Canonical Allele Identifier: CA898718304

Gene: ACAD9

Linked Data

• dbSNP Id: rs1170942692
• MyVariant Identifiers: chr3:g.128621154_128621155insTACA (hg19) ; chr3:g.128902311_128902312insTACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902312_128902315dup , CM000665.2:g.128902312_128902315dup	GRCh38
NC_000003.11:g.128621155_128621158dup , CM000665.1:g.128621155_128621158dup	GRCh37
NC_000003.10:g.130103845_130103848dup	NCBI36
NG_017064.1:g.27823_27826dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.883-241_883-238dup MANE Select	ENSP00000312618.7:n.883-241_883-238dup
ENST00000511325.2:n.961-241_961-238dup
ENST00000679399.1:c.*777-241_*777-238dup	ENSP00000505434.1:n.*777-241_*777-238dup
ENST00000679431.1:c.*755-241_*755-238dup	ENSP00000506440.1:n.*755-241_*755-238dup
ENST00000679613.1:c.883-241_883-238dup	ENSP00000504971.1:n.883-241_883-238dup
ENST00000679715.1:c.514-241_514-238dup	ENSP00000506228.1:n.514-241_514-238dup
ENST00000679824.1:c.*2189-241_*2189-238dup	ENSP00000505516.1:n.*2189-241_*2189-238dup
ENST00000679990.1:n.1118-241_1118-238dup
ENST00000680636.1:c.883-241_883-238dup	ENSP00000504886.1:n.883-241_883-238dup
ENST00000680744.1:c.*236-241_*236-238dup	ENSP00000505243.1:n.*236-241_*236-238dup
ENST00000680764.1:c.*2283-241_*2283-238dup	ENSP00000505126.1:n.*2283-241_*2283-238dup
ENST00000681319.1:n.961-241_961-238dup
ENST00000681367.1:c.883-241_883-238dup	ENSP00000505309.1:n.883-241_883-238dup
ENST00000681552.1:c.883-241_883-238dup	ENSP00000505699.1:n.883-241_883-238dup
ENST00000681583.1:c.883-241_883-238dup	ENSP00000506340.1:n.883-241_883-238dup
ENST00000681585.1:c.883-241_883-238dup	ENSP00000506316.1:n.883-241_883-238dup
ENST00000681589.1:n.1097-241_1097-238dup
ENST00000681784.1:n.961-241_961-238dup
ENST00000681886.1:c.*76-241_*76-238dup	ENSP00000506500.1:n.*76-241_*76-238dup
ENST00000308982.11:c.883-241_883-238dup	ENSP00000312618.7:n.883-241_883-238dup
ENST00000505192.5:c.*579-241_*579-238dup	ENSP00000426277.1:n.*579-241_*579-238dup
ENST00000505867.5:c.*683-241_*683-238dup	ENSP00000425346.1:n.*683-241_*683-238dup
ENST00000508971.1:c.172-241_172-238dup	ENSP00000422683.1:n.172-241_172-238dup
ENST00000511227.5:c.*777-241_*777-238dup	ENSP00000425226.1:n.*777-241_*777-238dup
ENST00000511526.5:n.384-241_384-238dup
NM_014049.4:c.883-241_883-238dup	NP_054768.2:n.883-241_883-238dup
NR_033426.1:n.1261-241_1261-238dup
XM_011512742.1:c.514-241_514-238dup	XP_011511044.1:n.514-241_514-238dup
XR_427367.1:n.955-241_955-238dup
XM_024453484.1:c.514-241_514-238dup	XP_024309252.1:n.514-241_514-238dup
XM_024453485.1:c.514-241_514-238dup	XP_024309253.1:n.514-241_514-238dup
XR_427367.3:n.955-241_955-238dup
NM_014049.5:c.883-241_883-238dup MANE Select	NP_054768.2:n.883-241_883-238dup
NR_033426.2:n.1131-241_1131-238dup