Canonical Allele Identifier: CA1400926925

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909420A= , CM000665.2:g.128909420A=	GRCh38
NC_000003.11:g.128628263A= , CM000665.1:g.128628263A=	GRCh37
NC_000003.10:g.130110953A=	NCBI36
NG_017064.1:g.34931A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1562A= MANE Select	ENSP00000312618.7:p.Lys521=
ENST00000511325.2:n.1640A=
ENST00000679399.1:c.*1733A=	ENSP00000505434.1:n.*1733A=
ENST00000679431.1:c.*1438A=	ENSP00000506440.1:n.*1438A=
ENST00000679613.1:c.1562A=	ENSP00000504971.1:p.Lys521=
ENST00000679715.1:c.1193A=	ENSP00000506228.1:p.Lys398=
ENST00000679824.1:c.*2868A=	ENSP00000505516.1:n.*2868A=
ENST00000679990.1:n.1797A=
ENST00000680636.1:c.1562A=	ENSP00000504886.1:p.Lys521=
ENST00000680638.1:n.1315A=
ENST00000680744.1:c.*915A=	ENSP00000505243.1:n.*915A=
ENST00000680764.1:c.*2966A=	ENSP00000505126.1:n.*2966A=
ENST00000681319.1:n.2348A=
ENST00000681367.1:c.1562A=	ENSP00000505309.1:p.Lys521=
ENST00000681552.1:c.1150-3087A=	ENSP00000505699.1:n.1150-3087A=
ENST00000681583.1:c.1562A=	ENSP00000506340.1:p.Lys521=
ENST00000681585.1:c.*181A=	ENSP00000506316.1:n.*181A=
ENST00000681784.1:n.1640A=
ENST00000681886.1:c.*755A=	ENSP00000506500.1:n.*755A=
ENST00000308982.11:c.1562A=	ENSP00000312618.7:p.Lys521=
ENST00000505867.5:c.*1362A=	ENSP00000425346.1:n.*1362A=
ENST00000508971.1:c.851A=	ENSP00000422683.1:p.Lys284=
ENST00000511227.5:c.*1456A=	ENSP00000425226.1:n.*1456A=
ENST00000511325.1:n.543A=
ENST00000511526.5:n.1095A=
NM_014049.4:c.1562A=	NP_054768.2:p.Lys521=
NR_033426.1:n.1940A=
XM_011512742.1:c.1193A=	XP_011511044.1:p.Lys398=
XM_024453484.1:c.1193A=	XP_024309252.1:p.Lys398=
XM_024453485.1:c.1193A=	XP_024309253.1:p.Lys398=
XR_427367.3:n.1638A=
NM_014049.5:c.1562A= MANE Select	NP_054768.2:p.Lys521=
NR_033426.2:n.1810A=