Canonical Allele Identifier: CA898710938

Gene: CFAP92 ACAD9

Linked Data

• dbSNP Id: rs1488208420
• gnomAD v3: 3-128912415-GCTGA-G
• gnomAD v4: 3-128912415-GCTGA-G
• MyVariant Identifiers: chr3:g.128631259_128631262del (hg19) ; chr3:g.128912416_128912419del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128912418_128912421del , CM000665.2:g.128912418_128912421del	GRCh38
NC_000003.11:g.128631261_128631264del , CM000665.1:g.128631261_128631264del	GRCh37
NC_000003.10:g.130113951_130113954del	NCBI36
NG_017064.1:g.37929_37932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645291.3:c.3281-2086_3281-2083del (CFAP92) MANE Select	ENSP00000496592.2:n.3281-2086_3281-2083del
ENST00000308982.12:c.1766-89_1766-86del (ACAD9) MANE Select	ENSP00000312618.7:n.1766-89_1766-86del
ENST00000511325.2:n.2443-89_2443-86del (ACAD9)
ENST00000637488.2:c.861-2086_861-2083del (CFAP92)
ENST00000645291.2:c.3281-2086_3281-2083del (CFAP92)	ENSP00000496592.2:n.3281-2086_3281-2083del
ENST00000679399.1:c.*1937-89_*1937-86del (ACAD9)	ENSP00000505434.1:n.*1937-89_*1937-86del
ENST00000679431.1:c.*1642-89_*1642-86del (ACAD9)	ENSP00000506440.1:n.*1642-89_*1642-86del
ENST00000679613.1:c.*133-89_*133-86del (ACAD9)	ENSP00000504971.1:n.*133-89_*133-86del
ENST00000679715.1:c.1397-89_1397-86del (ACAD9)	ENSP00000506228.1:n.1397-89_1397-86del
ENST00000679824.1:c.*3072-89_*3072-86del (ACAD9)	ENSP00000505516.1:n.*3072-89_*3072-86del
ENST00000679990.1:n.2600-89_2600-86del (ACAD9)
ENST00000680636.1:c.1860-89_1860-86del (ACAD9)	ENSP00000504886.1:n.1860-89_1860-86del
ENST00000680638.1:n.3722_3725del (ACAD9)
ENST00000680744.1:c.*1119-89_*1119-86del (ACAD9)	ENSP00000505243.1:n.*1119-89_*1119-86del
ENST00000680764.1:c.*3170-89_*3170-86del (ACAD9)	ENSP00000505126.1:n.*3170-89_*3170-86del
ENST00000681319.1:n.2552-89_2552-86del (ACAD9)
ENST00000681367.1:c.1915-89_1915-86del (ACAD9)	ENSP00000505309.1:n.1915-89_1915-86del
ENST00000681552.1:c.1150-89_1150-86del (ACAD9)	ENSP00000505699.1:n.1150-89_1150-86del
ENST00000681583.1:c.1766-89_1766-86del (ACAD9)	ENSP00000506340.1:n.1766-89_1766-86del
ENST00000681585.1:c.*385-89_*385-86del (ACAD9)	ENSP00000506316.1:n.*385-89_*385-86del
ENST00000681784.1:n.3034-89_3034-86del (ACAD9)
ENST00000681886.1:c.*1558-89_*1558-86del (ACAD9)	ENSP00000506500.1:n.*1558-89_*1558-86del
ENST00000308982.11:c.1766-89_1766-86del (ACAD9)	ENSP00000312618.7:n.1766-89_1766-86del
ENST00000505867.5:c.*1566-89_*1566-86del (ACAD9)	ENSP00000425346.1:n.*1566-89_*1566-86del
ENST00000508239.1:c.1685-2086_1685-2083del	ENSP00000424951.1:n.1685-2086_1685-2083del
ENST00000508971.1:c.1055-89_1055-86del (ACAD9)	ENSP00000422683.1:n.1055-89_1055-86del
ENST00000511227.5:c.*1660-89_*1660-86del (ACAD9)	ENSP00000425226.1:n.*1660-89_*1660-86del
ENST00000511325.1:n.1346-89_1346-86del (ACAD9)
ENST00000511438.5:c.1169-2086_1169-2083del (CFAP92)	ENSP00000426217.1:n.1169-2086_1169-2083del
ENST00000511526.5:n.1299-89_1299-86del (ACAD9)
ENST00000620948.3:c.195-89_195-86del (ACAD9)	ENSP00000478191.1:n.195-89_195-86del
NM_014049.4:c.1766-89_1766-86del (ACAD9)	NP_054768.2:n.1766-89_1766-86del
NR_033426.1:n.2144-89_2144-86del (ACAD9)
XM_011512742.1:c.1397-89_1397-86del (ACAD9)	XP_011511044.1:n.1397-89_1397-86del
XM_011513047.1:c.3398-2086_3398-2083del (CFAP92)	XP_011511349.1:n.3398-2086_3398-2083del
XM_011513048.1:c.3267-2086_3267-2083del (CFAP92)	XP_011511350.1:n.3267-2086_3267-2083del
XM_011513049.1:c.3267-2090_3267-2087del (CFAP92)	XP_011511351.1:n.3267-2090_3267-2087del
XM_011513050.1:c.3323-2086_3323-2083del (CFAP92)	XP_011511352.1:n.3323-2086_3323-2083del
NM_001348520.1:c.2408-2086_2408-2083del (CFAP92)	NP_001335449.1:n.2408-2086_2408-2083del
NM_001348521.1:c.2312-2086_2312-2083del (CFAP92)	NP_001335450.1:n.2312-2086_2312-2083del
XM_011513050.2:c.3377-2086_3377-2083del (CFAP92)	XP_011511352.2:n.3377-2086_3377-2083del
XM_017006939.2:c.*2536_*2539del (CFAP92)	XP_016862428.1:n.*2536_*2539del
XM_017006940.2:c.*2536_*2539del (CFAP92)	XP_016862429.1:n.*2536_*2539del
XM_017006941.2:c.*2536_*2539del (CFAP92)	XP_016862430.1:n.*2536_*2539del
XM_017006942.2:c.*2536_*2539del (CFAP92)	XP_016862431.1:n.*2536_*2539del
XM_017006944.2:c.*2536_*2539del (CFAP92)	XP_016862433.1:n.*2536_*2539del
XM_017006945.1:c.3281-2086_3281-2083del (CFAP92)	XP_016862434.1:n.3281-2086_3281-2083del
XM_017006946.2:c.*2536_*2539del (CFAP92)	XP_016862435.1:n.*2536_*2539del
XM_017006947.2:c.5671_5674del (CFAP92)	XP_016862436.1:n.5671_5674del
XM_017006948.2:c.*2536_*2539del (CFAP92)	XP_016862437.1:n.*2536_*2539del
XM_017006950.2:c.*2536_*2539del (CFAP92)	XP_016862439.1:n.*2536_*2539del
XM_017006951.2:c.*2536_*2539del (CFAP92)	XP_016862440.1:n.*2536_*2539del
XM_017006952.2:c.*2536_*2539del (CFAP92)	XP_016862441.1:n.*2536_*2539del
XM_017006953.2:c.*2536_*2539del (CFAP92)	XP_016862442.1:n.*2536_*2539del
XM_017006954.1:c.1919-2086_1919-2083del (CFAP92)	XP_016862443.1:n.1919-2086_1919-2083del
XM_024453484.1:c.1397-89_1397-86del (ACAD9)	XP_024309252.1:n.1397-89_1397-86del
XM_024453485.1:c.1397-89_1397-86del (ACAD9)	XP_024309253.1:n.1397-89_1397-86del
XM_024453688.1:c.*2536_*2539del (CFAP92)	XP_024309456.1:n.*2536_*2539del
XM_024453689.1:c.*2536_*2539del (CFAP92)	XP_024309457.1:n.*2536_*2539del
XR_427367.3:n.1842-89_1842-86del (ACAD9)
NM_014049.5:c.1766-89_1766-86del (ACAD9) MANE Select	NP_054768.2:n.1766-89_1766-86del
NM_001348520.2:c.2408-2086_2408-2083del (CFAP92)	NP_001335449.1:n.2408-2086_2408-2083del
NM_001348521.2:c.2312-2086_2312-2083del (CFAP92)	NP_001335450.1:n.2312-2086_2312-2083del
NM_001394090.1:c.3281-2086_3281-2083del (CFAP92) MANE Select	NP_001381019.1:n.3281-2086_3281-2083del
NR_033426.2:n.2014-89_2014-86del (ACAD9)