Canonical Allele Identifier: CA2758351709

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904244_128904245del , CM000665.2:g.128904244_128904245del	GRCh38
NC_000003.11:g.128623087_128623088del , CM000665.1:g.128623087_128623088del	GRCh37
NC_000003.10:g.130105777_130105778del	NCBI36
NG_017064.1:g.29755_29756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+112_1029+113del MANE Select	ENSP00000312618.7:n.1029+112_1029+113del
ENST00000511325.2:n.1107+112_1107+113del
ENST00000679399.1:c.*923+112_*923+113del	ENSP00000505434.1:n.*923+112_*923+113del
ENST00000679431.1:c.*905+112_*905+113del	ENSP00000506440.1:n.*905+112_*905+113del
ENST00000679613.1:c.1029+112_1029+113del	ENSP00000504971.1:n.1029+112_1029+113del
ENST00000679715.1:c.660+112_660+113del	ENSP00000506228.1:n.660+112_660+113del
ENST00000679824.1:c.*2335+112_*2335+113del	ENSP00000505516.1:n.*2335+112_*2335+113del
ENST00000679990.1:n.1264+112_1264+113del
ENST00000680636.1:c.1029+112_1029+113del	ENSP00000504886.1:n.1029+112_1029+113del
ENST00000680744.1:c.*382+112_*382+113del	ENSP00000505243.1:n.*382+112_*382+113del
ENST00000680764.1:c.*2433+112_*2433+113del	ENSP00000505126.1:n.*2433+112_*2433+113del
ENST00000681319.1:n.1107+112_1107+113del
ENST00000681367.1:c.1029+112_1029+113del	ENSP00000505309.1:n.1029+112_1029+113del
ENST00000681552.1:c.1029+112_1029+113del	ENSP00000505699.1:n.1029+112_1029+113del
ENST00000681583.1:c.1029+112_1029+113del	ENSP00000506340.1:n.1029+112_1029+113del
ENST00000681585.1:c.1029+112_1029+113del	ENSP00000506316.1:n.1029+112_1029+113del
ENST00000681589.1:n.1243+112_1243+113del
ENST00000681784.1:n.1107+112_1107+113del
ENST00000681886.1:c.*222+112_*222+113del	ENSP00000506500.1:n.*222+112_*222+113del
ENST00000308982.11:c.1029+112_1029+113del	ENSP00000312618.7:n.1029+112_1029+113del
ENST00000505192.5:c.*725+112_*725+113del	ENSP00000426277.1:n.*725+112_*725+113del
ENST00000505867.5:c.*829+112_*829+113del	ENSP00000425346.1:n.*829+112_*829+113del
ENST00000508971.1:c.318+112_318+113del	ENSP00000422683.1:n.318+112_318+113del
ENST00000511227.5:c.*923+112_*923+113del	ENSP00000425226.1:n.*923+112_*923+113del
ENST00000511526.5:n.534+112_535-113del
NM_014049.4:c.1029+112_1029+113del	NP_054768.2:n.1029+112_1029+113del
NR_033426.1:n.1407+112_1407+113del
XM_011512742.1:c.660+112_660+113del	XP_011511044.1:n.660+112_660+113del
XR_427367.1:n.1105+112_1105+113del
XM_024453484.1:c.660+112_660+113del	XP_024309252.1:n.660+112_660+113del
XM_024453485.1:c.660+112_660+113del	XP_024309253.1:n.660+112_660+113del
XR_427367.3:n.1105+112_1105+113del
NM_014049.5:c.1029+112_1029+113del MANE Select	NP_054768.2:n.1029+112_1029+113del
NR_033426.2:n.1277+112_1277+113del