Canonical Allele Identifier: CA2667561755

Gene: CFAP92 ACAD9

Linked Data

• gnomAD v4: 3-128909965-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909965C>T , CM000665.2:g.128909965C>T	GRCh38
NC_000003.11:g.128628808C>T , CM000665.1:g.128628808C>T	GRCh37
NC_000003.10:g.130111498C>T	NCBI36
NG_017064.1:g.35476C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000645291.3:c.*334G>A (CFAP92) MANE Select	ENSP00000496592.2:n.*334G>A
ENST00000308982.12:c.1564-56C>T (ACAD9) MANE Select	ENSP00000312618.7:n.1564-56C>T
ENST00000511325.2:n.2185C>T (ACAD9)
ENST00000645291.2:c.*334G>A (CFAP92)	ENSP00000496592.2:n.*334G>A
ENST00000679399.1:c.*1735-56C>T (ACAD9)	ENSP00000505434.1:n.*1735-56C>T
ENST00000679431.1:c.*1440-56C>T (ACAD9)	ENSP00000506440.1:n.*1440-56C>T
ENST00000679613.1:c.1564-56C>T (ACAD9)	ENSP00000504971.1:n.1564-56C>T
ENST00000679715.1:c.1195-56C>T (ACAD9)	ENSP00000506228.1:n.1195-56C>T
ENST00000679824.1:c.*2870-56C>T (ACAD9)	ENSP00000505516.1:n.*2870-56C>T
ENST00000679990.1:n.2342C>T (ACAD9)
ENST00000680636.1:c.1602C>T (ACAD9)	ENSP00000504886.1:p.Thr534=
ENST00000680638.1:n.1860C>T (ACAD9)
ENST00000680744.1:c.*917-56C>T (ACAD9)	ENSP00000505243.1:n.*917-56C>T
ENST00000680764.1:c.*2968-56C>T (ACAD9)	ENSP00000505126.1:n.*2968-56C>T
ENST00000681319.1:n.2350-56C>T (ACAD9)
ENST00000681367.1:c.1564-56C>T (ACAD9)	ENSP00000505309.1:n.1564-56C>T
ENST00000681552.1:c.1150-2542C>T (ACAD9)	ENSP00000505699.1:n.1150-2542C>T
ENST00000681583.1:c.1564-56C>T (ACAD9)	ENSP00000506340.1:n.1564-56C>T
ENST00000681585.1:c.*183-56C>T (ACAD9)	ENSP00000506316.1:n.*183-56C>T
ENST00000681784.1:n.2185C>T (ACAD9)
ENST00000681886.1:c.*1300C>T (ACAD9)	ENSP00000506500.1:n.*1300C>T
ENST00000308982.11:c.1564-56C>T (ACAD9)	ENSP00000312618.7:n.1564-56C>T
ENST00000505867.5:c.*1364-56C>T (ACAD9)	ENSP00000425346.1:n.*1364-56C>T
ENST00000508239.1:c.*334G>A	ENSP00000424951.1:n.*334G>A
ENST00000508971.1:c.853-56C>T (ACAD9)	ENSP00000422683.1:n.853-56C>T
ENST00000511227.5:c.*1458-56C>T (ACAD9)	ENSP00000425226.1:n.*1458-56C>T
ENST00000511325.1:n.1088C>T (ACAD9)
ENST00000511438.5:c.*334G>A (CFAP92)	ENSP00000426217.1:n.*334G>A
ENST00000511526.5:n.1097-56C>T (ACAD9)
NM_014049.4:c.1564-56C>T (ACAD9)	NP_054768.2:n.1564-56C>T
NR_033426.1:n.1942-56C>T (ACAD9)
XM_011512742.1:c.1195-56C>T (ACAD9)	XP_011511044.1:n.1195-56C>T
NM_001348520.1:c.*334G>A (CFAP92)	NP_001335449.1:n.*334G>A
NM_001348521.1:c.*334G>A (CFAP92)	NP_001335450.1:n.*334G>A
XM_024453484.1:c.1195-56C>T (ACAD9)	XP_024309252.1:n.1195-56C>T
XM_024453485.1:c.1195-56C>T (ACAD9)	XP_024309253.1:n.1195-56C>T
XR_427367.3:n.1640-56C>T (ACAD9)
NM_014049.5:c.1564-56C>T (ACAD9) MANE Select	NP_054768.2:n.1564-56C>T
NM_001348520.2:c.*334G>A (CFAP92)	NP_001335449.1:n.*334G>A
NM_001348521.2:c.*334G>A (CFAP92)	NP_001335450.1:n.*334G>A
NM_001394090.1:c.*334G>A (CFAP92) MANE Select	NP_001381019.1:n.*334G>A
NR_033426.2:n.1812-56C>T (ACAD9)