Canonical Allele Identifier: CA354439186

Gene: CFAP92 ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628902C>A (hg19) ; chr3:g.128910059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128910059C>A , CM000665.2:g.128910059C>A	GRCh38
NC_000003.11:g.128628902C>A , CM000665.1:g.128628902C>A	GRCh37
NC_000003.10:g.130111592C>A	NCBI36
NG_017064.1:g.35570C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.*240G>T (CFAP92) MANE Select	ENSP00000496592.2:n.*240G>T
ENST00000308982.12:c.1602C>A (ACAD9) MANE Select	ENSP00000312618.7:p.Ala534=
ENST00000511325.2:n.2279C>A (ACAD9)
ENST00000645291.2:c.*240G>T (CFAP92)	ENSP00000496592.2:n.*240G>T
ENST00000679399.1:c.*1773C>A (ACAD9)	ENSP00000505434.1:n.*1773C>A
ENST00000679431.1:c.*1478C>A (ACAD9)	ENSP00000506440.1:n.*1478C>A
ENST00000679613.1:c.1602C>A (ACAD9)	ENSP00000504971.1:p.Ala534=
ENST00000679715.1:c.1233C>A (ACAD9)	ENSP00000506228.1:p.Ala411=
ENST00000679824.1:c.*2908C>A (ACAD9)	ENSP00000505516.1:n.*2908C>A
ENST00000679990.1:n.2436C>A (ACAD9)
ENST00000680636.1:c.1696C>A (ACAD9)	ENSP00000504886.1:p.Gln566Lys
ENST00000680638.1:n.1954C>A (ACAD9)
ENST00000680744.1:c.*955C>A (ACAD9)	ENSP00000505243.1:n.*955C>A
ENST00000680764.1:c.*3006C>A (ACAD9)	ENSP00000505126.1:n.*3006C>A
ENST00000681319.1:n.2388C>A (ACAD9)
ENST00000681367.1:c.1602C>A (ACAD9)	ENSP00000505309.1:p.Ala534=
ENST00000681552.1:c.1150-2448C>A (ACAD9)	ENSP00000505699.1:n.1150-2448C>A
ENST00000681583.1:c.1602C>A (ACAD9)	ENSP00000506340.1:p.Ala534=
ENST00000681585.1:c.*221C>A (ACAD9)	ENSP00000506316.1:n.*221C>A
ENST00000681784.1:n.2279C>A (ACAD9)
ENST00000681886.1:c.*1394C>A (ACAD9)	ENSP00000506500.1:n.*1394C>A
ENST00000308982.11:c.1602C>A (ACAD9)	ENSP00000312618.7:p.Ala534=
ENST00000505867.5:c.*1402C>A (ACAD9)	ENSP00000425346.1:n.*1402C>A
ENST00000508239.1:c.*240G>T	ENSP00000424951.1:n.*240G>T
ENST00000508971.1:c.891C>A (ACAD9)	ENSP00000422683.1:p.Ala297=
ENST00000511227.5:c.*1496C>A (ACAD9)	ENSP00000425226.1:n.*1496C>A
ENST00000511325.1:n.1182C>A (ACAD9)
ENST00000511438.5:c.*240G>T (CFAP92)	ENSP00000426217.1:n.*240G>T
ENST00000511526.5:n.1135C>A (ACAD9)
ENST00000620948.3:c.31C>A (ACAD9)	ENSP00000478191.1:p.Gln11Lys
NM_014049.4:c.1602C>A (ACAD9)	NP_054768.2:p.Ala534=
NR_033426.1:n.1980C>A (ACAD9)
XM_011512742.1:c.1233C>A (ACAD9)	XP_011511044.1:p.Ala411=
NM_001348520.1:c.*240G>T (CFAP92)	NP_001335449.1:n.*240G>T
NM_001348521.1:c.*240G>T (CFAP92)	NP_001335450.1:n.*240G>T
XM_024453484.1:c.1233C>A (ACAD9)	XP_024309252.1:p.Ala411=
XM_024453485.1:c.1233C>A (ACAD9)	XP_024309253.1:p.Ala411=
XR_427367.3:n.1678C>A (ACAD9)
NM_014049.5:c.1602C>A (ACAD9) MANE Select	NP_054768.2:p.Ala534=
NM_001348520.2:c.*240G>T (CFAP92)	NP_001335449.1:n.*240G>T
NM_001348521.2:c.*240G>T (CFAP92)	NP_001335450.1:n.*240G>T
NM_001394090.1:c.*240G>T (CFAP92) MANE Select	NP_001381019.1:n.*240G>T
NR_033426.2:n.1850C>A (ACAD9)