239.6:c.1012G>T MANE Select	NP_036371.1:p.Val338Phe
NM_001370310.1:c.1012G>T	NP_001357239.1:p.Val338Phe
NM_001370312.1:c.820G>T	NP_001357241.1:p.Val274Phe
NM_001370314.1:c.850G>T	NP_001357243.1:p.Val284Phe
NM_001370315.1:c.769G>T	NP_001357244.1:p.Val257Phe
NM_001370316.1:c.340G>T	NP_001357245.1:p.Val114Phe
NM_001370317.1:c.196G>T	NP_001357246.1:p.Val66Phe
NM_001370318.1:c.586G>T	NP_001357247.1:p.Val196Phe
NM_001370319.1:c.586G>T	NP_001357248.1:p.Val196Phe
NM_001370320.1:c.586G>T	NP_001357249.1:p.Val196Phe
NM_001370321.1:c.586G>T	NP_001357250.1:p.Val196Phe
NM_001370322.1:c.586G>T	NP_001357251.1:p.Val196Phe
NM_001370323.1:c.586G>T	NP_001357252.1:p.Val196Phe
NM_001370324.1:c.544-2281G>T	NP_001357253.1:n.544-2281G>T
NM_001370325.1:c.544-2281G>T	NP_001357254.1:n.544-2281G>T
NR_163386.1:n.1201G>T
NR_163387.1:n.1088G>T
NR_163388.1:n.1136G>T
NR_163389.1:n.1456G>T
NR_163390.1:n.1136G>T
NR_163391.1:n.1343G>T
NR_163392.1:n.1545G>T
NR_163393.1:n.1610G>T
NR_163394.1:n.1034G>T
NR_163395.1:n.1289G>T
NR_163396.1:n.1115G>T
NR_163397.1:n.921G>T
NR_163398.1:n.1034G>T
NR_163399.1:n.1435G>T
NR_163400.1:n.969G>T
NR_163401.1:n.1524G>T
NR_163402.1:n.1585G>T
NM_001017524.3:c.586G>T	NP_001017524.1:p.Val196Phe