Canonical Allele Identifier: CA1400926910
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128909382C= , CM000665.2:g.128909382C= GRCh38
NC_000003.11:g.128628225C= , CM000665.1:g.128628225C= GRCh37
NC_000003.10:g.130110915C= NCBI36
NG_017064.1:g.34893C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1524C= MANE Select ENSP00000312618.7:p.Phe508=
ENST00000511325.2:n.1602C=
ENST00000679399.1:c.*1695C= ENSP00000505434.1:n.*1695C=
ENST00000679431.1:c.*1400C= ENSP00000506440.1:n.*1400C=
ENST00000679613.1:c.1524C= ENSP00000504971.1:p.Phe508=
ENST00000679715.1:c.1155C= ENSP00000506228.1:p.Phe385=
ENST00000679824.1:c.*2830C= ENSP00000505516.1:n.*2830C=
ENST00000679990.1:n.1759C=
ENST00000680636.1:c.1524C= ENSP00000504886.1:p.Phe508=
ENST00000680638.1:n.1277C=
ENST00000680744.1:c.*877C= ENSP00000505243.1:n.*877C=
ENST00000680764.1:c.*2928C= ENSP00000505126.1:n.*2928C=
ENST00000681319.1:n.2310C=
ENST00000681367.1:c.1524C= ENSP00000505309.1:p.Phe508=
ENST00000681552.1:c.1150-3125C= ENSP00000505699.1:n.1150-3125C=
ENST00000681583.1:c.1524C= ENSP00000506340.1:p.Phe508=
ENST00000681585.1:c.*143C= ENSP00000506316.1:n.*143C=
ENST00000681784.1:n.1602C=
ENST00000681886.1:c.*717C= ENSP00000506500.1:n.*717C=
ENST00000308982.11:c.1524C= ENSP00000312618.7:p.Phe508=
ENST00000505867.5:c.*1324C= ENSP00000425346.1:n.*1324C=
ENST00000508971.1:c.813C= ENSP00000422683.1:p.Phe271=
ENST00000511227.5:c.*1418C= ENSP00000425226.1:n.*1418C=
ENST00000511325.1:n.505C=
ENST00000511526.5:n.1057C=
NM_014049.4:c.1524C= NP_054768.2:p.Phe508=
NR_033426.1:n.1902C=
XM_011512742.1:c.1155C= XP_011511044.1:p.Phe385=
XM_024453484.1:c.1155C= XP_024309252.1:p.Phe385=
XM_024453485.1:c.1155C= XP_024309253.1:p.Phe385=
XR_427367.3:n.1600C=
NM_014049.5:c.1524C= MANE Select NP_054768.2:p.Phe508=
NR_033426.2:n.1772C=