Canonical Allele Identifier: CA1400924445
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128904293G= , CM000665.2:g.128904293G= GRCh38
NC_000003.11:g.128623136G= , CM000665.1:g.128623136G= GRCh37
NC_000003.10:g.130105826G= NCBI36
NG_017064.1:g.29804G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1030-93G= MANE Select ENSP00000312618.7:n.1030-93G=
ENST00000511325.2:n.1108-93G=
ENST00000679399.1:c.*924-93G= ENSP00000505434.1:n.*924-93G=
ENST00000679431.1:c.*906-93G= ENSP00000506440.1:n.*906-93G=
ENST00000679613.1:c.1030-93G= ENSP00000504971.1:n.1030-93G=
ENST00000679715.1:c.661-93G= ENSP00000506228.1:n.661-93G=
ENST00000679824.1:c.*2336-93G= ENSP00000505516.1:n.*2336-93G=
ENST00000679990.1:n.1265-93G=
ENST00000680636.1:c.1030-93G= ENSP00000504886.1:n.1030-93G=
ENST00000680744.1:c.*383-93G= ENSP00000505243.1:n.*383-93G=
ENST00000680764.1:c.*2434-93G= ENSP00000505126.1:n.*2434-93G=
ENST00000681319.1:n.1108-93G=
ENST00000681367.1:c.1030-93G= ENSP00000505309.1:n.1030-93G=
ENST00000681552.1:c.1030-93G= ENSP00000505699.1:n.1030-93G=
ENST00000681583.1:c.1030-93G= ENSP00000506340.1:n.1030-93G=
ENST00000681585.1:c.1030-93G= ENSP00000506316.1:n.1030-93G=
ENST00000681589.1:n.1244-93G=
ENST00000681784.1:n.1108-93G=
ENST00000681886.1:c.*223-93G= ENSP00000506500.1:n.*223-93G=
ENST00000308982.11:c.1030-93G= ENSP00000312618.7:n.1030-93G=
ENST00000505192.5:c.*726-93G= ENSP00000426277.1:n.*726-93G=
ENST00000505867.5:c.*830-93G= ENSP00000425346.1:n.*830-93G=
ENST00000508971.1:c.319-93G= ENSP00000422683.1:n.319-93G=
ENST00000511227.5:c.*924-93G= ENSP00000425226.1:n.*924-93G=
ENST00000511526.5:n.535-65G=
NM_014049.4:c.1030-93G= NP_054768.2:n.1030-93G=
NR_033426.1:n.1408-93G=
XM_011512742.1:c.661-93G= XP_011511044.1:n.661-93G=
XR_427367.1:n.1106-93G=
XM_024453484.1:c.661-93G= XP_024309252.1:n.661-93G=
XM_024453485.1:c.661-93G= XP_024309253.1:n.661-93G=
XR_427367.3:n.1106-93G=
NM_014049.5:c.1030-93G= MANE Select NP_054768.2:n.1030-93G=
NR_033426.2:n.1278-93G=