Canonical Allele Identifier: CA1400924424

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904262_128904263delinsCG , CM000665.2:g.128904262_128904263delinsCG	GRCh38
NC_000003.11:g.128623105_128623106delinsCG , CM000665.1:g.128623105_128623106delinsCG	GRCh37
NC_000003.10:g.130105795_130105796delinsCG	NCBI36
NG_017064.1:g.29773_29774delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1030-124_1030-123delinsCG MANE Select	ENSP00000312618.7:n.1030-124_1030-123delinsCG
ENST00000511325.2:n.1108-124_1108-123delinsCG
ENST00000679399.1:c.*924-124_*924-123delinsCG	ENSP00000505434.1:n.*924-124_*924-123delinsCG
ENST00000679431.1:c.*906-124_*906-123delinsCG	ENSP00000506440.1:n.*906-124_*906-123delinsCG
ENST00000679613.1:c.1030-124_1030-123delinsCG	ENSP00000504971.1:n.1030-124_1030-123delinsCG
ENST00000679715.1:c.661-124_661-123delinsCG	ENSP00000506228.1:n.661-124_661-123delinsCG
ENST00000679824.1:c.*2336-124_*2336-123delinsCG	ENSP00000505516.1:n.*2336-124_*2336-123delinsCG
ENST00000679990.1:n.1265-124_1265-123delinsCG
ENST00000680636.1:c.1030-124_1030-123delinsCG	ENSP00000504886.1:n.1030-124_1030-123delinsCG
ENST00000680744.1:c.*383-124_*383-123delinsCG	ENSP00000505243.1:n.*383-124_*383-123delinsCG
ENST00000680764.1:c.*2434-124_*2434-123delinsCG	ENSP00000505126.1:n.*2434-124_*2434-123delinsCG
ENST00000681319.1:n.1108-124_1108-123delinsCG
ENST00000681367.1:c.1030-124_1030-123delinsCG	ENSP00000505309.1:n.1030-124_1030-123delinsCG
ENST00000681552.1:c.1030-124_1030-123delinsCG	ENSP00000505699.1:n.1030-124_1030-123delinsCG
ENST00000681583.1:c.1030-124_1030-123delinsCG	ENSP00000506340.1:n.1030-124_1030-123delinsCG
ENST00000681585.1:c.1030-124_1030-123delinsCG	ENSP00000506316.1:n.1030-124_1030-123delinsCG
ENST00000681589.1:n.1244-124_1244-123delinsCG
ENST00000681784.1:n.1108-124_1108-123delinsCG
ENST00000681886.1:c.*223-124_*223-123delinsCG	ENSP00000506500.1:n.*223-124_*223-123delinsCG
ENST00000308982.11:c.1030-124_1030-123delinsCG	ENSP00000312618.7:n.1030-124_1030-123delinsCG
ENST00000505192.5:c.*726-124_*726-123delinsCG	ENSP00000426277.1:n.*726-124_*726-123delinsCG
ENST00000505867.5:c.*830-124_*830-123delinsCG	ENSP00000425346.1:n.*830-124_*830-123delinsCG
ENST00000508971.1:c.319-124_319-123delinsCG	ENSP00000422683.1:n.319-124_319-123delinsCG
ENST00000511227.5:c.*924-124_*924-123delinsCG	ENSP00000425226.1:n.*924-124_*924-123delinsCG
ENST00000511526.5:n.535-96_535-95delinsCG
NM_014049.4:c.1030-124_1030-123delinsCG	NP_054768.2:n.1030-124_1030-123delinsCG
NR_033426.1:n.1408-124_1408-123delinsCG
XM_011512742.1:c.661-124_661-123delinsCG	XP_011511044.1:n.661-124_661-123delinsCG
XR_427367.1:n.1106-124_1106-123delinsCG
XM_024453484.1:c.661-124_661-123delinsCG	XP_024309252.1:n.661-124_661-123delinsCG
XM_024453485.1:c.661-124_661-123delinsCG	XP_024309253.1:n.661-124_661-123delinsCG
XR_427367.3:n.1106-124_1106-123delinsCG
NM_014049.5:c.1030-124_1030-123delinsCG MANE Select	NP_054768.2:n.1030-124_1030-123delinsCG
NR_033426.2:n.1278-124_1278-123delinsCG