Canonical Allele Identifier: CA2667560120

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128902778-CAGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902779_128902782del , CM000665.2:g.128902779_128902782del	GRCh38
NC_000003.11:g.128621622_128621625del , CM000665.1:g.128621622_128621625del	GRCh37
NC_000003.10:g.130104312_130104315del	NCBI36
NG_017064.1:g.28290_28293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+151_958+154del MANE Select	ENSP00000312618.7:n.958+151_958+154del
ENST00000511325.2:n.1036+151_1036+154del
ENST00000679399.1:c.*852+151_*852+154del	ENSP00000505434.1:n.*852+151_*852+154del
ENST00000679431.1:c.*834+147_*834+150del	ENSP00000506440.1:n.*834+147_*834+150del
ENST00000679613.1:c.958+151_958+154del	ENSP00000504971.1:n.958+151_958+154del
ENST00000679715.1:c.589+151_589+154del	ENSP00000506228.1:n.589+151_589+154del
ENST00000679824.1:c.*2264+151_*2264+154del	ENSP00000505516.1:n.*2264+151_*2264+154del
ENST00000679990.1:n.1193+151_1193+154del
ENST00000680636.1:c.958+151_958+154del	ENSP00000504886.1:n.958+151_958+154del
ENST00000680744.1:c.*311+151_*311+154del	ENSP00000505243.1:n.*311+151_*311+154del
ENST00000680764.1:c.*2362+147_*2362+150del	ENSP00000505126.1:n.*2362+147_*2362+150del
ENST00000681319.1:n.1036+151_1036+154del
ENST00000681367.1:c.958+151_958+154del	ENSP00000505309.1:n.958+151_958+154del
ENST00000681552.1:c.958+151_958+154del	ENSP00000505699.1:n.958+151_958+154del
ENST00000681583.1:c.958+151_958+154del	ENSP00000506340.1:n.958+151_958+154del
ENST00000681585.1:c.958+151_958+154del	ENSP00000506316.1:n.958+151_958+154del
ENST00000681589.1:n.1172+151_1172+154del
ENST00000681784.1:n.1036+151_1036+154del
ENST00000681886.1:c.*151+151_*151+154del	ENSP00000506500.1:n.*151+151_*151+154del
ENST00000308982.11:c.958+151_958+154del	ENSP00000312618.7:n.958+151_958+154del
ENST00000505192.5:c.*654+151_*654+154del	ENSP00000426277.1:n.*654+151_*654+154del
ENST00000505867.5:c.*758+151_*758+154del	ENSP00000425346.1:n.*758+151_*758+154del
ENST00000508971.1:c.247+151_247+154del	ENSP00000422683.1:n.247+151_247+154del
ENST00000511227.5:c.*852+151_*852+154del	ENSP00000425226.1:n.*852+151_*852+154del
ENST00000511526.5:n.463+147_463+150del
NM_014049.4:c.958+151_958+154del	NP_054768.2:n.958+151_958+154del
NR_033426.1:n.1336+151_1336+154del
XM_011512742.1:c.589+151_589+154del	XP_011511044.1:n.589+151_589+154del
XR_427367.1:n.1034+147_1034+150del
XM_024453484.1:c.589+151_589+154del	XP_024309252.1:n.589+151_589+154del
XM_024453485.1:c.589+151_589+154del	XP_024309253.1:n.589+151_589+154del
XR_427367.3:n.1034+147_1034+150del
NM_014049.5:c.958+151_958+154del MANE Select	NP_054768.2:n.958+151_958+154del
NR_033426.2:n.1206+151_1206+154del