Canonical Allele Identifier: CA898718670

Gene: ACAD9

Linked Data

• dbSNP Id: rs1286883798
• gnomAD v3: 3-128902877-CTGGGG-C
• gnomAD v4: 3-128902877-CTGGGG-C
• MyVariant Identifiers: chr3:g.128621721_128621725del (hg19) ; chr3:g.128902878_128902882del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902883_128902887del , CM000665.2:g.128902883_128902887del	GRCh38
NC_000003.11:g.128621726_128621730del , CM000665.1:g.128621726_128621730del	GRCh37
NC_000003.10:g.130104416_130104420del	NCBI36
NG_017064.1:g.28394_28398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+255_958+259del MANE Select	ENSP00000312618.7:n.958+255_958+259del
ENST00000511325.2:n.1036+255_1036+259del
ENST00000679399.1:c.*852+255_*852+259del	ENSP00000505434.1:n.*852+255_*852+259del
ENST00000679431.1:c.*834+251_*834+255del	ENSP00000506440.1:n.*834+251_*834+255del
ENST00000679613.1:c.958+255_958+259del	ENSP00000504971.1:n.958+255_958+259del
ENST00000679715.1:c.589+255_589+259del	ENSP00000506228.1:n.589+255_589+259del
ENST00000679824.1:c.*2264+255_*2264+259del	ENSP00000505516.1:n.*2264+255_*2264+259del
ENST00000679990.1:n.1193+255_1193+259del
ENST00000680636.1:c.958+255_958+259del	ENSP00000504886.1:n.958+255_958+259del
ENST00000680744.1:c.*311+255_*311+259del	ENSP00000505243.1:n.*311+255_*311+259del
ENST00000680764.1:c.*2362+251_*2362+255del	ENSP00000505126.1:n.*2362+251_*2362+255del
ENST00000681319.1:n.1036+255_1036+259del
ENST00000681367.1:c.958+255_958+259del	ENSP00000505309.1:n.958+255_958+259del
ENST00000681552.1:c.958+255_958+259del	ENSP00000505699.1:n.958+255_958+259del
ENST00000681583.1:c.958+255_958+259del	ENSP00000506340.1:n.958+255_958+259del
ENST00000681585.1:c.958+255_958+259del	ENSP00000506316.1:n.958+255_958+259del
ENST00000681589.1:n.1172+255_1172+259del
ENST00000681784.1:n.1036+255_1036+259del
ENST00000681886.1:c.*151+255_*151+259del	ENSP00000506500.1:n.*151+255_*151+259del
ENST00000308982.11:c.958+255_958+259del	ENSP00000312618.7:n.958+255_958+259del
ENST00000505192.5:c.*654+255_*654+259del	ENSP00000426277.1:n.*654+255_*654+259del
ENST00000505867.5:c.*758+255_*758+259del	ENSP00000425346.1:n.*758+255_*758+259del
ENST00000508971.1:c.247+255_247+259del	ENSP00000422683.1:n.247+255_247+259del
ENST00000511227.5:c.*852+255_*852+259del	ENSP00000425226.1:n.*852+255_*852+259del
ENST00000511526.5:n.463+251_463+255del
NM_014049.4:c.958+255_958+259del	NP_054768.2:n.958+255_958+259del
NR_033426.1:n.1336+255_1336+259del
XM_011512742.1:c.589+255_589+259del	XP_011511044.1:n.589+255_589+259del
XR_427367.1:n.1034+251_1034+255del
XM_024453484.1:c.589+255_589+259del	XP_024309252.1:n.589+255_589+259del
XM_024453485.1:c.589+255_589+259del	XP_024309253.1:n.589+255_589+259del
XR_427367.3:n.1034+251_1034+255del
NM_014049.5:c.958+255_958+259del MANE Select	NP_054768.2:n.958+255_958+259del
NR_033426.2:n.1206+255_1206+259del