Canonical Allele Identifier: CA1400926967

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909484A= , CM000665.2:g.128909484A=	GRCh38
NC_000003.11:g.128628327A= , CM000665.1:g.128628327A=	GRCh37
NC_000003.10:g.130111017A=	NCBI36
NG_017064.1:g.34995A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+63A= MANE Select	ENSP00000312618.7:n.1563+63A=
ENST00000511325.2:n.1704A=
ENST00000679399.1:c.*1734+63A=	ENSP00000505434.1:n.*1734+63A=
ENST00000679431.1:c.*1439+63A=	ENSP00000506440.1:n.*1439+63A=
ENST00000679613.1:c.1563+63A=	ENSP00000504971.1:n.1563+63A=
ENST00000679715.1:c.1194+63A=	ENSP00000506228.1:n.1194+63A=
ENST00000679824.1:c.*2869+63A=	ENSP00000505516.1:n.*2869+63A=
ENST00000679990.1:n.1861A=
ENST00000680636.1:c.1563+63A=	ENSP00000504886.1:n.1563+63A=
ENST00000680638.1:n.1379A=
ENST00000680744.1:c.*916+63A=	ENSP00000505243.1:n.*916+63A=
ENST00000680764.1:c.*2967+63A=	ENSP00000505126.1:n.*2967+63A=
ENST00000681319.1:n.2349+63A=
ENST00000681367.1:c.1563+63A=	ENSP00000505309.1:n.1563+63A=
ENST00000681552.1:c.1150-3023A=	ENSP00000505699.1:n.1150-3023A=
ENST00000681583.1:c.1563+63A=	ENSP00000506340.1:n.1563+63A=
ENST00000681585.1:c.*182+63A=	ENSP00000506316.1:n.*182+63A=
ENST00000681784.1:n.1704A=
ENST00000681886.1:c.*819A=	ENSP00000506500.1:n.*819A=
ENST00000308982.11:c.1563+63A=	ENSP00000312618.7:n.1563+63A=
ENST00000505867.5:c.*1363+63A=	ENSP00000425346.1:n.*1363+63A=
ENST00000508971.1:c.852+63A=	ENSP00000422683.1:n.852+63A=
ENST00000511227.5:c.*1457+63A=	ENSP00000425226.1:n.*1457+63A=
ENST00000511325.1:n.607A=
ENST00000511526.5:n.1096+63A=
NM_014049.4:c.1563+63A=	NP_054768.2:n.1563+63A=
NR_033426.1:n.1941+63A=
XM_011512742.1:c.1194+63A=	XP_011511044.1:n.1194+63A=
XM_024453484.1:c.1194+63A=	XP_024309252.1:n.1194+63A=
XM_024453485.1:c.1194+63A=	XP_024309253.1:n.1194+63A=
XR_427367.3:n.1639+63A=
NM_014049.5:c.1563+63A= MANE Select	NP_054768.2:n.1563+63A=
NR_033426.2:n.1811+63A=