Canonical Allele Identifier: CA354439168

Gene: CFAP92 ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628900G>T (hg19) ; chr3:g.128910057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910057G>T , CM000665.2:g.128910057G>T	GRCh38
NC_000003.11:g.128628900G>T , CM000665.1:g.128628900G>T	GRCh37
NC_000003.10:g.130111590G>T	NCBI36
NG_017064.1:g.35568G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000645291.3:c.*242C>A (CFAP92) MANE Select	ENSP00000496592.2:n.*242C>A
ENST00000308982.12:c.1600G>T (ACAD9) MANE Select	ENSP00000312618.7:p.Ala534Ser
ENST00000511325.2:n.2277G>T (ACAD9)
ENST00000645291.2:c.*242C>A (CFAP92)	ENSP00000496592.2:n.*242C>A
ENST00000679399.1:c.*1771G>T (ACAD9)	ENSP00000505434.1:n.*1771G>T
ENST00000679431.1:c.*1476G>T (ACAD9)	ENSP00000506440.1:n.*1476G>T
ENST00000679613.1:c.1600G>T (ACAD9)	ENSP00000504971.1:p.Ala534Ser
ENST00000679715.1:c.1231G>T (ACAD9)	ENSP00000506228.1:p.Ala411Ser
ENST00000679824.1:c.*2906G>T (ACAD9)	ENSP00000505516.1:n.*2906G>T
ENST00000679990.1:n.2434G>T (ACAD9)
ENST00000680636.1:c.1694G>T (ACAD9)	ENSP00000504886.1:p.Gly565Val
ENST00000680638.1:n.1952G>T (ACAD9)
ENST00000680744.1:c.*953G>T (ACAD9)	ENSP00000505243.1:n.*953G>T
ENST00000680764.1:c.*3004G>T (ACAD9)	ENSP00000505126.1:n.*3004G>T
ENST00000681319.1:n.2386G>T (ACAD9)
ENST00000681367.1:c.1600G>T (ACAD9)	ENSP00000505309.1:p.Ala534Ser
ENST00000681552.1:c.1150-2450G>T (ACAD9)	ENSP00000505699.1:n.1150-2450G>T
ENST00000681583.1:c.1600G>T (ACAD9)	ENSP00000506340.1:p.Ala534Ser
ENST00000681585.1:c.*219G>T (ACAD9)	ENSP00000506316.1:n.*219G>T
ENST00000681784.1:n.2277G>T (ACAD9)
ENST00000681886.1:c.*1392G>T (ACAD9)	ENSP00000506500.1:n.*1392G>T
ENST00000308982.11:c.1600G>T (ACAD9)	ENSP00000312618.7:p.Ala534Ser
ENST00000505867.5:c.*1400G>T (ACAD9)	ENSP00000425346.1:n.*1400G>T
ENST00000508239.1:c.*242C>A	ENSP00000424951.1:n.*242C>A
ENST00000508971.1:c.889G>T (ACAD9)	ENSP00000422683.1:p.Ala297Ser
ENST00000511227.5:c.*1494G>T (ACAD9)	ENSP00000425226.1:n.*1494G>T
ENST00000511325.1:n.1180G>T (ACAD9)
ENST00000511438.5:c.*242C>A (CFAP92)	ENSP00000426217.1:n.*242C>A
ENST00000511526.5:n.1133G>T (ACAD9)
ENST00000620948.3:c.29G>T (ACAD9)	ENSP00000478191.1:p.Gly10Val
NM_014049.4:c.1600G>T (ACAD9)	NP_054768.2:p.Ala534Ser
NR_033426.1:n.1978G>T (ACAD9)
XM_011512742.1:c.1231G>T (ACAD9)	XP_011511044.1:p.Ala411Ser
NM_001348520.1:c.*242C>A (CFAP92)	NP_001335449.1:n.*242C>A
NM_001348521.1:c.*242C>A (CFAP92)	NP_001335450.1:n.*242C>A
XM_024453484.1:c.1231G>T (ACAD9)	XP_024309252.1:p.Ala411Ser
XM_024453485.1:c.1231G>T (ACAD9)	XP_024309253.1:p.Ala411Ser
XR_427367.3:n.1676G>T (ACAD9)
NM_014049.5:c.1600G>T (ACAD9) MANE Select	NP_054768.2:p.Ala534Ser
NM_001348520.2:c.*242C>A (CFAP92)	NP_001335449.1:n.*242C>A
NM_001348521.2:c.*242C>A (CFAP92)	NP_001335450.1:n.*242C>A
NM_001394090.1:c.*242C>A (CFAP92) MANE Select	NP_001381019.1:n.*242C>A
NR_033426.2:n.1848G>T (ACAD9)