Canonical Allele Identifier: CA2667560251

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128904137-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904137_128904138insT , CM000665.2:g.128904137_128904138insT	GRCh38
NC_000003.11:g.128622980_128622981insT , CM000665.1:g.128622980_128622981insT	GRCh37
NC_000003.10:g.130105670_130105671insT	NCBI36
NG_017064.1:g.29648_29649insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+5_1029+6insT MANE Select	ENSP00000312618.7:n.1029+5_1029+6insT
ENST00000511325.2:n.1107+5_1107+6insT
ENST00000679399.1:c.*923+5_*923+6insT	ENSP00000505434.1:n.*923+5_*923+6insT
ENST00000679431.1:c.*905+5_*905+6insT	ENSP00000506440.1:n.*905+5_*905+6insT
ENST00000679613.1:c.1029+5_1029+6insT	ENSP00000504971.1:n.1029+5_1029+6insT
ENST00000679715.1:c.660+5_660+6insT	ENSP00000506228.1:n.660+5_660+6insT
ENST00000679824.1:c.*2335+5_*2335+6insT	ENSP00000505516.1:n.*2335+5_*2335+6insT
ENST00000679990.1:n.1264+5_1264+6insT
ENST00000680636.1:c.1029+5_1029+6insT	ENSP00000504886.1:n.1029+5_1029+6insT
ENST00000680744.1:c.*382+5_*382+6insT	ENSP00000505243.1:n.*382+5_*382+6insT
ENST00000680764.1:c.*2433+5_*2433+6insT	ENSP00000505126.1:n.*2433+5_*2433+6insT
ENST00000681319.1:n.1107+5_1107+6insT
ENST00000681367.1:c.1029+5_1029+6insT	ENSP00000505309.1:n.1029+5_1029+6insT
ENST00000681552.1:c.1029+5_1029+6insT	ENSP00000505699.1:n.1029+5_1029+6insT
ENST00000681583.1:c.1029+5_1029+6insT	ENSP00000506340.1:n.1029+5_1029+6insT
ENST00000681585.1:c.1029+5_1029+6insT	ENSP00000506316.1:n.1029+5_1029+6insT
ENST00000681589.1:n.1243+5_1243+6insT
ENST00000681784.1:n.1107+5_1107+6insT
ENST00000681886.1:c.*222+5_*222+6insT	ENSP00000506500.1:n.*222+5_*222+6insT
ENST00000308982.11:c.1029+5_1029+6insT	ENSP00000312618.7:n.1029+5_1029+6insT
ENST00000505192.5:c.*725+5_*725+6insT	ENSP00000426277.1:n.*725+5_*725+6insT
ENST00000505867.5:c.*829+5_*829+6insT	ENSP00000425346.1:n.*829+5_*829+6insT
ENST00000508971.1:c.318+5_318+6insT	ENSP00000422683.1:n.318+5_318+6insT
ENST00000511227.5:c.*923+5_*923+6insT	ENSP00000425226.1:n.*923+5_*923+6insT
ENST00000511526.5:n.534+5_534+6insT
NM_014049.4:c.1029+5_1029+6insT	NP_054768.2:n.1029+5_1029+6insT
NR_033426.1:n.1407+5_1407+6insT
XM_011512742.1:c.660+5_660+6insT	XP_011511044.1:n.660+5_660+6insT
XR_427367.1:n.1105+5_1105+6insT
XM_024453484.1:c.660+5_660+6insT	XP_024309252.1:n.660+5_660+6insT
XM_024453485.1:c.660+5_660+6insT	XP_024309253.1:n.660+5_660+6insT
XR_427367.3:n.1105+5_1105+6insT
NM_014049.5:c.1029+5_1029+6insT MANE Select	NP_054768.2:n.1029+5_1029+6insT
NR_033426.2:n.1277+5_1277+6insT