Canonical Allele Identifier: CA1400924373

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904161C= , CM000665.2:g.128904161C=	GRCh38
NC_000003.11:g.128623004C= , CM000665.1:g.128623004C=	GRCh37
NC_000003.10:g.130105694C=	NCBI36
NG_017064.1:g.29672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+29C= MANE Select	ENSP00000312618.7:n.1029+29C=
ENST00000511325.2:n.1107+29C=
ENST00000679399.1:c.*923+29C=	ENSP00000505434.1:n.*923+29C=
ENST00000679431.1:c.*905+29C=	ENSP00000506440.1:n.*905+29C=
ENST00000679613.1:c.1029+29C=	ENSP00000504971.1:n.1029+29C=
ENST00000679715.1:c.660+29C=	ENSP00000506228.1:n.660+29C=
ENST00000679824.1:c.*2335+29C=	ENSP00000505516.1:n.*2335+29C=
ENST00000679990.1:n.1264+29C=
ENST00000680636.1:c.1029+29C=	ENSP00000504886.1:n.1029+29C=
ENST00000680744.1:c.*382+29C=	ENSP00000505243.1:n.*382+29C=
ENST00000680764.1:c.*2433+29C=	ENSP00000505126.1:n.*2433+29C=
ENST00000681319.1:n.1107+29C=
ENST00000681367.1:c.1029+29C=	ENSP00000505309.1:n.1029+29C=
ENST00000681552.1:c.1029+29C=	ENSP00000505699.1:n.1029+29C=
ENST00000681583.1:c.1029+29C=	ENSP00000506340.1:n.1029+29C=
ENST00000681585.1:c.1029+29C=	ENSP00000506316.1:n.1029+29C=
ENST00000681589.1:n.1243+29C=
ENST00000681784.1:n.1107+29C=
ENST00000681886.1:c.*222+29C=	ENSP00000506500.1:n.*222+29C=
ENST00000308982.11:c.1029+29C=	ENSP00000312618.7:n.1029+29C=
ENST00000505192.5:c.*725+29C=	ENSP00000426277.1:n.*725+29C=
ENST00000505867.5:c.*829+29C=	ENSP00000425346.1:n.*829+29C=
ENST00000508971.1:c.318+29C=	ENSP00000422683.1:n.318+29C=
ENST00000511227.5:c.*923+29C=	ENSP00000425226.1:n.*923+29C=
ENST00000511526.5:n.534+29C=
NM_014049.4:c.1029+29C=	NP_054768.2:n.1029+29C=
NR_033426.1:n.1407+29C=
XM_011512742.1:c.660+29C=	XP_011511044.1:n.660+29C=
XR_427367.1:n.1105+29C=
XM_024453484.1:c.660+29C=	XP_024309252.1:n.660+29C=
XM_024453485.1:c.660+29C=	XP_024309253.1:n.660+29C=
XR_427367.3:n.1105+29C=
NM_014049.5:c.1029+29C= MANE Select	NP_054768.2:n.1029+29C=
NR_033426.2:n.1277+29C=