Canonical Allele Identifier: CA1400923765

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902825_128902827delinsCCT , CM000665.2:g.128902825_128902827delinsCCT	GRCh38
NC_000003.11:g.128621668_128621670delinsCCT , CM000665.1:g.128621668_128621670delinsCCT	GRCh37
NC_000003.10:g.130104358_130104360delinsCCT	NCBI36
NG_017064.1:g.28336_28338delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+197_958+199delinsCCT MANE Select	ENSP00000312618.7:n.958+197_958+199delinsCCT
ENST00000511325.2:n.1036+197_1036+199delinsCCT
ENST00000679399.1:c.*852+197_*852+199delinsCCT	ENSP00000505434.1:n.*852+197_*852+199delinsCCT
ENST00000679431.1:c.*834+193_*834+195delinsCCT	ENSP00000506440.1:n.*834+193_*834+195delinsCCT
ENST00000679613.1:c.958+197_958+199delinsCCT	ENSP00000504971.1:n.958+197_958+199delinsCCT
ENST00000679715.1:c.589+197_589+199delinsCCT	ENSP00000506228.1:n.589+197_589+199delinsCCT
ENST00000679824.1:c.*2264+197_*2264+199delinsCCT	ENSP00000505516.1:n.*2264+197_*2264+199delinsCCT
ENST00000679990.1:n.1193+197_1193+199delinsCCT
ENST00000680636.1:c.958+197_958+199delinsCCT	ENSP00000504886.1:n.958+197_958+199delinsCCT
ENST00000680744.1:c.*311+197_*311+199delinsCCT	ENSP00000505243.1:n.*311+197_*311+199delinsCCT
ENST00000680764.1:c.*2362+193_*2362+195delinsCCT	ENSP00000505126.1:n.*2362+193_*2362+195delinsCCT
ENST00000681319.1:n.1036+197_1036+199delinsCCT
ENST00000681367.1:c.958+197_958+199delinsCCT	ENSP00000505309.1:n.958+197_958+199delinsCCT
ENST00000681552.1:c.958+197_958+199delinsCCT	ENSP00000505699.1:n.958+197_958+199delinsCCT
ENST00000681583.1:c.958+197_958+199delinsCCT	ENSP00000506340.1:n.958+197_958+199delinsCCT
ENST00000681585.1:c.958+197_958+199delinsCCT	ENSP00000506316.1:n.958+197_958+199delinsCCT
ENST00000681589.1:n.1172+197_1172+199delinsCCT
ENST00000681784.1:n.1036+197_1036+199delinsCCT
ENST00000681886.1:c.*151+197_*151+199delinsCCT	ENSP00000506500.1:n.*151+197_*151+199delinsCCT
ENST00000308982.11:c.958+197_958+199delinsCCT	ENSP00000312618.7:n.958+197_958+199delinsCCT
ENST00000505192.5:c.*654+197_*654+199delinsCCT	ENSP00000426277.1:n.*654+197_*654+199delinsCCT
ENST00000505867.5:c.*758+197_*758+199delinsCCT	ENSP00000425346.1:n.*758+197_*758+199delinsCCT
ENST00000508971.1:c.247+197_247+199delinsCCT	ENSP00000422683.1:n.247+197_247+199delinsCCT
ENST00000511227.5:c.*852+197_*852+199delinsCCT	ENSP00000425226.1:n.*852+197_*852+199delinsCCT
ENST00000511526.5:n.463+193_463+195delinsCCT
NM_014049.4:c.958+197_958+199delinsCCT	NP_054768.2:n.958+197_958+199delinsCCT
NR_033426.1:n.1336+197_1336+199delinsCCT
XM_011512742.1:c.589+197_589+199delinsCCT	XP_011511044.1:n.589+197_589+199delinsCCT
XR_427367.1:n.1034+193_1034+195delinsCCT
XM_024453484.1:c.589+197_589+199delinsCCT	XP_024309252.1:n.589+197_589+199delinsCCT
XM_024453485.1:c.589+197_589+199delinsCCT	XP_024309253.1:n.589+197_589+199delinsCCT
XR_427367.3:n.1034+193_1034+195delinsCCT
NM_014049.5:c.958+197_958+199delinsCCT MANE Select	NP_054768.2:n.958+197_958+199delinsCCT
NR_033426.2:n.1206+197_1206+199delinsCCT