Canonical Allele Identifier: CA354439209

Gene: CFAP92 ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628904A>C (hg19) ; chr3:g.128910061A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910061A>C , CM000665.2:g.128910061A>C	GRCh38
NC_000003.11:g.128628904A>C , CM000665.1:g.128628904A>C	GRCh37
NC_000003.10:g.130111594A>C	NCBI36
NG_017064.1:g.35572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*238T>G (CFAP92) MANE Select	ENSP00000496592.2:n.*238T>G
ENST00000308982.12:c.1604A>C (ACAD9) MANE Select	ENSP00000312618.7:p.Asn535Thr
ENST00000511325.2:n.2281A>C (ACAD9)
ENST00000645291.2:c.*238T>G (CFAP92)	ENSP00000496592.2:n.*238T>G
ENST00000679399.1:c.*1775A>C (ACAD9)	ENSP00000505434.1:n.*1775A>C
ENST00000679431.1:c.*1480A>C (ACAD9)	ENSP00000506440.1:n.*1480A>C
ENST00000679613.1:c.1604A>C (ACAD9)	ENSP00000504971.1:p.Asn535Thr
ENST00000679715.1:c.1235A>C (ACAD9)	ENSP00000506228.1:p.Asn412Thr
ENST00000679824.1:c.*2910A>C (ACAD9)	ENSP00000505516.1:n.*2910A>C
ENST00000679990.1:n.2438A>C (ACAD9)
ENST00000680636.1:c.1698A>C (ACAD9)	ENSP00000504886.1:p.Gln566His
ENST00000680638.1:n.1956A>C (ACAD9)
ENST00000680744.1:c.*957A>C (ACAD9)	ENSP00000505243.1:n.*957A>C
ENST00000680764.1:c.*3008A>C (ACAD9)	ENSP00000505126.1:n.*3008A>C
ENST00000681319.1:n.2390A>C (ACAD9)
ENST00000681367.1:c.1604A>C (ACAD9)	ENSP00000505309.1:p.Asn535Thr
ENST00000681552.1:c.1150-2446A>C (ACAD9)	ENSP00000505699.1:n.1150-2446A>C
ENST00000681583.1:c.1604A>C (ACAD9)	ENSP00000506340.1:p.Asn535Thr
ENST00000681585.1:c.*223A>C (ACAD9)	ENSP00000506316.1:n.*223A>C
ENST00000681784.1:n.2281A>C (ACAD9)
ENST00000681886.1:c.*1396A>C (ACAD9)	ENSP00000506500.1:n.*1396A>C
ENST00000308982.11:c.1604A>C (ACAD9)	ENSP00000312618.7:p.Asn535Thr
ENST00000505867.5:c.*1404A>C (ACAD9)	ENSP00000425346.1:n.*1404A>C
ENST00000508239.1:c.*238T>G	ENSP00000424951.1:n.*238T>G
ENST00000508971.1:c.893A>C (ACAD9)	ENSP00000422683.1:p.Asn298Thr
ENST00000511227.5:c.*1498A>C (ACAD9)	ENSP00000425226.1:n.*1498A>C
ENST00000511325.1:n.1184A>C (ACAD9)
ENST00000511438.5:c.*238T>G (CFAP92)	ENSP00000426217.1:n.*238T>G
ENST00000511526.5:n.1137A>C (ACAD9)
ENST00000620948.3:c.33A>C (ACAD9)	ENSP00000478191.1:p.Gln11His
NM_014049.4:c.1604A>C (ACAD9)	NP_054768.2:p.Asn535Thr
NR_033426.1:n.1982A>C (ACAD9)
XM_011512742.1:c.1235A>C (ACAD9)	XP_011511044.1:p.Asn412Thr
NM_001348520.1:c.*238T>G (CFAP92)	NP_001335449.1:n.*238T>G
NM_001348521.1:c.*238T>G (CFAP92)	NP_001335450.1:n.*238T>G
XM_024453484.1:c.1235A>C (ACAD9)	XP_024309252.1:p.Asn412Thr
XM_024453485.1:c.1235A>C (ACAD9)	XP_024309253.1:p.Asn412Thr
XR_427367.3:n.1680A>C (ACAD9)
NM_014049.5:c.1604A>C (ACAD9) MANE Select	NP_054768.2:p.Asn535Thr
NM_001348520.2:c.*238T>G (CFAP92)	NP_001335449.1:n.*238T>G
NM_001348521.2:c.*238T>G (CFAP92)	NP_001335450.1:n.*238T>G
NM_001394090.1:c.*238T>G (CFAP92) MANE Select	NP_001381019.1:n.*238T>G
NR_033426.2:n.1852A>C (ACAD9)