Canonical Allele Identifier: CA1400924385

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904188G= , CM000665.2:g.128904188G=	GRCh38
NC_000003.11:g.128623031G= , CM000665.1:g.128623031G=	GRCh37
NC_000003.10:g.130105721G=	NCBI36
NG_017064.1:g.29699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+56G= MANE Select	ENSP00000312618.7:n.1029+56G=
ENST00000511325.2:n.1107+56G=
ENST00000679399.1:c.*923+56G=	ENSP00000505434.1:n.*923+56G=
ENST00000679431.1:c.*905+56G=	ENSP00000506440.1:n.*905+56G=
ENST00000679613.1:c.1029+56G=	ENSP00000504971.1:n.1029+56G=
ENST00000679715.1:c.660+56G=	ENSP00000506228.1:n.660+56G=
ENST00000679824.1:c.*2335+56G=	ENSP00000505516.1:n.*2335+56G=
ENST00000679990.1:n.1264+56G=
ENST00000680636.1:c.1029+56G=	ENSP00000504886.1:n.1029+56G=
ENST00000680744.1:c.*382+56G=	ENSP00000505243.1:n.*382+56G=
ENST00000680764.1:c.*2433+56G=	ENSP00000505126.1:n.*2433+56G=
ENST00000681319.1:n.1107+56G=
ENST00000681367.1:c.1029+56G=	ENSP00000505309.1:n.1029+56G=
ENST00000681552.1:c.1029+56G=	ENSP00000505699.1:n.1029+56G=
ENST00000681583.1:c.1029+56G=	ENSP00000506340.1:n.1029+56G=
ENST00000681585.1:c.1029+56G=	ENSP00000506316.1:n.1029+56G=
ENST00000681589.1:n.1243+56G=
ENST00000681784.1:n.1107+56G=
ENST00000681886.1:c.*222+56G=	ENSP00000506500.1:n.*222+56G=
ENST00000308982.11:c.1029+56G=	ENSP00000312618.7:n.1029+56G=
ENST00000505192.5:c.*725+56G=	ENSP00000426277.1:n.*725+56G=
ENST00000505867.5:c.*829+56G=	ENSP00000425346.1:n.*829+56G=
ENST00000508971.1:c.318+56G=	ENSP00000422683.1:n.318+56G=
ENST00000511227.5:c.*923+56G=	ENSP00000425226.1:n.*923+56G=
ENST00000511526.5:n.534+56G=
NM_014049.4:c.1029+56G=	NP_054768.2:n.1029+56G=
NR_033426.1:n.1407+56G=
XM_011512742.1:c.660+56G=	XP_011511044.1:n.660+56G=
XR_427367.1:n.1105+56G=
XM_024453484.1:c.660+56G=	XP_024309252.1:n.660+56G=
XM_024453485.1:c.660+56G=	XP_024309253.1:n.660+56G=
XR_427367.3:n.1105+56G=
NM_014049.5:c.1029+56G= MANE Select	NP_054768.2:n.1029+56G=
NR_033426.2:n.1277+56G=