Canonical Allele Identifier: CA1400926923

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909411G= , CM000665.2:g.128909411G=	GRCh38
NC_000003.11:g.128628254G= , CM000665.1:g.128628254G=	GRCh37
NC_000003.10:g.130110944G=	NCBI36
NG_017064.1:g.34922G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1553G= MANE Select	ENSP00000312618.7:p.Arg518=
ENST00000511325.2:n.1631G=
ENST00000679399.1:c.*1724G=	ENSP00000505434.1:n.*1724G=
ENST00000679431.1:c.*1429G=	ENSP00000506440.1:n.*1429G=
ENST00000679613.1:c.1553G=	ENSP00000504971.1:p.Arg518=
ENST00000679715.1:c.1184G=	ENSP00000506228.1:p.Arg395=
ENST00000679824.1:c.*2859G=	ENSP00000505516.1:n.*2859G=
ENST00000679990.1:n.1788G=
ENST00000680636.1:c.1553G=	ENSP00000504886.1:p.Arg518=
ENST00000680638.1:n.1306G=
ENST00000680744.1:c.*906G=	ENSP00000505243.1:n.*906G=
ENST00000680764.1:c.*2957G=	ENSP00000505126.1:n.*2957G=
ENST00000681319.1:n.2339G=
ENST00000681367.1:c.1553G=	ENSP00000505309.1:p.Arg518=
ENST00000681552.1:c.1150-3096G=	ENSP00000505699.1:n.1150-3096G=
ENST00000681583.1:c.1553G=	ENSP00000506340.1:p.Arg518=
ENST00000681585.1:c.*172G=	ENSP00000506316.1:n.*172G=
ENST00000681784.1:n.1631G=
ENST00000681886.1:c.*746G=	ENSP00000506500.1:n.*746G=
ENST00000308982.11:c.1553G=	ENSP00000312618.7:p.Arg518=
ENST00000505867.5:c.*1353G=	ENSP00000425346.1:n.*1353G=
ENST00000508971.1:c.842G=	ENSP00000422683.1:p.Arg281=
ENST00000511227.5:c.*1447G=	ENSP00000425226.1:n.*1447G=
ENST00000511325.1:n.534G=
ENST00000511526.5:n.1086G=
NM_014049.4:c.1553G=	NP_054768.2:p.Arg518=
NR_033426.1:n.1931G=
XM_011512742.1:c.1184G=	XP_011511044.1:p.Arg395=
XM_024453484.1:c.1184G=	XP_024309252.1:p.Arg395=
XM_024453485.1:c.1184G=	XP_024309253.1:p.Arg395=
XR_427367.3:n.1629G=
NM_014049.5:c.1553G= MANE Select	NP_054768.2:p.Arg518=
NR_033426.2:n.1801G=