Canonical Allele Identifier: CA354438474

Gene: ACAD9

Linked Data

• ClinVar Variation Id: 2679713
• ClinVar RCV Id: RCV003466621
• gnomAD v4: 3-128909342-A-G
• MyVariant Identifiers: chr3:g.128628185A>G (hg19) ; chr3:g.128909342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909342A>G , CM000665.2:g.128909342A>G	GRCh38
NC_000003.11:g.128628185A>G , CM000665.1:g.128628185A>G	GRCh37
NC_000003.10:g.130110875A>G	NCBI36
NG_017064.1:g.34853A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1486-2A>G MANE Select	ENSP00000312618.7:n.1486-2A>G
ENST00000511325.2:n.1564-2A>G
ENST00000679399.1:c.*1657-2A>G	ENSP00000505434.1:n.*1657-2A>G
ENST00000679431.1:c.*1362-2A>G	ENSP00000506440.1:n.*1362-2A>G
ENST00000679613.1:c.1486-2A>G	ENSP00000504971.1:n.1486-2A>G
ENST00000679715.1:c.1117-2A>G	ENSP00000506228.1:n.1117-2A>G
ENST00000679824.1:c.*2792-2A>G	ENSP00000505516.1:n.*2792-2A>G
ENST00000679990.1:n.1721-2A>G
ENST00000680636.1:c.1486-2A>G	ENSP00000504886.1:n.1486-2A>G
ENST00000680638.1:n.1239-2A>G
ENST00000680744.1:c.*839-2A>G	ENSP00000505243.1:n.*839-2A>G
ENST00000680764.1:c.*2890-2A>G	ENSP00000505126.1:n.*2890-2A>G
ENST00000681319.1:n.2272-2A>G
ENST00000681367.1:c.1486-2A>G	ENSP00000505309.1:n.1486-2A>G
ENST00000681552.1:c.1150-3165A>G	ENSP00000505699.1:n.1150-3165A>G
ENST00000681583.1:c.1486-2A>G	ENSP00000506340.1:n.1486-2A>G
ENST00000681585.1:c.*105-2A>G	ENSP00000506316.1:n.*105-2A>G
ENST00000681784.1:n.1564-2A>G
ENST00000681886.1:c.*679-2A>G	ENSP00000506500.1:n.*679-2A>G
ENST00000308982.11:c.1486-2A>G	ENSP00000312618.7:n.1486-2A>G
ENST00000505867.5:c.*1286-2A>G	ENSP00000425346.1:n.*1286-2A>G
ENST00000508971.1:c.775-2A>G	ENSP00000422683.1:n.775-2A>G
ENST00000511227.5:c.*1380-2A>G	ENSP00000425226.1:n.*1380-2A>G
ENST00000511325.1:n.467-2A>G
ENST00000511526.5:n.1019-2A>G
NM_014049.4:c.1486-2A>G	NP_054768.2:n.1486-2A>G
NR_033426.1:n.1864-2A>G
XM_011512742.1:c.1117-2A>G	XP_011511044.1:n.1117-2A>G
XM_024453484.1:c.1117-2A>G	XP_024309252.1:n.1117-2A>G
XM_024453485.1:c.1117-2A>G	XP_024309253.1:n.1117-2A>G
XR_427367.3:n.1562-2A>G
NM_014049.5:c.1486-2A>G MANE Select	NP_054768.2:n.1486-2A>G
NR_033426.2:n.1734-2A>G