Canonical Allele Identifier: CA1400926980

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909510G= , CM000665.2:g.128909510G=	GRCh38
NC_000003.11:g.128628353G= , CM000665.1:g.128628353G=	GRCh37
NC_000003.10:g.130111043G=	NCBI36
NG_017064.1:g.35021G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+89G= MANE Select	ENSP00000312618.7:n.1563+89G=
ENST00000511325.2:n.1730G=
ENST00000679399.1:c.*1734+89G=	ENSP00000505434.1:n.*1734+89G=
ENST00000679431.1:c.*1439+89G=	ENSP00000506440.1:n.*1439+89G=
ENST00000679613.1:c.1563+89G=	ENSP00000504971.1:n.1563+89G=
ENST00000679715.1:c.1194+89G=	ENSP00000506228.1:n.1194+89G=
ENST00000679824.1:c.*2869+89G=	ENSP00000505516.1:n.*2869+89G=
ENST00000679990.1:n.1887G=
ENST00000680636.1:c.1563+89G=	ENSP00000504886.1:n.1563+89G=
ENST00000680638.1:n.1405G=
ENST00000680744.1:c.*916+89G=	ENSP00000505243.1:n.*916+89G=
ENST00000680764.1:c.*2967+89G=	ENSP00000505126.1:n.*2967+89G=
ENST00000681319.1:n.2349+89G=
ENST00000681367.1:c.1563+89G=	ENSP00000505309.1:n.1563+89G=
ENST00000681552.1:c.1150-2997G=	ENSP00000505699.1:n.1150-2997G=
ENST00000681583.1:c.1563+89G=	ENSP00000506340.1:n.1563+89G=
ENST00000681585.1:c.*182+89G=	ENSP00000506316.1:n.*182+89G=
ENST00000681784.1:n.1730G=
ENST00000681886.1:c.*845G=	ENSP00000506500.1:n.*845G=
ENST00000308982.11:c.1563+89G=	ENSP00000312618.7:n.1563+89G=
ENST00000505867.5:c.*1363+89G=	ENSP00000425346.1:n.*1363+89G=
ENST00000508971.1:c.852+89G=	ENSP00000422683.1:n.852+89G=
ENST00000511227.5:c.*1457+89G=	ENSP00000425226.1:n.*1457+89G=
ENST00000511325.1:n.633G=
ENST00000511526.5:n.1096+89G=
NM_014049.4:c.1563+89G=	NP_054768.2:n.1563+89G=
NR_033426.1:n.1941+89G=
XM_011512742.1:c.1194+89G=	XP_011511044.1:n.1194+89G=
XM_024453484.1:c.1194+89G=	XP_024309252.1:n.1194+89G=
XM_024453485.1:c.1194+89G=	XP_024309253.1:n.1194+89G=
XR_427367.3:n.1639+89G=
NM_014049.5:c.1563+89G= MANE Select	NP_054768.2:n.1563+89G=
NR_033426.2:n.1811+89G=