Canonical Allele Identifier: CA354439232

Gene: CFAP92 ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628907T>A (hg19) ; chr3:g.128910064T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910064T>A , CM000665.2:g.128910064T>A	GRCh38
NC_000003.11:g.128628907T>A , CM000665.1:g.128628907T>A	GRCh37
NC_000003.10:g.130111597T>A	NCBI36
NG_017064.1:g.35575T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*235A>T (CFAP92) MANE Select	ENSP00000496592.2:n.*235A>T
ENST00000308982.12:c.1607T>A (ACAD9) MANE Select	ENSP00000312618.7:p.Ile536Asn
ENST00000511325.2:n.2284T>A (ACAD9)
ENST00000645291.2:c.*235A>T (CFAP92)	ENSP00000496592.2:n.*235A>T
ENST00000679399.1:c.*1778T>A (ACAD9)	ENSP00000505434.1:n.*1778T>A
ENST00000679431.1:c.*1483T>A (ACAD9)	ENSP00000506440.1:n.*1483T>A
ENST00000679613.1:c.1607T>A (ACAD9)	ENSP00000504971.1:p.Ile536Asn
ENST00000679715.1:c.1238T>A (ACAD9)	ENSP00000506228.1:p.Ile413Asn
ENST00000679824.1:c.*2913T>A (ACAD9)	ENSP00000505516.1:n.*2913T>A
ENST00000679990.1:n.2441T>A (ACAD9)
ENST00000680636.1:c.1701T>A (ACAD9)	ENSP00000504886.1:p.His567Gln
ENST00000680638.1:n.1959T>A (ACAD9)
ENST00000680744.1:c.*960T>A (ACAD9)	ENSP00000505243.1:n.*960T>A
ENST00000680764.1:c.*3011T>A (ACAD9)	ENSP00000505126.1:n.*3011T>A
ENST00000681319.1:n.2393T>A (ACAD9)
ENST00000681367.1:c.1607T>A (ACAD9)	ENSP00000505309.1:p.Ile536Asn
ENST00000681552.1:c.1150-2443T>A (ACAD9)	ENSP00000505699.1:n.1150-2443T>A
ENST00000681583.1:c.1607T>A (ACAD9)	ENSP00000506340.1:p.Ile536Asn
ENST00000681585.1:c.*226T>A (ACAD9)	ENSP00000506316.1:n.*226T>A
ENST00000681784.1:n.2284T>A (ACAD9)
ENST00000681886.1:c.*1399T>A (ACAD9)	ENSP00000506500.1:n.*1399T>A
ENST00000308982.11:c.1607T>A (ACAD9)	ENSP00000312618.7:p.Ile536Asn
ENST00000505867.5:c.*1407T>A (ACAD9)	ENSP00000425346.1:n.*1407T>A
ENST00000508239.1:c.*235A>T	ENSP00000424951.1:n.*235A>T
ENST00000508971.1:c.896T>A (ACAD9)	ENSP00000422683.1:p.Ile299Asn
ENST00000511227.5:c.*1501T>A (ACAD9)	ENSP00000425226.1:n.*1501T>A
ENST00000511325.1:n.1187T>A (ACAD9)
ENST00000511438.5:c.*235A>T (CFAP92)	ENSP00000426217.1:n.*235A>T
ENST00000511526.5:n.1140T>A (ACAD9)
ENST00000620948.3:c.36T>A (ACAD9)	ENSP00000478191.1:p.His12Gln
NM_014049.4:c.1607T>A (ACAD9)	NP_054768.2:p.Ile536Asn
NR_033426.1:n.1985T>A (ACAD9)
XM_011512742.1:c.1238T>A (ACAD9)	XP_011511044.1:p.Ile413Asn
NM_001348520.1:c.*235A>T (CFAP92)	NP_001335449.1:n.*235A>T
NM_001348521.1:c.*235A>T (CFAP92)	NP_001335450.1:n.*235A>T
XM_024453484.1:c.1238T>A (ACAD9)	XP_024309252.1:p.Ile413Asn
XM_024453485.1:c.1238T>A (ACAD9)	XP_024309253.1:p.Ile413Asn
XR_427367.3:n.1683T>A (ACAD9)
NM_014049.5:c.1607T>A (ACAD9) MANE Select	NP_054768.2:p.Ile536Asn
NM_001348520.2:c.*235A>T (CFAP92)	NP_001335449.1:n.*235A>T
NM_001348521.2:c.*235A>T (CFAP92)	NP_001335450.1:n.*235A>T
NM_001394090.1:c.*235A>T (CFAP92) MANE Select	NP_001381019.1:n.*235A>T
NR_033426.2:n.1855T>A (ACAD9)