Canonical Allele Identifier: CA378857540

Gene: SIRT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.218857T>A , CM000673.2:g.218857T>A	GRCh38
NC_000011.9:g.218857T>A , CM000673.1:g.218857T>A	GRCh37
NC_000011.8:g.208857T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012239.6:c.1154A>T MANE Select	NP_036371.1:p.Asp385Val
ENST00000382743.9:c.1154A>T MANE Select	ENSP00000372191.4:p.Asp385Val
NM_001017524.2:c.728A>T	NP_001017524.1:p.Asp243Val
NM_001017524.3:c.728A>T	NP_001017524.1:p.Asp243Val
NM_001370310.1:c.1154A>T	NP_001357239.1:p.Asp385Val
NM_001370312.1:c.962A>T	NP_001357241.1:p.Asp321Val
NM_001370314.1:c.992A>T	NP_001357243.1:p.Asp331Val
NM_001370315.1:c.911A>T	NP_001357244.1:p.Asp304Val
NM_001370316.1:c.482A>T	NP_001357245.1:p.Asp161Val
NM_001370317.1:c.338A>T	NP_001357246.1:p.Asp113Val
NM_001370318.1:c.728A>T	NP_001357247.1:p.Asp243Val
NM_001370319.1:c.728A>T	NP_001357248.1:p.Asp243Val
NM_001370320.1:c.728A>T	NP_001357249.1:p.Asp243Val
NM_001370321.1:c.728A>T	NP_001357250.1:p.Asp243Val
NM_001370322.1:c.728A>T	NP_001357251.1:p.Asp243Val
NM_001370323.1:c.728A>T	NP_001357252.1:p.Asp243Val
NM_001370324.1:c.544-2139A>T	NP_001357253.1:n.544-2139A>T
NM_001370325.1:c.544-2139A>T	NP_001357254.1:n.544-2139A>T
NM_012239.5:c.1154A>T	NP_036371.1:p.Asp385Val
NR_163386.1:n.1343A>T
NR_163387.1:n.1230A>T
NR_163388.1:n.1278A>T
NR_163389.1:n.1598A>T
NR_163390.1:n.1278A>T
NR_163391.1:n.1485A>T
NR_163392.1:n.1687A>T
NR_163393.1:n.1752A>T
NR_163394.1:n.1176A>T
NR_163395.1:n.1431A>T
NR_163396.1:n.1257A>T
NR_163397.1:n.1063A>T
NR_163398.1:n.1176A>T
NR_163399.1:n.1577A>T
NR_163400.1:n.1111A>T
NR_163401.1:n.1666A>T
NR_163402.1:n.1727A>T
ENST00000382743.8:c.1154A>T	ENSP00000372191.4:p.Asp385Val
ENST00000524564.5:c.962A>T	ENSP00000432937.1:p.Asp321Val
ENST00000525319.5:c.911A>T	ENSP00000435464.1:p.Asp304Val
ENST00000529382.5:c.728A>T	ENSP00000437216.1:p.Asp243Val
ENST00000529937.1:c.*1560A>T	ENSP00000434747.1:n.*1560A>T
ENST00000532837.5:c.*867A>T	ENSP00000433899.1:n.*867A>T
ENST00000532956.5:c.992A>T	ENSP00000433077.1:p.Asp331Val
XM_005252835.1:c.1154A>T	XP_005252892.1:p.Asp385Val
XM_011519956.1:c.728A>T	XP_011518258.1:p.Asp243Val
XM_011519956.2:c.728A>T	XP_011518258.1:p.Asp243Val
XM_011519957.1:c.728A>T	XP_011518259.1:p.Asp243Val
XM_011519957.2:c.728A>T	XP_011518259.1:p.Asp243Val
XM_017017428.1:c.728A>T	XP_016872917.1:p.Asp243Val
XM_017017429.1:c.728A>T	XP_016872918.1:p.Asp243Val
XM_017017430.2:c.728A>T	XP_016872919.1:p.Asp243Val
XM_017017431.1:c.728A>T	XP_016872920.1:p.Asp243Val
XM_024448410.1:c.728A>T	XP_024304178.1:p.Asp243Val
XR_001747817.1:n.1277A>T