Canonical Allele Identifier: CA1400927219

Gene: CFAP92 ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910062C= , CM000665.2:g.128910062C=	GRCh38
NC_000003.11:g.128628905C= , CM000665.1:g.128628905C=	GRCh37
NC_000003.10:g.130111595C=	NCBI36
NG_017064.1:g.35573C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*237G= (CFAP92) MANE Select	ENSP00000496592.2:n.*237G=
ENST00000308982.12:c.1605C= (ACAD9) MANE Select	ENSP00000312618.7:p.Asn535=
ENST00000511325.2:n.2282C= (ACAD9)
ENST00000645291.2:c.*237G= (CFAP92)	ENSP00000496592.2:n.*237G=
ENST00000679399.1:c.*1776C= (ACAD9)	ENSP00000505434.1:n.*1776C=
ENST00000679431.1:c.*1481C= (ACAD9)	ENSP00000506440.1:n.*1481C=
ENST00000679613.1:c.1605C= (ACAD9)	ENSP00000504971.1:p.Asn535=
ENST00000679715.1:c.1236C= (ACAD9)	ENSP00000506228.1:p.Asn412=
ENST00000679824.1:c.*2911C= (ACAD9)	ENSP00000505516.1:n.*2911C=
ENST00000679990.1:n.2439C= (ACAD9)
ENST00000680636.1:c.1699C= (ACAD9)	ENSP00000504886.1:p.His567=
ENST00000680638.1:n.1957C= (ACAD9)
ENST00000680744.1:c.*958C= (ACAD9)	ENSP00000505243.1:n.*958C=
ENST00000680764.1:c.*3009C= (ACAD9)	ENSP00000505126.1:n.*3009C=
ENST00000681319.1:n.2391C= (ACAD9)
ENST00000681367.1:c.1605C= (ACAD9)	ENSP00000505309.1:p.Asn535=
ENST00000681552.1:c.1150-2445C= (ACAD9)	ENSP00000505699.1:n.1150-2445C=
ENST00000681583.1:c.1605C= (ACAD9)	ENSP00000506340.1:p.Asn535=
ENST00000681585.1:c.*224C= (ACAD9)	ENSP00000506316.1:n.*224C=
ENST00000681784.1:n.2282C= (ACAD9)
ENST00000681886.1:c.*1397C= (ACAD9)	ENSP00000506500.1:n.*1397C=
ENST00000308982.11:c.1605C= (ACAD9)	ENSP00000312618.7:p.Asn535=
ENST00000505867.5:c.*1405C= (ACAD9)	ENSP00000425346.1:n.*1405C=
ENST00000508239.1:c.*237G=	ENSP00000424951.1:n.*237G=
ENST00000508971.1:c.894C= (ACAD9)	ENSP00000422683.1:p.Asn298=
ENST00000511227.5:c.*1499C= (ACAD9)	ENSP00000425226.1:n.*1499C=
ENST00000511325.1:n.1185C= (ACAD9)
ENST00000511438.5:c.*237G= (CFAP92)	ENSP00000426217.1:n.*237G=
ENST00000511526.5:n.1138C= (ACAD9)
ENST00000620948.3:c.34C= (ACAD9)	ENSP00000478191.1:p.His12=
NM_014049.4:c.1605C= (ACAD9)	NP_054768.2:p.Asn535=
NR_033426.1:n.1983C= (ACAD9)
XM_011512742.1:c.1236C= (ACAD9)	XP_011511044.1:p.Asn412=
NM_001348520.1:c.*237G= (CFAP92)	NP_001335449.1:n.*237G=
NM_001348521.1:c.*237G= (CFAP92)	NP_001335450.1:n.*237G=
XM_024453484.1:c.1236C= (ACAD9)	XP_024309252.1:p.Asn412=
XM_024453485.1:c.1236C= (ACAD9)	XP_024309253.1:p.Asn412=
XR_427367.3:n.1681C= (ACAD9)
NM_014049.5:c.1605C= (ACAD9) MANE Select	NP_054768.2:p.Asn535=
NM_001348520.2:c.*237G= (CFAP92)	NP_001335449.1:n.*237G=
NM_001348521.2:c.*237G= (CFAP92)	NP_001335450.1:n.*237G=
NM_001394090.1:c.*237G= (CFAP92) MANE Select	NP_001381019.1:n.*237G=
NR_033426.2:n.1853C= (ACAD9)