Canonical Allele Identifier: CA1400928946

Gene: CFAP92 ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128912560G= , CM000665.2:g.128912560G=	GRCh38
NC_000003.11:g.128631403G= , CM000665.1:g.128631403G=	GRCh37
NC_000003.10:g.130114093G=	NCBI36
NG_017064.1:g.38071G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.3281-2227C= (CFAP92) MANE Select	ENSP00000496592.2:n.3281-2227C=
ENST00000308982.12:c.1819G= (ACAD9) MANE Select	ENSP00000312618.7:p.Glu607=
ENST00000511325.2:n.2496G= (ACAD9)
ENST00000637488.2:c.861-2227C= (CFAP92)
ENST00000645291.2:c.3281-2227C= (CFAP92)	ENSP00000496592.2:n.3281-2227C=
ENST00000679399.1:c.*1990G= (ACAD9)	ENSP00000505434.1:n.*1990G=
ENST00000679431.1:c.*1695G= (ACAD9)	ENSP00000506440.1:n.*1695G=
ENST00000679613.1:c.*186G= (ACAD9)	ENSP00000504971.1:n.*186G=
ENST00000679715.1:c.1450G= (ACAD9)	ENSP00000506228.1:p.Glu484=
ENST00000679824.1:c.*3125G= (ACAD9)	ENSP00000505516.1:n.*3125G=
ENST00000679990.1:n.2653G= (ACAD9)
ENST00000680636.1:c.*32G= (ACAD9)	ENSP00000504886.1:n.*32G=
ENST00000680638.1:n.3864G= (ACAD9)
ENST00000680744.1:c.*1172G= (ACAD9)	ENSP00000505243.1:n.*1172G=
ENST00000680764.1:c.*3223G= (ACAD9)	ENSP00000505126.1:n.*3223G=
ENST00000681319.1:n.2605G= (ACAD9)
ENST00000681367.1:c.*36G= (ACAD9)	ENSP00000505309.1:n.*36G=
ENST00000681552.1:c.*36G= (ACAD9)	ENSP00000505699.1:n.*36G=
ENST00000681583.1:c.1819G= (ACAD9)	ENSP00000506340.1:p.Glu607=
ENST00000681585.1:c.*438G= (ACAD9)	ENSP00000506316.1:n.*438G=
ENST00000681784.1:n.3087G= (ACAD9)
ENST00000681886.1:c.*1611G= (ACAD9)	ENSP00000506500.1:n.*1611G=
ENST00000308982.11:c.1819G= (ACAD9)	ENSP00000312618.7:p.Glu607=
ENST00000505867.5:c.*1619G= (ACAD9)	ENSP00000425346.1:n.*1619G=
ENST00000508239.1:c.1685-2227C=	ENSP00000424951.1:n.1685-2227C=
ENST00000508971.1:c.1108G= (ACAD9)	ENSP00000422683.1:p.Glu370=
ENST00000511227.5:c.*1713G= (ACAD9)	ENSP00000425226.1:n.*1713G=
ENST00000511325.1:n.1399G= (ACAD9)
ENST00000511438.5:c.1169-2227C= (CFAP92)	ENSP00000426217.1:n.1169-2227C=
ENST00000511526.5:n.1352G= (ACAD9)
ENST00000620948.3:c.246G= (ACAD9)	ENSP00000478191.1:p.Leu82=
NM_014049.4:c.1819G= (ACAD9)	NP_054768.2:p.Glu607=
NR_033426.1:n.2197G= (ACAD9)
XM_011512742.1:c.1450G= (ACAD9)	XP_011511044.1:p.Glu484=
XM_011513047.1:c.3398-2227C= (CFAP92)	XP_011511349.1:n.3398-2227C=
XM_011513048.1:c.3267-2227C= (CFAP92)	XP_011511350.1:n.3267-2227C=
XM_011513049.1:c.3267-2231C= (CFAP92)	XP_011511351.1:n.3267-2231C=
XM_011513050.1:c.3323-2227C= (CFAP92)	XP_011511352.1:n.3323-2227C=
NM_001348520.1:c.2408-2227C= (CFAP92)	NP_001335449.1:n.2408-2227C=
NM_001348521.1:c.2312-2227C= (CFAP92)	NP_001335450.1:n.2312-2227C=
XM_011513050.2:c.3377-2227C= (CFAP92)	XP_011511352.2:n.3377-2227C=
XM_017006939.2:c.*2395C= (CFAP92)	XP_016862428.1:n.*2395C=
XM_017006940.2:c.*2395C= (CFAP92)	XP_016862429.1:n.*2395C=
XM_017006941.2:c.*2395C= (CFAP92)	XP_016862430.1:n.*2395C=
XM_017006942.2:c.*2395C= (CFAP92)	XP_016862431.1:n.*2395C=
XM_017006944.2:c.*2395C= (CFAP92)	XP_016862433.1:n.*2395C=
XM_017006945.1:c.3281-2227C= (CFAP92)	XP_016862434.1:n.3281-2227C=
XM_017006946.2:c.*2395C= (CFAP92)	XP_016862435.1:n.*2395C=
XM_017006947.2:c.5530C= (CFAP92)	XP_016862436.1:n.5530C=
XM_017006948.2:c.*2395C= (CFAP92)	XP_016862437.1:n.*2395C=
XM_017006950.2:c.*2395C= (CFAP92)	XP_016862439.1:n.*2395C=
XM_017006951.2:c.*2395C= (CFAP92)	XP_016862440.1:n.*2395C=
XM_017006952.2:c.*2395C= (CFAP92)	XP_016862441.1:n.*2395C=
XM_017006953.2:c.*2395C= (CFAP92)	XP_016862442.1:n.*2395C=
XM_017006954.1:c.1919-2227C= (CFAP92)	XP_016862443.1:n.1919-2227C=
XM_024453484.1:c.1450G= (ACAD9)	XP_024309252.1:p.Glu484=
XM_024453485.1:c.1450G= (ACAD9)	XP_024309253.1:p.Glu484=
XM_024453688.1:c.*2395C= (CFAP92)	XP_024309456.1:n.*2395C=
XM_024453689.1:c.*2395C= (CFAP92)	XP_024309457.1:n.*2395C=
XR_427367.3:n.1895G= (ACAD9)
NM_014049.5:c.1819G= (ACAD9) MANE Select	NP_054768.2:p.Glu607=
NM_001348520.2:c.2408-2227C= (CFAP92)	NP_001335449.1:n.2408-2227C=
NM_001348521.2:c.2312-2227C= (CFAP92)	NP_001335450.1:n.2312-2227C=
NM_001394090.1:c.3281-2227C= (CFAP92) MANE Select	NP_001381019.1:n.3281-2227C=
NR_033426.2:n.2067G= (ACAD9)