Canonical Allele Identifier: CA1400926316
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128908282C= , CM000665.2:g.128908282C= GRCh38
NC_000003.11:g.128627125C= , CM000665.1:g.128627125C= GRCh37
NC_000003.10:g.130109815C= NCBI36
NG_017064.1:g.33793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1358+18C= MANE Select ENSP00000312618.7:n.1358+18C=
ENST00000511325.2:n.1436+18C=
ENST00000679399.1:c.*1529+18C= ENSP00000505434.1:n.*1529+18C=
ENST00000679431.1:c.*1234+18C= ENSP00000506440.1:n.*1234+18C=
ENST00000679613.1:c.1358+18C= ENSP00000504971.1:n.1358+18C=
ENST00000679715.1:c.989+18C= ENSP00000506228.1:n.989+18C=
ENST00000679824.1:c.*2664+18C= ENSP00000505516.1:n.*2664+18C=
ENST00000679990.1:n.1593+18C=
ENST00000680636.1:c.1358+18C= ENSP00000504886.1:n.1358+18C=
ENST00000680638.1:n.421C=
ENST00000680744.1:c.*711+18C= ENSP00000505243.1:n.*711+18C=
ENST00000680764.1:c.*2762+18C= ENSP00000505126.1:n.*2762+18C=
ENST00000681319.1:n.1454C=
ENST00000681367.1:c.1358+18C= ENSP00000505309.1:n.1358+18C=
ENST00000681552.1:c.1149+3777C= ENSP00000505699.1:n.1149+3777C=
ENST00000681583.1:c.1358+18C= ENSP00000506340.1:n.1358+18C=
ENST00000681585.1:c.1358+18C= ENSP00000506316.1:n.1358+18C=
ENST00000681784.1:n.1436+18C=
ENST00000681886.1:c.*551+18C= ENSP00000506500.1:n.*551+18C=
ENST00000308982.11:c.1358+18C= ENSP00000312618.7:n.1358+18C=
ENST00000505192.5:c.*1072C= ENSP00000426277.1:n.*1072C=
ENST00000505867.5:c.*1158+18C= ENSP00000425346.1:n.*1158+18C=
ENST00000508971.1:c.647+18C= ENSP00000422683.1:n.647+18C=
ENST00000511227.5:c.*1252+18C= ENSP00000425226.1:n.*1252+18C=
ENST00000511325.1:n.339+18C=
ENST00000511526.5:n.891+18C=
NM_014049.4:c.1358+18C= NP_054768.2:n.1358+18C=
NR_033426.1:n.1736+18C=
XM_011512742.1:c.989+18C= XP_011511044.1:n.989+18C=
XR_427367.1:n.1434+18C=
XM_024453484.1:c.989+18C= XP_024309252.1:n.989+18C=
XM_024453485.1:c.989+18C= XP_024309253.1:n.989+18C=
XR_427367.3:n.1434+18C=
NM_014049.5:c.1358+18C= MANE Select NP_054768.2:n.1358+18C=
NR_033426.2:n.1606+18C=