Canonical Allele Identifier: CA435591270

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128621413C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902570C>A , CM000665.2:g.128902570C>A	GRCh38
NC_000003.11:g.128621413C>A , CM000665.1:g.128621413C>A	GRCh37
NC_000003.10:g.130104103C>A	NCBI36
NG_017064.1:g.28081C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.900C>A MANE Select	ENSP00000312618.7:p.Leu300=
ENST00000511325.2:n.978C>A
ENST00000679399.1:c.*794C>A	ENSP00000505434.1:n.*794C>A
ENST00000679431.1:c.*772C>A	ENSP00000506440.1:n.*772C>A
ENST00000679613.1:c.900C>A	ENSP00000504971.1:p.Leu300=
ENST00000679715.1:c.531C>A	ENSP00000506228.1:p.Leu177=
ENST00000679824.1:c.*2206C>A	ENSP00000505516.1:n.*2206C>A
ENST00000679990.1:n.1135C>A
ENST00000680636.1:c.900C>A	ENSP00000504886.1:p.Leu300=
ENST00000680744.1:c.*253C>A	ENSP00000505243.1:n.*253C>A
ENST00000680764.1:c.*2300C>A	ENSP00000505126.1:n.*2300C>A
ENST00000681319.1:n.978C>A
ENST00000681367.1:c.900C>A	ENSP00000505309.1:p.Leu300=
ENST00000681552.1:c.900C>A	ENSP00000505699.1:p.Leu300=
ENST00000681583.1:c.900C>A	ENSP00000506340.1:p.Leu300=
ENST00000681585.1:c.900C>A	ENSP00000506316.1:p.Leu300=
ENST00000681589.1:n.1114C>A
ENST00000681784.1:n.978C>A
ENST00000681886.1:c.*93C>A	ENSP00000506500.1:n.*93C>A
ENST00000308982.11:c.900C>A	ENSP00000312618.7:p.Leu300=
ENST00000505192.5:c.*596C>A	ENSP00000426277.1:n.*596C>A
ENST00000505867.5:c.*700C>A	ENSP00000425346.1:n.*700C>A
ENST00000508971.1:c.189C>A	ENSP00000422683.1:p.Leu63=
ENST00000511227.5:c.*794C>A	ENSP00000425226.1:n.*794C>A
ENST00000511526.5:n.401C>A
NM_014049.4:c.900C>A	NP_054768.2:p.Leu300=
NR_033426.1:n.1278C>A
XM_011512742.1:c.531C>A	XP_011511044.1:p.Leu177=
XR_427367.1:n.972C>A
XM_024453484.1:c.531C>A	XP_024309252.1:p.Leu177=
XM_024453485.1:c.531C>A	XP_024309253.1:p.Leu177=
XR_427367.3:n.972C>A
NM_014049.5:c.900C>A MANE Select	NP_054768.2:p.Leu300=
NR_033426.2:n.1148C>A