Canonical Allele Identifier: CA435595093

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628255C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909412C>A , CM000665.2:g.128909412C>A	GRCh38
NC_000003.11:g.128628255C>A , CM000665.1:g.128628255C>A	GRCh37
NC_000003.10:g.130110945C>A	NCBI36
NG_017064.1:g.34923C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1554C>A MANE Select	ENSP00000312618.7:p.Arg518=
ENST00000511325.2:n.1632C>A
ENST00000679399.1:c.*1725C>A	ENSP00000505434.1:n.*1725C>A
ENST00000679431.1:c.*1430C>A	ENSP00000506440.1:n.*1430C>A
ENST00000679613.1:c.1554C>A	ENSP00000504971.1:p.Arg518=
ENST00000679715.1:c.1185C>A	ENSP00000506228.1:p.Arg395=
ENST00000679824.1:c.*2860C>A	ENSP00000505516.1:n.*2860C>A
ENST00000679990.1:n.1789C>A
ENST00000680636.1:c.1554C>A	ENSP00000504886.1:p.Arg518=
ENST00000680638.1:n.1307C>A
ENST00000680744.1:c.*907C>A	ENSP00000505243.1:n.*907C>A
ENST00000680764.1:c.*2958C>A	ENSP00000505126.1:n.*2958C>A
ENST00000681319.1:n.2340C>A
ENST00000681367.1:c.1554C>A	ENSP00000505309.1:p.Arg518=
ENST00000681552.1:c.1150-3095C>A	ENSP00000505699.1:n.1150-3095C>A
ENST00000681583.1:c.1554C>A	ENSP00000506340.1:p.Arg518=
ENST00000681585.1:c.*173C>A	ENSP00000506316.1:n.*173C>A
ENST00000681784.1:n.1632C>A
ENST00000681886.1:c.*747C>A	ENSP00000506500.1:n.*747C>A
ENST00000308982.11:c.1554C>A	ENSP00000312618.7:p.Arg518=
ENST00000505867.5:c.*1354C>A	ENSP00000425346.1:n.*1354C>A
ENST00000508971.1:c.843C>A	ENSP00000422683.1:p.Arg281=
ENST00000511227.5:c.*1448C>A	ENSP00000425226.1:n.*1448C>A
ENST00000511325.1:n.535C>A
ENST00000511526.5:n.1087C>A
NM_014049.4:c.1554C>A	NP_054768.2:p.Arg518=
NR_033426.1:n.1932C>A
XM_011512742.1:c.1185C>A	XP_011511044.1:p.Arg395=
XM_024453484.1:c.1185C>A	XP_024309252.1:p.Arg395=
XM_024453485.1:c.1185C>A	XP_024309253.1:p.Arg395=
XR_427367.3:n.1630C>A
NM_014049.5:c.1554C>A MANE Select	NP_054768.2:p.Arg518=
NR_033426.2:n.1802C>A