Canonical Allele Identifier: CA1400927216

Gene: CFAP92 ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910058C= , CM000665.2:g.128910058C=	GRCh38
NC_000003.11:g.128628901C= , CM000665.1:g.128628901C=	GRCh37
NC_000003.10:g.130111591C=	NCBI36
NG_017064.1:g.35569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*241G= (CFAP92) MANE Select	ENSP00000496592.2:n.*241G=
ENST00000308982.12:c.1601C= (ACAD9) MANE Select	ENSP00000312618.7:p.Ala534=
ENST00000511325.2:n.2278C= (ACAD9)
ENST00000645291.2:c.*241G= (CFAP92)	ENSP00000496592.2:n.*241G=
ENST00000679399.1:c.*1772C= (ACAD9)	ENSP00000505434.1:n.*1772C=
ENST00000679431.1:c.*1477C= (ACAD9)	ENSP00000506440.1:n.*1477C=
ENST00000679613.1:c.1601C= (ACAD9)	ENSP00000504971.1:p.Ala534=
ENST00000679715.1:c.1232C= (ACAD9)	ENSP00000506228.1:p.Ala411=
ENST00000679824.1:c.*2907C= (ACAD9)	ENSP00000505516.1:n.*2907C=
ENST00000679990.1:n.2435C= (ACAD9)
ENST00000680636.1:c.1695C= (ACAD9)	ENSP00000504886.1:p.Gly565=
ENST00000680638.1:n.1953C= (ACAD9)
ENST00000680744.1:c.*954C= (ACAD9)	ENSP00000505243.1:n.*954C=
ENST00000680764.1:c.*3005C= (ACAD9)	ENSP00000505126.1:n.*3005C=
ENST00000681319.1:n.2387C= (ACAD9)
ENST00000681367.1:c.1601C= (ACAD9)	ENSP00000505309.1:p.Ala534=
ENST00000681552.1:c.1150-2449C= (ACAD9)	ENSP00000505699.1:n.1150-2449C=
ENST00000681583.1:c.1601C= (ACAD9)	ENSP00000506340.1:p.Ala534=
ENST00000681585.1:c.*220C= (ACAD9)	ENSP00000506316.1:n.*220C=
ENST00000681784.1:n.2278C= (ACAD9)
ENST00000681886.1:c.*1393C= (ACAD9)	ENSP00000506500.1:n.*1393C=
ENST00000308982.11:c.1601C= (ACAD9)	ENSP00000312618.7:p.Ala534=
ENST00000505867.5:c.*1401C= (ACAD9)	ENSP00000425346.1:n.*1401C=
ENST00000508239.1:c.*241G=	ENSP00000424951.1:n.*241G=
ENST00000508971.1:c.890C= (ACAD9)	ENSP00000422683.1:p.Ala297=
ENST00000511227.5:c.*1495C= (ACAD9)	ENSP00000425226.1:n.*1495C=
ENST00000511325.1:n.1181C= (ACAD9)
ENST00000511438.5:c.*241G= (CFAP92)	ENSP00000426217.1:n.*241G=
ENST00000511526.5:n.1134C= (ACAD9)
ENST00000620948.3:c.30C= (ACAD9)	ENSP00000478191.1:p.Gly10=
NM_014049.4:c.1601C= (ACAD9)	NP_054768.2:p.Ala534=
NR_033426.1:n.1979C= (ACAD9)
XM_011512742.1:c.1232C= (ACAD9)	XP_011511044.1:p.Ala411=
NM_001348520.1:c.*241G= (CFAP92)	NP_001335449.1:n.*241G=
NM_001348521.1:c.*241G= (CFAP92)	NP_001335450.1:n.*241G=
XM_024453484.1:c.1232C= (ACAD9)	XP_024309252.1:p.Ala411=
XM_024453485.1:c.1232C= (ACAD9)	XP_024309253.1:p.Ala411=
XR_427367.3:n.1677C= (ACAD9)
NM_014049.5:c.1601C= (ACAD9) MANE Select	NP_054768.2:p.Ala534=
NM_001348520.2:c.*241G= (CFAP92)	NP_001335449.1:n.*241G=
NM_001348521.2:c.*241G= (CFAP92)	NP_001335450.1:n.*241G=
NM_001394090.1:c.*241G= (CFAP92) MANE Select	NP_001381019.1:n.*241G=
NR_033426.2:n.1849C= (ACAD9)