Canonical Allele Identifier: CA1400923791

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902877_128902882delinsCTGGGG , CM000665.2:g.128902877_128902882delinsCTGGGG	GRCh38
NC_000003.11:g.128621720_128621725delinsCTGGGG , CM000665.1:g.128621720_128621725delinsCTGGGG	GRCh37
NC_000003.10:g.130104410_130104415delinsCTGGGG	NCBI36
NG_017064.1:g.28388_28393delinsCTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+249_958+254delinsCTGGGG MANE Select	ENSP00000312618.7:n.958+249_958+254delinsCTGGGG
ENST00000511325.2:n.1036+249_1036+254delinsCTGGGG
ENST00000679399.1:c.*852+249_*852+254delinsCTGGGG	ENSP00000505434.1:n.*852+249_*852+254delinsCTGGGG
ENST00000679431.1:c.*834+245_*834+250delinsCTGGGG	ENSP00000506440.1:n.*834+245_*834+250delinsCTGGGG
ENST00000679613.1:c.958+249_958+254delinsCTGGGG	ENSP00000504971.1:n.958+249_958+254delinsCTGGGG
ENST00000679715.1:c.589+249_589+254delinsCTGGGG	ENSP00000506228.1:n.589+249_589+254delinsCTGGGG
ENST00000679824.1:c.*2264+249_*2264+254delinsCTGGGG	ENSP00000505516.1:n.*2264+249_*2264+254delinsCTGGGG
ENST00000679990.1:n.1193+249_1193+254delinsCTGGGG
ENST00000680636.1:c.958+249_958+254delinsCTGGGG	ENSP00000504886.1:n.958+249_958+254delinsCTGGGG
ENST00000680744.1:c.*311+249_*311+254delinsCTGGGG	ENSP00000505243.1:n.*311+249_*311+254delinsCTGGGG
ENST00000680764.1:c.*2362+245_*2362+250delinsCTGGGG	ENSP00000505126.1:n.*2362+245_*2362+250delinsCTGGGG
ENST00000681319.1:n.1036+249_1036+254delinsCTGGGG
ENST00000681367.1:c.958+249_958+254delinsCTGGGG	ENSP00000505309.1:n.958+249_958+254delinsCTGGGG
ENST00000681552.1:c.958+249_958+254delinsCTGGGG	ENSP00000505699.1:n.958+249_958+254delinsCTGGGG
ENST00000681583.1:c.958+249_958+254delinsCTGGGG	ENSP00000506340.1:n.958+249_958+254delinsCTGGGG
ENST00000681585.1:c.958+249_958+254delinsCTGGGG	ENSP00000506316.1:n.958+249_958+254delinsCTGGGG
ENST00000681589.1:n.1172+249_1172+254delinsCTGGGG
ENST00000681784.1:n.1036+249_1036+254delinsCTGGGG
ENST00000681886.1:c.*151+249_*151+254delinsCTGGGG	ENSP00000506500.1:n.*151+249_*151+254delinsCTGGGG
ENST00000308982.11:c.958+249_958+254delinsCTGGGG	ENSP00000312618.7:n.958+249_958+254delinsCTGGGG
ENST00000505192.5:c.*654+249_*654+254delinsCTGGGG	ENSP00000426277.1:n.*654+249_*654+254delinsCTGGGG
ENST00000505867.5:c.*758+249_*758+254delinsCTGGGG	ENSP00000425346.1:n.*758+249_*758+254delinsCTGGGG
ENST00000508971.1:c.247+249_247+254delinsCTGGGG	ENSP00000422683.1:n.247+249_247+254delinsCTGGGG
ENST00000511227.5:c.*852+249_*852+254delinsCTGGGG	ENSP00000425226.1:n.*852+249_*852+254delinsCTGGGG
ENST00000511526.5:n.463+245_463+250delinsCTGGGG
NM_014049.4:c.958+249_958+254delinsCTGGGG	NP_054768.2:n.958+249_958+254delinsCTGGGG
NR_033426.1:n.1336+249_1336+254delinsCTGGGG
XM_011512742.1:c.589+249_589+254delinsCTGGGG	XP_011511044.1:n.589+249_589+254delinsCTGGGG
XR_427367.1:n.1034+245_1034+250delinsCTGGGG
XM_024453484.1:c.589+249_589+254delinsCTGGGG	XP_024309252.1:n.589+249_589+254delinsCTGGGG
XM_024453485.1:c.589+249_589+254delinsCTGGGG	XP_024309253.1:n.589+249_589+254delinsCTGGGG
XR_427367.3:n.1034+245_1034+250delinsCTGGGG
NM_014049.5:c.958+249_958+254delinsCTGGGG MANE Select	NP_054768.2:n.958+249_958+254delinsCTGGGG
NR_033426.2:n.1206+249_1206+254delinsCTGGGG