Canonical Allele Identifier: CA1400924428

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904272_128904276delinsGGCTT , CM000665.2:g.128904272_128904276delinsGGCTT	GRCh38
NC_000003.11:g.128623115_128623119delinsGGCTT , CM000665.1:g.128623115_128623119delinsGGCTT	GRCh37
NC_000003.10:g.130105805_130105809delinsGGCTT	NCBI36
NG_017064.1:g.29783_29787delinsGGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1030-114_1030-110delinsGGCTT MANE Select	ENSP00000312618.7:n.1030-114_1030-110delinsGGCTT
ENST00000511325.2:n.1108-114_1108-110delinsGGCTT
ENST00000679399.1:c.*924-114_*924-110delinsGGCTT	ENSP00000505434.1:n.*924-114_*924-110delinsGGCTT
ENST00000679431.1:c.*906-114_*906-110delinsGGCTT	ENSP00000506440.1:n.*906-114_*906-110delinsGGCTT
ENST00000679613.1:c.1030-114_1030-110delinsGGCTT	ENSP00000504971.1:n.1030-114_1030-110delinsGGCTT
ENST00000679715.1:c.661-114_661-110delinsGGCTT	ENSP00000506228.1:n.661-114_661-110delinsGGCTT
ENST00000679824.1:c.*2336-114_*2336-110delinsGGCTT	ENSP00000505516.1:n.*2336-114_*2336-110delinsGGCTT
ENST00000679990.1:n.1265-114_1265-110delinsGGCTT
ENST00000680636.1:c.1030-114_1030-110delinsGGCTT	ENSP00000504886.1:n.1030-114_1030-110delinsGGCTT
ENST00000680744.1:c.*383-114_*383-110delinsGGCTT	ENSP00000505243.1:n.*383-114_*383-110delinsGGCTT
ENST00000680764.1:c.*2434-114_*2434-110delinsGGCTT	ENSP00000505126.1:n.*2434-114_*2434-110delinsGGCTT
ENST00000681319.1:n.1108-114_1108-110delinsGGCTT
ENST00000681367.1:c.1030-114_1030-110delinsGGCTT	ENSP00000505309.1:n.1030-114_1030-110delinsGGCTT
ENST00000681552.1:c.1030-114_1030-110delinsGGCTT	ENSP00000505699.1:n.1030-114_1030-110delinsGGCTT
ENST00000681583.1:c.1030-114_1030-110delinsGGCTT	ENSP00000506340.1:n.1030-114_1030-110delinsGGCTT
ENST00000681585.1:c.1030-114_1030-110delinsGGCTT	ENSP00000506316.1:n.1030-114_1030-110delinsGGCTT
ENST00000681589.1:n.1244-114_1244-110delinsGGCTT
ENST00000681784.1:n.1108-114_1108-110delinsGGCTT
ENST00000681886.1:c.*223-114_*223-110delinsGGCTT	ENSP00000506500.1:n.*223-114_*223-110delinsGGCTT
ENST00000308982.11:c.1030-114_1030-110delinsGGCTT	ENSP00000312618.7:n.1030-114_1030-110delinsGGCTT
ENST00000505192.5:c.*726-114_*726-110delinsGGCTT	ENSP00000426277.1:n.*726-114_*726-110delinsGGCTT
ENST00000505867.5:c.*830-114_*830-110delinsGGCTT	ENSP00000425346.1:n.*830-114_*830-110delinsGGCTT
ENST00000508971.1:c.319-114_319-110delinsGGCTT	ENSP00000422683.1:n.319-114_319-110delinsGGCTT
ENST00000511227.5:c.*924-114_*924-110delinsGGCTT	ENSP00000425226.1:n.*924-114_*924-110delinsGGCTT
ENST00000511526.5:n.535-86_535-82delinsGGCTT
NM_014049.4:c.1030-114_1030-110delinsGGCTT	NP_054768.2:n.1030-114_1030-110delinsGGCTT
NR_033426.1:n.1408-114_1408-110delinsGGCTT
XM_011512742.1:c.661-114_661-110delinsGGCTT	XP_011511044.1:n.661-114_661-110delinsGGCTT
XR_427367.1:n.1106-114_1106-110delinsGGCTT
XM_024453484.1:c.661-114_661-110delinsGGCTT	XP_024309252.1:n.661-114_661-110delinsGGCTT
XM_024453485.1:c.661-114_661-110delinsGGCTT	XP_024309253.1:n.661-114_661-110delinsGGCTT
XR_427367.3:n.1106-114_1106-110delinsGGCTT
NM_014049.5:c.1030-114_1030-110delinsGGCTT MANE Select	NP_054768.2:n.1030-114_1030-110delinsGGCTT
NR_033426.2:n.1278-114_1278-110delinsGGCTT