Canonical Allele Identifier: CA1400927176
Gene: CFAP92 HGNC NCBI
ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128909971G= , CM000665.2:g.128909971G= GRCh38
NC_000003.11:g.128628814G= , CM000665.1:g.128628814G= GRCh37
NC_000003.10:g.130111504G= NCBI36
NG_017064.1:g.35482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645291.3:c.*328C= (CFAP92) MANE Select ENSP00000496592.2:n.*328C=
ENST00000308982.12:c.1564-50G= (ACAD9) MANE Select ENSP00000312618.7:n.1564-50G=
ENST00000511325.2:n.2191G= (ACAD9)
ENST00000645291.2:c.*328C= (CFAP92) ENSP00000496592.2:n.*328C=
ENST00000679399.1:c.*1735-50G= (ACAD9) ENSP00000505434.1:n.*1735-50G=
ENST00000679431.1:c.*1440-50G= (ACAD9) ENSP00000506440.1:n.*1440-50G=
ENST00000679613.1:c.1564-50G= (ACAD9) ENSP00000504971.1:n.1564-50G=
ENST00000679715.1:c.1195-50G= (ACAD9) ENSP00000506228.1:n.1195-50G=
ENST00000679824.1:c.*2870-50G= (ACAD9) ENSP00000505516.1:n.*2870-50G=
ENST00000679990.1:n.2348G= (ACAD9)
ENST00000680636.1:c.1608G= (ACAD9) ENSP00000504886.1:p.Trp536=
ENST00000680638.1:n.1866G= (ACAD9)
ENST00000680744.1:c.*917-50G= (ACAD9) ENSP00000505243.1:n.*917-50G=
ENST00000680764.1:c.*2968-50G= (ACAD9) ENSP00000505126.1:n.*2968-50G=
ENST00000681319.1:n.2350-50G= (ACAD9)
ENST00000681367.1:c.1564-50G= (ACAD9) ENSP00000505309.1:n.1564-50G=
ENST00000681552.1:c.1150-2536G= (ACAD9) ENSP00000505699.1:n.1150-2536G=
ENST00000681583.1:c.1564-50G= (ACAD9) ENSP00000506340.1:n.1564-50G=
ENST00000681585.1:c.*183-50G= (ACAD9) ENSP00000506316.1:n.*183-50G=
ENST00000681784.1:n.2191G= (ACAD9)
ENST00000681886.1:c.*1306G= (ACAD9) ENSP00000506500.1:n.*1306G=
ENST00000308982.11:c.1564-50G= (ACAD9) ENSP00000312618.7:n.1564-50G=
ENST00000505867.5:c.*1364-50G= (ACAD9) ENSP00000425346.1:n.*1364-50G=
ENST00000508239.1:c.*328C= ENSP00000424951.1:n.*328C=
ENST00000508971.1:c.853-50G= (ACAD9) ENSP00000422683.1:n.853-50G=
ENST00000511227.5:c.*1458-50G= (ACAD9) ENSP00000425226.1:n.*1458-50G=
ENST00000511325.1:n.1094G= (ACAD9)
ENST00000511438.5:c.*328C= (CFAP92) ENSP00000426217.1:n.*328C=
ENST00000511526.5:n.1097-50G= (ACAD9)
NM_014049.4:c.1564-50G= (ACAD9) NP_054768.2:n.1564-50G=
NR_033426.1:n.1942-50G= (ACAD9)
XM_011512742.1:c.1195-50G= (ACAD9) XP_011511044.1:n.1195-50G=
NM_001348520.1:c.*328C= (CFAP92) NP_001335449.1:n.*328C=
NM_001348521.1:c.*328C= (CFAP92) NP_001335450.1:n.*328C=
XM_024453484.1:c.1195-50G= (ACAD9) XP_024309252.1:n.1195-50G=
XM_024453485.1:c.1195-50G= (ACAD9) XP_024309253.1:n.1195-50G=
XR_427367.3:n.1640-50G= (ACAD9)
NM_014049.5:c.1564-50G= (ACAD9) MANE Select NP_054768.2:n.1564-50G=
NM_001348520.2:c.*328C= (CFAP92) NP_001335449.1:n.*328C=
NM_001348521.2:c.*328C= (CFAP92) NP_001335450.1:n.*328C=
NM_001394090.1:c.*328C= (CFAP92) MANE Select NP_001381019.1:n.*328C=
NR_033426.2:n.1812-50G= (ACAD9)