Canonical Allele Identifier: CA1400924392

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904203_128904205delinsCTG , CM000665.2:g.128904203_128904205delinsCTG	GRCh38
NC_000003.11:g.128623046_128623048delinsCTG , CM000665.1:g.128623046_128623048delinsCTG	GRCh37
NC_000003.10:g.130105736_130105738delinsCTG	NCBI36
NG_017064.1:g.29714_29716delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+71_1029+73delinsCTG MANE Select	ENSP00000312618.7:n.1029+71_1029+73delinsCTG
ENST00000511325.2:n.1107+71_1107+73delinsCTG
ENST00000679399.1:c.*923+71_*923+73delinsCTG	ENSP00000505434.1:n.*923+71_*923+73delinsCTG
ENST00000679431.1:c.*905+71_*905+73delinsCTG	ENSP00000506440.1:n.*905+71_*905+73delinsCTG
ENST00000679613.1:c.1029+71_1029+73delinsCTG	ENSP00000504971.1:n.1029+71_1029+73delinsCTG
ENST00000679715.1:c.660+71_660+73delinsCTG	ENSP00000506228.1:n.660+71_660+73delinsCTG
ENST00000679824.1:c.*2335+71_*2335+73delinsCTG	ENSP00000505516.1:n.*2335+71_*2335+73delinsCTG
ENST00000679990.1:n.1264+71_1264+73delinsCTG
ENST00000680636.1:c.1029+71_1029+73delinsCTG	ENSP00000504886.1:n.1029+71_1029+73delinsCTG
ENST00000680744.1:c.*382+71_*382+73delinsCTG	ENSP00000505243.1:n.*382+71_*382+73delinsCTG
ENST00000680764.1:c.*2433+71_*2433+73delinsCTG	ENSP00000505126.1:n.*2433+71_*2433+73delinsCTG
ENST00000681319.1:n.1107+71_1107+73delinsCTG
ENST00000681367.1:c.1029+71_1029+73delinsCTG	ENSP00000505309.1:n.1029+71_1029+73delinsCTG
ENST00000681552.1:c.1029+71_1029+73delinsCTG	ENSP00000505699.1:n.1029+71_1029+73delinsCTG
ENST00000681583.1:c.1029+71_1029+73delinsCTG	ENSP00000506340.1:n.1029+71_1029+73delinsCTG
ENST00000681585.1:c.1029+71_1029+73delinsCTG	ENSP00000506316.1:n.1029+71_1029+73delinsCTG
ENST00000681589.1:n.1243+71_1243+73delinsCTG
ENST00000681784.1:n.1107+71_1107+73delinsCTG
ENST00000681886.1:c.*222+71_*222+73delinsCTG	ENSP00000506500.1:n.*222+71_*222+73delinsCTG
ENST00000308982.11:c.1029+71_1029+73delinsCTG	ENSP00000312618.7:n.1029+71_1029+73delinsCTG
ENST00000505192.5:c.*725+71_*725+73delinsCTG	ENSP00000426277.1:n.*725+71_*725+73delinsCTG
ENST00000505867.5:c.*829+71_*829+73delinsCTG	ENSP00000425346.1:n.*829+71_*829+73delinsCTG
ENST00000508971.1:c.318+71_318+73delinsCTG	ENSP00000422683.1:n.318+71_318+73delinsCTG
ENST00000511227.5:c.*923+71_*923+73delinsCTG	ENSP00000425226.1:n.*923+71_*923+73delinsCTG
ENST00000511526.5:n.534+71_534+73delinsCTG
NM_014049.4:c.1029+71_1029+73delinsCTG	NP_054768.2:n.1029+71_1029+73delinsCTG
NR_033426.1:n.1407+71_1407+73delinsCTG
XM_011512742.1:c.660+71_660+73delinsCTG	XP_011511044.1:n.660+71_660+73delinsCTG
XR_427367.1:n.1105+71_1105+73delinsCTG
XM_024453484.1:c.660+71_660+73delinsCTG	XP_024309252.1:n.660+71_660+73delinsCTG
XM_024453485.1:c.660+71_660+73delinsCTG	XP_024309253.1:n.660+71_660+73delinsCTG
XR_427367.3:n.1105+71_1105+73delinsCTG
NM_014049.5:c.1029+71_1029+73delinsCTG MANE Select	NP_054768.2:n.1029+71_1029+73delinsCTG
NR_033426.2:n.1277+71_1277+73delinsCTG