Canonical Allele Identifier: CA1400924308
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128903998T= , CM000665.2:g.128903998T= GRCh38
NC_000003.11:g.128622841T= , CM000665.1:g.128622841T= GRCh37
NC_000003.10:g.130105531T= NCBI36
NG_017064.1:g.29509T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.959-64T= MANE Select ENSP00000312618.7:n.959-64T=
ENST00000511325.2:n.1037-64T=
ENST00000679399.1:c.*853-64T= ENSP00000505434.1:n.*853-64T=
ENST00000679431.1:c.*835-64T= ENSP00000506440.1:n.*835-64T=
ENST00000679613.1:c.959-64T= ENSP00000504971.1:n.959-64T=
ENST00000679715.1:c.590-64T= ENSP00000506228.1:n.590-64T=
ENST00000679824.1:c.*2265-64T= ENSP00000505516.1:n.*2265-64T=
ENST00000679990.1:n.1194-64T=
ENST00000680636.1:c.959-64T= ENSP00000504886.1:n.959-64T=
ENST00000680744.1:c.*312-64T= ENSP00000505243.1:n.*312-64T=
ENST00000680764.1:c.*2363-64T= ENSP00000505126.1:n.*2363-64T=
ENST00000681319.1:n.1037-64T=
ENST00000681367.1:c.959-64T= ENSP00000505309.1:n.959-64T=
ENST00000681552.1:c.959-64T= ENSP00000505699.1:n.959-64T=
ENST00000681583.1:c.959-64T= ENSP00000506340.1:n.959-64T=
ENST00000681585.1:c.959-64T= ENSP00000506316.1:n.959-64T=
ENST00000681589.1:n.1173-64T=
ENST00000681784.1:n.1037-64T=
ENST00000681886.1:c.*152-64T= ENSP00000506500.1:n.*152-64T=
ENST00000308982.11:c.959-64T= ENSP00000312618.7:n.959-64T=
ENST00000505192.5:c.*655-64T= ENSP00000426277.1:n.*655-64T=
ENST00000505867.5:c.*759-64T= ENSP00000425346.1:n.*759-64T=
ENST00000508971.1:c.248-64T= ENSP00000422683.1:n.248-64T=
ENST00000511227.5:c.*853-64T= ENSP00000425226.1:n.*853-64T=
ENST00000511526.5:n.464-64T=
NM_014049.4:c.959-64T= NP_054768.2:n.959-64T=
NR_033426.1:n.1337-64T=
XM_011512742.1:c.590-64T= XP_011511044.1:n.590-64T=
XR_427367.1:n.1035-64T=
XM_024453484.1:c.590-64T= XP_024309252.1:n.590-64T=
XM_024453485.1:c.590-64T= XP_024309253.1:n.590-64T=
XR_427367.3:n.1035-64T=
NM_014049.5:c.959-64T= MANE Select NP_054768.2:n.959-64T=
NR_033426.2:n.1207-64T=