Canonical Allele Identifier: CA378857851

Gene: SIRT3

Linked Data

• MyVariant Identifiers: chr11:g.219015C>G (hg19) ; chr11:g.219015C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.219015C>G , CM000673.2:g.219015C>G	GRCh38
NC_000011.9:g.219015C>G , CM000673.1:g.219015C>G	GRCh37
NC_000011.8:g.209015C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382743.9:c.996G>C MANE Select	ENSP00000372191.4:p.Glu332Asp
ENST00000382743.8:c.996G>C	ENSP00000372191.4:p.Glu332Asp
ENST00000524564.5:c.804G>C	ENSP00000432937.1:p.Glu268Asp
ENST00000525319.5:c.753G>C	ENSP00000435464.1:p.Glu251Asp
ENST00000529382.5:c.570G>C	ENSP00000437216.1:p.Glu190Asp
ENST00000529937.1:c.*1402G>C	ENSP00000434747.1:n.*1402G>C
ENST00000532837.5:c.*709G>C	ENSP00000433899.1:n.*709G>C
ENST00000532956.5:c.834G>C	ENSP00000433077.1:p.Glu278Asp
NM_001017524.2:c.570G>C	NP_001017524.1:p.Glu190Asp
NM_012239.5:c.996G>C	NP_036371.1:p.Glu332Asp
XM_005252835.1:c.996G>C	XP_005252892.1:p.Glu332Asp
XM_011519956.1:c.570G>C	XP_011518258.1:p.Glu190Asp
XM_011519957.1:c.570G>C	XP_011518259.1:p.Glu190Asp
XM_011519956.2:c.570G>C	XP_011518258.1:p.Glu190Asp
XM_011519957.2:c.570G>C	XP_011518259.1:p.Glu190Asp
XM_017017428.1:c.570G>C	XP_016872917.1:p.Glu190Asp
XM_017017429.1:c.570G>C	XP_016872918.1:p.Glu190Asp
XM_017017430.2:c.570G>C	XP_016872919.1:p.Glu190Asp
XM_017017431.1:c.570G>C	XP_016872920.1:p.Glu190Asp
XM_024448410.1:c.570G>C	XP_024304178.1:p.Glu190Asp
XR_001747817.1:n.1119G>C
NM_012239.6:c.996G>C MANE Select	NP_036371.1:p.Glu332Asp
NM_001370310.1:c.996G>C	NP_001357239.1:p.Glu332Asp
NM_001370312.1:c.804G>C	NP_001357241.1:p.Glu268Asp
NM_001370314.1:c.834G>C	NP_001357243.1:p.Glu278Asp
NM_001370315.1:c.753G>C	NP_001357244.1:p.Glu251Asp
NM_001370316.1:c.324G>C	NP_001357245.1:p.Glu108Asp
NM_001370317.1:c.180G>C	NP_001357246.1:p.Glu60Asp
NM_001370318.1:c.570G>C	NP_001357247.1:p.Glu190Asp
NM_001370319.1:c.570G>C	NP_001357248.1:p.Glu190Asp
NM_001370320.1:c.570G>C	NP_001357249.1:p.Glu190Asp
NM_001370321.1:c.570G>C	NP_001357250.1:p.Glu190Asp
NM_001370322.1:c.570G>C	NP_001357251.1:p.Glu190Asp
NM_001370323.1:c.570G>C	NP_001357252.1:p.Glu190Asp
NM_001370324.1:c.544-2297G>C	NP_001357253.1:n.544-2297G>C
NM_001370325.1:c.544-2297G>C	NP_001357254.1:n.544-2297G>C
NR_163386.1:n.1185G>C
NR_163387.1:n.1072G>C
NR_163388.1:n.1120G>C
NR_163389.1:n.1440G>C
NR_163390.1:n.1120G>C
NR_163391.1:n.1327G>C
NR_163392.1:n.1529G>C
NR_163393.1:n.1594G>C
NR_163394.1:n.1018G>C
NR_163395.1:n.1273G>C
NR_163396.1:n.1099G>C
NR_163397.1:n.905G>C
NR_163398.1:n.1018G>C
NR_163399.1:n.1419G>C
NR_163400.1:n.953G>C
NR_163401.1:n.1508G>C
NR_163402.1:n.1569G>C
NM_001017524.3:c.570G>C	NP_001017524.1:p.Glu190Asp