Canonical Allele Identifier: CA1400923667
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128902597C= , CM000665.2:g.128902597C= GRCh38
NC_000003.11:g.128621440C= , CM000665.1:g.128621440C= GRCh37
NC_000003.10:g.130104130C= NCBI36
NG_017064.1:g.28108C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.927C= MANE Select ENSP00000312618.7:p.Ser309=
ENST00000511325.2:n.1005C=
ENST00000679399.1:c.*821C= ENSP00000505434.1:n.*821C=
ENST00000679431.1:c.*799C= ENSP00000506440.1:n.*799C=
ENST00000679613.1:c.927C= ENSP00000504971.1:p.Ser309=
ENST00000679715.1:c.558C= ENSP00000506228.1:p.Ser186=
ENST00000679824.1:c.*2233C= ENSP00000505516.1:n.*2233C=
ENST00000679990.1:n.1162C=
ENST00000680636.1:c.927C= ENSP00000504886.1:p.Ser309=
ENST00000680744.1:c.*280C= ENSP00000505243.1:n.*280C=
ENST00000680764.1:c.*2327C= ENSP00000505126.1:n.*2327C=
ENST00000681319.1:n.1005C=
ENST00000681367.1:c.927C= ENSP00000505309.1:p.Ser309=
ENST00000681552.1:c.927C= ENSP00000505699.1:p.Ser309=
ENST00000681583.1:c.927C= ENSP00000506340.1:p.Ser309=
ENST00000681585.1:c.927C= ENSP00000506316.1:p.Ser309=
ENST00000681589.1:n.1141C=
ENST00000681784.1:n.1005C=
ENST00000681886.1:c.*120C= ENSP00000506500.1:n.*120C=
ENST00000308982.11:c.927C= ENSP00000312618.7:p.Ser309=
ENST00000505192.5:c.*623C= ENSP00000426277.1:n.*623C=
ENST00000505867.5:c.*727C= ENSP00000425346.1:n.*727C=
ENST00000508971.1:c.216C= ENSP00000422683.1:p.Ser72=
ENST00000511227.5:c.*821C= ENSP00000425226.1:n.*821C=
ENST00000511526.5:n.428C=
NM_014049.4:c.927C= NP_054768.2:p.Ser309=
NR_033426.1:n.1305C=
XM_011512742.1:c.558C= XP_011511044.1:p.Ser186=
XR_427367.1:n.999C=
XM_024453484.1:c.558C= XP_024309252.1:p.Ser186=
XM_024453485.1:c.558C= XP_024309253.1:p.Ser186=
XR_427367.3:n.999C=
NM_014049.5:c.927C= MANE Select NP_054768.2:p.Ser309=
NR_033426.2:n.1175C=