Canonical Allele Identifier: CA1400924360

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904129T= , CM000665.2:g.128904129T=	GRCh38
NC_000003.11:g.128622972T= , CM000665.1:g.128622972T=	GRCh37
NC_000003.10:g.130105662T=	NCBI36
NG_017064.1:g.29640T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1026T= MANE Select	ENSP00000312618.7:p.Ile342=
ENST00000511325.2:n.1104T=
ENST00000679399.1:c.*920T=	ENSP00000505434.1:n.*920T=
ENST00000679431.1:c.*902T=	ENSP00000506440.1:n.*902T=
ENST00000679613.1:c.1026T=	ENSP00000504971.1:p.Ile342=
ENST00000679715.1:c.657T=	ENSP00000506228.1:p.Ile219=
ENST00000679824.1:c.*2332T=	ENSP00000505516.1:n.*2332T=
ENST00000679990.1:n.1261T=
ENST00000680636.1:c.1026T=	ENSP00000504886.1:p.Ile342=
ENST00000680744.1:c.*379T=	ENSP00000505243.1:n.*379T=
ENST00000680764.1:c.*2430T=	ENSP00000505126.1:n.*2430T=
ENST00000681319.1:n.1104T=
ENST00000681367.1:c.1026T=	ENSP00000505309.1:p.Ile342=
ENST00000681552.1:c.1026T=	ENSP00000505699.1:p.Ile342=
ENST00000681583.1:c.1026T=	ENSP00000506340.1:p.Ile342=
ENST00000681585.1:c.1026T=	ENSP00000506316.1:p.Ile342=
ENST00000681589.1:n.1240T=
ENST00000681784.1:n.1104T=
ENST00000681886.1:c.*219T=	ENSP00000506500.1:n.*219T=
ENST00000308982.11:c.1026T=	ENSP00000312618.7:p.Ile342=
ENST00000505192.5:c.*722T=	ENSP00000426277.1:n.*722T=
ENST00000505867.5:c.*826T=	ENSP00000425346.1:n.*826T=
ENST00000508971.1:c.315T=	ENSP00000422683.1:p.Ile105=
ENST00000511227.5:c.*920T=	ENSP00000425226.1:n.*920T=
ENST00000511526.5:n.531T=
NM_014049.4:c.1026T=	NP_054768.2:p.Ile342=
NR_033426.1:n.1404T=
XM_011512742.1:c.657T=	XP_011511044.1:p.Ile219=
XR_427367.1:n.1102T=
XM_024453484.1:c.657T=	XP_024309252.1:p.Ile219=
XM_024453485.1:c.657T=	XP_024309253.1:p.Ile219=
XR_427367.3:n.1102T=
NM_014049.5:c.1026T= MANE Select	NP_054768.2:p.Ile342=
NR_033426.2:n.1274T=