Canonical Allele Identifier: CA1400928759
Gene: CFAP92 HGNC NCBI
ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128912342_128912357delinsCCCTGCAGCCCTGAAT , CM000665.2:g.128912342_128912357delinsCCCTGCAGCCCTGAAT GRCh38
NC_000003.11:g.128631185_128631200delinsCCCTGCAGCCCTGAAT , CM000665.1:g.128631185_128631200delinsCCCTGCAGCCCTGAAT GRCh37
NC_000003.10:g.130113875_130113890delinsCCCTGCAGCCCTGAAT NCBI36
NG_017064.1:g.37853_37868delinsCCCTGCAGCCCTGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645291.3:c.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG (CFAP92) MANE Select ENSP00000496592.2:n.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG...
ENST00000308982.12:c.1766-165_1766-150delinsCCCTGCAGCCCTGAAT (ACAD9) MANE Select ENSP00000312618.7:n.1766-165_1766-150delinsCCCTGCAGCCCTGAAT
ENST00000511325.2:n.2443-165_2443-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000637488.2:c.861-2024_861-2009delinsATTCAGGGCTGCAGGG (CFAP92)
ENST00000645291.2:c.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG (CFAP92) ENSP00000496592.2:n.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG...
ENST00000679399.1:c.*1937-165_*1937-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505434.1:n.*1937-165_*1937-150delinsCCCTGCAGCCCTGAAT...
ENST00000679431.1:c.*1642-165_*1642-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000506440.1:n.*1642-165_*1642-150delinsCCCTGCAGCCCTGAAT...
ENST00000679613.1:c.*133-165_*133-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000504971.1:n.*133-165_*133-150delinsCCCTGCAGCCCTGAAT
ENST00000679715.1:c.1397-165_1397-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000506228.1:n.1397-165_1397-150delinsCCCTGCAGCCCTGAAT
ENST00000679824.1:c.*3072-165_*3072-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505516.1:n.*3072-165_*3072-150delinsCCCTGCAGCCCTGAAT...
ENST00000679990.1:n.2600-165_2600-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000680636.1:c.1860-165_1860-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000504886.1:n.1860-165_1860-150delinsCCCTGCAGCCCTGAAT
ENST00000680638.1:n.3646_3661delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000680744.1:c.*1119-165_*1119-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505243.1:n.*1119-165_*1119-150delinsCCCTGCAGCCCTGAAT...
ENST00000680764.1:c.*3170-165_*3170-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505126.1:n.*3170-165_*3170-150delinsCCCTGCAGCCCTGAAT...
ENST00000681319.1:n.2552-165_2552-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000681367.1:c.1915-165_1915-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505309.1:n.1915-165_1915-150delinsCCCTGCAGCCCTGAAT
ENST00000681552.1:c.1150-165_1150-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000505699.1:n.1150-165_1150-150delinsCCCTGCAGCCCTGAAT
ENST00000681583.1:c.1766-165_1766-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000506340.1:n.1766-165_1766-150delinsCCCTGCAGCCCTGAAT
ENST00000681585.1:c.*385-165_*385-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000506316.1:n.*385-165_*385-150delinsCCCTGCAGCCCTGAAT
ENST00000681784.1:n.3034-165_3034-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000681886.1:c.*1558-165_*1558-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000506500.1:n.*1558-165_*1558-150delinsCCCTGCAGCCCTGAAT...
ENST00000308982.11:c.1766-165_1766-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000312618.7:n.1766-165_1766-150delinsCCCTGCAGCCCTGAAT
ENST00000505867.5:c.*1566-165_*1566-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000425346.1:n.*1566-165_*1566-150delinsCCCTGCAGCCCTGAAT...
ENST00000508239.1:c.1685-2024_1685-2009delinsATTCAGGGCTGCAGGG ENSP00000424951.1:n.1685-2024_1685-2009delinsATTCAGGGCTGCAGGG...
ENST00000508971.1:c.1055-165_1055-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000422683.1:n.1055-165_1055-150delinsCCCTGCAGCCCTGAAT
ENST00000511227.5:c.*1660-165_*1660-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000425226.1:n.*1660-165_*1660-150delinsCCCTGCAGCCCTGAAT...
ENST00000511325.1:n.1346-165_1346-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000511438.5:c.1169-2024_1169-2009delinsATTCAGGGCTGCAGGG (CFAP92) ENSP00000426217.1:n.1169-2024_1169-2009delinsATTCAGGGCTGCAGGG...
ENST00000511526.5:n.1299-165_1299-150delinsCCCTGCAGCCCTGAAT (ACAD9)
ENST00000620948.3:c.195-165_195-150delinsCCCTGCAGCCCTGAAT (ACAD9) ENSP00000478191.1:n.195-165_195-150delinsCCCTGCAGCCCTGAAT
NM_014049.4:c.1766-165_1766-150delinsCCCTGCAGCCCTGAAT (ACAD9) NP_054768.2:n.1766-165_1766-150delinsCCCTGCAGCCCTGAAT
NR_033426.1:n.2144-165_2144-150delinsCCCTGCAGCCCTGAAT (ACAD9)
XM_011512742.1:c.1397-165_1397-150delinsCCCTGCAGCCCTGAAT (ACAD9) XP_011511044.1:n.1397-165_1397-150delinsCCCTGCAGCCCTGAAT
XM_011513047.1:c.3398-2024_3398-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_011511349.1:n.3398-2024_3398-2009delinsATTCAGGGCTGCAGGG
XM_011513048.1:c.3267-2024_3267-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_011511350.1:n.3267-2024_3267-2009delinsATTCAGGGCTGCAGGG
XM_011513049.1:c.3267-2028_3267-2013delinsATTCAGGGCTGCAGGG (CFAP92) XP_011511351.1:n.3267-2028_3267-2013delinsATTCAGGGCTGCAGGG
XM_011513050.1:c.3323-2024_3323-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_011511352.1:n.3323-2024_3323-2009delinsATTCAGGGCTGCAGGG
NM_001348520.1:c.2408-2024_2408-2009delinsATTCAGGGCTGCAGGG (CFAP92) NP_001335449.1:n.2408-2024_2408-2009delinsATTCAGGGCTGCAGGG
NM_001348521.1:c.2312-2024_2312-2009delinsATTCAGGGCTGCAGGG (CFAP92) NP_001335450.1:n.2312-2024_2312-2009delinsATTCAGGGCTGCAGGG
XM_011513050.2:c.3377-2024_3377-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_011511352.2:n.3377-2024_3377-2009delinsATTCAGGGCTGCAGGG
XM_017006939.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862428.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006940.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862429.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006941.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862430.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006942.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862431.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006944.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862433.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006945.1:c.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862434.1:n.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG
XM_017006946.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862435.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006947.2:c.5733_5748delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862436.1:n.5733_5748delinsATTCAGGGCTGCAGGG
XM_017006948.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862437.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006950.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862439.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006951.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862440.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006952.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862441.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006953.2:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862442.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_017006954.1:c.1919-2024_1919-2009delinsATTCAGGGCTGCAGGG (CFAP92) XP_016862443.1:n.1919-2024_1919-2009delinsATTCAGGGCTGCAGGG
XM_024453484.1:c.1397-165_1397-150delinsCCCTGCAGCCCTGAAT (ACAD9) XP_024309252.1:n.1397-165_1397-150delinsCCCTGCAGCCCTGAAT
XM_024453485.1:c.1397-165_1397-150delinsCCCTGCAGCCCTGAAT (ACAD9) XP_024309253.1:n.1397-165_1397-150delinsCCCTGCAGCCCTGAAT
XM_024453688.1:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_024309456.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XM_024453689.1:c.*2598_*2613delinsATTCAGGGCTGCAGGG (CFAP92) XP_024309457.1:n.*2598_*2613delinsATTCAGGGCTGCAGGG
XR_427367.3:n.1842-165_1842-150delinsCCCTGCAGCCCTGAAT (ACAD9)
NM_014049.5:c.1766-165_1766-150delinsCCCTGCAGCCCTGAAT (ACAD9) MANE Select NP_054768.2:n.1766-165_1766-150delinsCCCTGCAGCCCTGAAT
NM_001348520.2:c.2408-2024_2408-2009delinsATTCAGGGCTGCAGGG (CFAP92) NP_001335449.1:n.2408-2024_2408-2009delinsATTCAGGGCTGCAGGG
NM_001348521.2:c.2312-2024_2312-2009delinsATTCAGGGCTGCAGGG (CFAP92) NP_001335450.1:n.2312-2024_2312-2009delinsATTCAGGGCTGCAGGG
NM_001394090.1:c.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG (CFAP92) MANE Select NP_001381019.1:n.3281-2024_3281-2009delinsATTCAGGGCTGCAGGG
NR_033426.2:n.2014-165_2014-150delinsCCCTGCAGCCCTGAAT (ACAD9)