Canonical Allele Identifier: CA82542873

Gene: CFAP92 ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128912539_128912542del , CM000665.2:g.128912539_128912542del	GRCh38
NC_000003.11:g.128631382_128631385del , CM000665.1:g.128631382_128631385del	GRCh37
NC_000003.10:g.130114072_130114075del	NCBI36
NG_017064.1:g.38050_38053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.3281-2206_3281-2203del (CFAP92) MANE Select	ENSP00000496592.2:n.3281-2206_3281-2203del
ENST00000308982.12:c.1798_1801del (ACAD9) MANE Select	ENSP00000312618.7:p.Lys600CysfsTer?
ENST00000511325.2:n.2475_2478del (ACAD9)
ENST00000637488.2:c.861-2206_861-2203del (CFAP92)
ENST00000645291.2:c.3281-2206_3281-2203del (CFAP92)	ENSP00000496592.2:n.3281-2206_3281-2203del
ENST00000679399.1:c.*1969_*1972del (ACAD9)	ENSP00000505434.1:n.*1969_*1972del
ENST00000679431.1:c.*1674_*1677del (ACAD9)	ENSP00000506440.1:n.*1674_*1677del
ENST00000679613.1:c.*165_*168del (ACAD9)	ENSP00000504971.1:n.*165_*168del
ENST00000679715.1:c.1429_1432del (ACAD9)	ENSP00000506228.1:p.Lys477CysfsTer?
ENST00000679824.1:c.*3104_*3107del (ACAD9)	ENSP00000505516.1:n.*3104_*3107del
ENST00000679990.1:n.2632_2635del (ACAD9)
ENST00000680636.1:c.*11_*14del (ACAD9)	ENSP00000504886.1:n.*11_*14del
ENST00000680638.1:n.3843_3846del (ACAD9)
ENST00000680744.1:c.*1151_*1154del (ACAD9)	ENSP00000505243.1:n.*1151_*1154del
ENST00000680764.1:c.*3202_*3205del (ACAD9)	ENSP00000505126.1:n.*3202_*3205del
ENST00000681319.1:n.2584_2587del (ACAD9)
ENST00000681367.1:c.*15_*18del (ACAD9)	ENSP00000505309.1:n.*15_*18del
ENST00000681552.1:c.*15_*18del (ACAD9)	ENSP00000505699.1:n.*15_*18del
ENST00000681583.1:c.1798_1801del (ACAD9)	ENSP00000506340.1:p.Lys600CysfsTer?
ENST00000681585.1:c.*417_*420del (ACAD9)	ENSP00000506316.1:n.*417_*420del
ENST00000681784.1:n.3066_3069del (ACAD9)
ENST00000681886.1:c.*1590_*1593del (ACAD9)	ENSP00000506500.1:n.*1590_*1593del
ENST00000308982.11:c.1798_1801del (ACAD9)	ENSP00000312618.7:p.Lys600CysfsTer?
ENST00000505867.5:c.*1598_*1601del (ACAD9)	ENSP00000425346.1:n.*1598_*1601del
ENST00000508239.1:c.1685-2206_1685-2203del	ENSP00000424951.1:n.1685-2206_1685-2203del
ENST00000508971.1:c.1087_1090del (ACAD9)	ENSP00000422683.1:p.Lys363CysfsTer?
ENST00000511227.5:c.*1692_*1695del (ACAD9)	ENSP00000425226.1:n.*1692_*1695del
ENST00000511325.1:n.1378_1381del (ACAD9)
ENST00000511438.5:c.1169-2206_1169-2203del (CFAP92)	ENSP00000426217.1:n.1169-2206_1169-2203del
ENST00000511526.5:n.1331_1334del (ACAD9)
ENST00000620948.3:c.225_228del (ACAD9)	ENSP00000478191.1:p.Arg75SerfsTer7
NM_014049.4:c.1798_1801del (ACAD9)	NP_054768.2:p.Lys600CysfsTer?
NR_033426.1:n.2176_2179del (ACAD9)
XM_011512742.1:c.1429_1432del (ACAD9)	XP_011511044.1:p.Lys477CysfsTer?
XM_011513047.1:c.3398-2206_3398-2203del (CFAP92)	XP_011511349.1:n.3398-2206_3398-2203del
XM_011513048.1:c.3267-2206_3267-2203del (CFAP92)	XP_011511350.1:n.3267-2206_3267-2203del
XM_011513049.1:c.3267-2210_3267-2207del (CFAP92)	XP_011511351.1:n.3267-2210_3267-2207del
XM_011513050.1:c.3323-2206_3323-2203del (CFAP92)	XP_011511352.1:n.3323-2206_3323-2203del
NM_001348520.1:c.2408-2206_2408-2203del (CFAP92)	NP_001335449.1:n.2408-2206_2408-2203del
NM_001348521.1:c.2312-2206_2312-2203del (CFAP92)	NP_001335450.1:n.2312-2206_2312-2203del
XM_011513050.2:c.3377-2206_3377-2203del (CFAP92)	XP_011511352.2:n.3377-2206_3377-2203del
XM_017006939.2:c.*2416_*2419del (CFAP92)	XP_016862428.1:n.*2416_*2419del
XM_017006940.2:c.*2416_*2419del (CFAP92)	XP_016862429.1:n.*2416_*2419del
XM_017006941.2:c.*2416_*2419del (CFAP92)	XP_016862430.1:n.*2416_*2419del
XM_017006942.2:c.*2416_*2419del (CFAP92)	XP_016862431.1:n.*2416_*2419del
XM_017006944.2:c.*2416_*2419del (CFAP92)	XP_016862433.1:n.*2416_*2419del
XM_017006945.1:c.3281-2206_3281-2203del (CFAP92)	XP_016862434.1:n.3281-2206_3281-2203del
XM_017006946.2:c.*2416_*2419del (CFAP92)	XP_016862435.1:n.*2416_*2419del
XM_017006947.2:c.5551_5554del (CFAP92)	XP_016862436.1:n.5551_5554del
XM_017006948.2:c.*2416_*2419del (CFAP92)	XP_016862437.1:n.*2416_*2419del
XM_017006950.2:c.*2416_*2419del (CFAP92)	XP_016862439.1:n.*2416_*2419del
XM_017006951.2:c.*2416_*2419del (CFAP92)	XP_016862440.1:n.*2416_*2419del
XM_017006952.2:c.*2416_*2419del (CFAP92)	XP_016862441.1:n.*2416_*2419del
XM_017006953.2:c.*2416_*2419del (CFAP92)	XP_016862442.1:n.*2416_*2419del
XM_017006954.1:c.1919-2206_1919-2203del (CFAP92)	XP_016862443.1:n.1919-2206_1919-2203del
XM_024453484.1:c.1429_1432del (ACAD9)	XP_024309252.1:p.Lys477CysfsTer?
XM_024453485.1:c.1429_1432del (ACAD9)	XP_024309253.1:p.Lys477CysfsTer?
XM_024453688.1:c.*2416_*2419del (CFAP92)	XP_024309456.1:n.*2416_*2419del
XM_024453689.1:c.*2416_*2419del (CFAP92)	XP_024309457.1:n.*2416_*2419del
XR_427367.3:n.1874_1877del (ACAD9)
NM_014049.5:c.1798_1801del (ACAD9) MANE Select	NP_054768.2:p.Lys600CysfsTer?
NM_001348520.2:c.2408-2206_2408-2203del (CFAP92)	NP_001335449.1:n.2408-2206_2408-2203del
NM_001348521.2:c.2312-2206_2312-2203del (CFAP92)	NP_001335450.1:n.2312-2206_2312-2203del
NM_001394090.1:c.3281-2206_3281-2203del (CFAP92) MANE Select	NP_001381019.1:n.3281-2206_3281-2203del
NR_033426.2:n.2046_2049del (ACAD9)