Canonical Allele Identifier: CA1400924376

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904168_128904170delinsCTG , CM000665.2:g.128904168_128904170delinsCTG	GRCh38
NC_000003.11:g.128623011_128623013delinsCTG , CM000665.1:g.128623011_128623013delinsCTG	GRCh37
NC_000003.10:g.130105701_130105703delinsCTG	NCBI36
NG_017064.1:g.29679_29681delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+36_1029+38delinsCTG MANE Select	ENSP00000312618.7:n.1029+36_1029+38delinsCTG
ENST00000511325.2:n.1107+36_1107+38delinsCTG
ENST00000679399.1:c.*923+36_*923+38delinsCTG	ENSP00000505434.1:n.*923+36_*923+38delinsCTG
ENST00000679431.1:c.*905+36_*905+38delinsCTG	ENSP00000506440.1:n.*905+36_*905+38delinsCTG
ENST00000679613.1:c.1029+36_1029+38delinsCTG	ENSP00000504971.1:n.1029+36_1029+38delinsCTG
ENST00000679715.1:c.660+36_660+38delinsCTG	ENSP00000506228.1:n.660+36_660+38delinsCTG
ENST00000679824.1:c.*2335+36_*2335+38delinsCTG	ENSP00000505516.1:n.*2335+36_*2335+38delinsCTG
ENST00000679990.1:n.1264+36_1264+38delinsCTG
ENST00000680636.1:c.1029+36_1029+38delinsCTG	ENSP00000504886.1:n.1029+36_1029+38delinsCTG
ENST00000680744.1:c.*382+36_*382+38delinsCTG	ENSP00000505243.1:n.*382+36_*382+38delinsCTG
ENST00000680764.1:c.*2433+36_*2433+38delinsCTG	ENSP00000505126.1:n.*2433+36_*2433+38delinsCTG
ENST00000681319.1:n.1107+36_1107+38delinsCTG
ENST00000681367.1:c.1029+36_1029+38delinsCTG	ENSP00000505309.1:n.1029+36_1029+38delinsCTG
ENST00000681552.1:c.1029+36_1029+38delinsCTG	ENSP00000505699.1:n.1029+36_1029+38delinsCTG
ENST00000681583.1:c.1029+36_1029+38delinsCTG	ENSP00000506340.1:n.1029+36_1029+38delinsCTG
ENST00000681585.1:c.1029+36_1029+38delinsCTG	ENSP00000506316.1:n.1029+36_1029+38delinsCTG
ENST00000681589.1:n.1243+36_1243+38delinsCTG
ENST00000681784.1:n.1107+36_1107+38delinsCTG
ENST00000681886.1:c.*222+36_*222+38delinsCTG	ENSP00000506500.1:n.*222+36_*222+38delinsCTG
ENST00000308982.11:c.1029+36_1029+38delinsCTG	ENSP00000312618.7:n.1029+36_1029+38delinsCTG
ENST00000505192.5:c.*725+36_*725+38delinsCTG	ENSP00000426277.1:n.*725+36_*725+38delinsCTG
ENST00000505867.5:c.*829+36_*829+38delinsCTG	ENSP00000425346.1:n.*829+36_*829+38delinsCTG
ENST00000508971.1:c.318+36_318+38delinsCTG	ENSP00000422683.1:n.318+36_318+38delinsCTG
ENST00000511227.5:c.*923+36_*923+38delinsCTG	ENSP00000425226.1:n.*923+36_*923+38delinsCTG
ENST00000511526.5:n.534+36_534+38delinsCTG
NM_014049.4:c.1029+36_1029+38delinsCTG	NP_054768.2:n.1029+36_1029+38delinsCTG
NR_033426.1:n.1407+36_1407+38delinsCTG
XM_011512742.1:c.660+36_660+38delinsCTG	XP_011511044.1:n.660+36_660+38delinsCTG
XR_427367.1:n.1105+36_1105+38delinsCTG
XM_024453484.1:c.660+36_660+38delinsCTG	XP_024309252.1:n.660+36_660+38delinsCTG
XM_024453485.1:c.660+36_660+38delinsCTG	XP_024309253.1:n.660+36_660+38delinsCTG
XR_427367.3:n.1105+36_1105+38delinsCTG
NM_014049.5:c.1029+36_1029+38delinsCTG MANE Select	NP_054768.2:n.1029+36_1029+38delinsCTG
NR_033426.2:n.1277+36_1277+38delinsCTG