Canonical Allele Identifier: CA2667561759

Gene: CFAP92 ACAD9

Linked Data

• gnomAD v4: 3-128909976-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909976C>T , CM000665.2:g.128909976C>T	GRCh38
NC_000003.11:g.128628819C>T , CM000665.1:g.128628819C>T	GRCh37
NC_000003.10:g.130111509C>T	NCBI36
NG_017064.1:g.35487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*323G>A (CFAP92) MANE Select	ENSP00000496592.2:n.*323G>A
ENST00000308982.12:c.1564-45C>T (ACAD9) MANE Select	ENSP00000312618.7:n.1564-45C>T
ENST00000511325.2:n.2196C>T (ACAD9)
ENST00000645291.2:c.*323G>A (CFAP92)	ENSP00000496592.2:n.*323G>A
ENST00000679399.1:c.*1735-45C>T (ACAD9)	ENSP00000505434.1:n.*1735-45C>T
ENST00000679431.1:c.*1440-45C>T (ACAD9)	ENSP00000506440.1:n.*1440-45C>T
ENST00000679613.1:c.1564-45C>T (ACAD9)	ENSP00000504971.1:n.1564-45C>T
ENST00000679715.1:c.1195-45C>T (ACAD9)	ENSP00000506228.1:n.1195-45C>T
ENST00000679824.1:c.*2870-45C>T (ACAD9)	ENSP00000505516.1:n.*2870-45C>T
ENST00000679990.1:n.2353C>T (ACAD9)
ENST00000680636.1:c.1613C>T (ACAD9)	ENSP00000504886.1:p.Thr538Ile
ENST00000680638.1:n.1871C>T (ACAD9)
ENST00000680744.1:c.*917-45C>T (ACAD9)	ENSP00000505243.1:n.*917-45C>T
ENST00000680764.1:c.*2968-45C>T (ACAD9)	ENSP00000505126.1:n.*2968-45C>T
ENST00000681319.1:n.2350-45C>T (ACAD9)
ENST00000681367.1:c.1564-45C>T (ACAD9)	ENSP00000505309.1:n.1564-45C>T
ENST00000681552.1:c.1150-2531C>T (ACAD9)	ENSP00000505699.1:n.1150-2531C>T
ENST00000681583.1:c.1564-45C>T (ACAD9)	ENSP00000506340.1:n.1564-45C>T
ENST00000681585.1:c.*183-45C>T (ACAD9)	ENSP00000506316.1:n.*183-45C>T
ENST00000681784.1:n.2196C>T (ACAD9)
ENST00000681886.1:c.*1311C>T (ACAD9)	ENSP00000506500.1:n.*1311C>T
ENST00000308982.11:c.1564-45C>T (ACAD9)	ENSP00000312618.7:n.1564-45C>T
ENST00000505867.5:c.*1364-45C>T (ACAD9)	ENSP00000425346.1:n.*1364-45C>T
ENST00000508239.1:c.*323G>A	ENSP00000424951.1:n.*323G>A
ENST00000508971.1:c.853-45C>T (ACAD9)	ENSP00000422683.1:n.853-45C>T
ENST00000511227.5:c.*1458-45C>T (ACAD9)	ENSP00000425226.1:n.*1458-45C>T
ENST00000511325.1:n.1099C>T (ACAD9)
ENST00000511438.5:c.*323G>A (CFAP92)	ENSP00000426217.1:n.*323G>A
ENST00000511526.5:n.1097-45C>T (ACAD9)
NM_014049.4:c.1564-45C>T (ACAD9)	NP_054768.2:n.1564-45C>T
NR_033426.1:n.1942-45C>T (ACAD9)
XM_011512742.1:c.1195-45C>T (ACAD9)	XP_011511044.1:n.1195-45C>T
NM_001348520.1:c.*323G>A (CFAP92)	NP_001335449.1:n.*323G>A
NM_001348521.1:c.*323G>A (CFAP92)	NP_001335450.1:n.*323G>A
XM_024453484.1:c.1195-45C>T (ACAD9)	XP_024309252.1:n.1195-45C>T
XM_024453485.1:c.1195-45C>T (ACAD9)	XP_024309253.1:n.1195-45C>T
XR_427367.3:n.1640-45C>T (ACAD9)
NM_014049.5:c.1564-45C>T (ACAD9) MANE Select	NP_054768.2:n.1564-45C>T
NM_001348520.2:c.*323G>A (CFAP92)	NP_001335449.1:n.*323G>A
NM_001348521.2:c.*323G>A (CFAP92)	NP_001335450.1:n.*323G>A
NM_001394090.1:c.*323G>A (CFAP92) MANE Select	NP_001381019.1:n.*323G>A
NR_033426.2:n.1812-45C>T (ACAD9)