Canonical Allele Identifier: CA1400926913
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128909385C= , CM000665.2:g.128909385C= GRCh38
NC_000003.11:g.128628228C= , CM000665.1:g.128628228C= GRCh37
NC_000003.10:g.130110918C= NCBI36
NG_017064.1:g.34896C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1527C= MANE Select ENSP00000312618.7:p.Gly509=
ENST00000511325.2:n.1605C=
ENST00000679399.1:c.*1698C= ENSP00000505434.1:n.*1698C=
ENST00000679431.1:c.*1403C= ENSP00000506440.1:n.*1403C=
ENST00000679613.1:c.1527C= ENSP00000504971.1:p.Gly509=
ENST00000679715.1:c.1158C= ENSP00000506228.1:p.Gly386=
ENST00000679824.1:c.*2833C= ENSP00000505516.1:n.*2833C=
ENST00000679990.1:n.1762C=
ENST00000680636.1:c.1527C= ENSP00000504886.1:p.Gly509=
ENST00000680638.1:n.1280C=
ENST00000680744.1:c.*880C= ENSP00000505243.1:n.*880C=
ENST00000680764.1:c.*2931C= ENSP00000505126.1:n.*2931C=
ENST00000681319.1:n.2313C=
ENST00000681367.1:c.1527C= ENSP00000505309.1:p.Gly509=
ENST00000681552.1:c.1150-3122C= ENSP00000505699.1:n.1150-3122C=
ENST00000681583.1:c.1527C= ENSP00000506340.1:p.Gly509=
ENST00000681585.1:c.*146C= ENSP00000506316.1:n.*146C=
ENST00000681784.1:n.1605C=
ENST00000681886.1:c.*720C= ENSP00000506500.1:n.*720C=
ENST00000308982.11:c.1527C= ENSP00000312618.7:p.Gly509=
ENST00000505867.5:c.*1327C= ENSP00000425346.1:n.*1327C=
ENST00000508971.1:c.816C= ENSP00000422683.1:p.Gly272=
ENST00000511227.5:c.*1421C= ENSP00000425226.1:n.*1421C=
ENST00000511325.1:n.508C=
ENST00000511526.5:n.1060C=
NM_014049.4:c.1527C= NP_054768.2:p.Gly509=
NR_033426.1:n.1905C=
XM_011512742.1:c.1158C= XP_011511044.1:p.Gly386=
XM_024453484.1:c.1158C= XP_024309252.1:p.Gly386=
XM_024453485.1:c.1158C= XP_024309253.1:p.Gly386=
XR_427367.3:n.1603C=
NM_014049.5:c.1527C= MANE Select NP_054768.2:p.Gly509=
NR_033426.2:n.1775C=