Canonical Allele Identifier: CA898718639

Gene: ACAD9

Linked Data

• dbSNP Id: rs1366989397
• gnomAD v3: 3-128902816-T-TTCCGCATTCC
• gnomAD v4: 3-128902816-T-TTCCGCATTCC
• MyVariant Identifiers: chr3:g.128621659_128621660insTCCGCATTCC (hg19) ; chr3:g.128902816_128902817insTCCGCATTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902819_128902828dup , CM000665.2:g.128902819_128902828dup	GRCh38
NC_000003.11:g.128621662_128621671dup , CM000665.1:g.128621662_128621671dup	GRCh37
NC_000003.10:g.130104352_130104361dup	NCBI36
NG_017064.1:g.28330_28339dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+191_958+200dup MANE Select	ENSP00000312618.7:n.958+191_958+200dup
ENST00000511325.2:n.1036+191_1036+200dup
ENST00000679399.1:c.*852+191_*852+200dup	ENSP00000505434.1:n.*852+191_*852+200dup
ENST00000679431.1:c.*834+187_*834+196dup	ENSP00000506440.1:n.*834+187_*834+196dup
ENST00000679613.1:c.958+191_958+200dup	ENSP00000504971.1:n.958+191_958+200dup
ENST00000679715.1:c.589+191_589+200dup	ENSP00000506228.1:n.589+191_589+200dup
ENST00000679824.1:c.*2264+191_*2264+200dup	ENSP00000505516.1:n.*2264+191_*2264+200dup
ENST00000679990.1:n.1193+191_1193+200dup
ENST00000680636.1:c.958+191_958+200dup	ENSP00000504886.1:n.958+191_958+200dup
ENST00000680744.1:c.*311+191_*311+200dup	ENSP00000505243.1:n.*311+191_*311+200dup
ENST00000680764.1:c.*2362+187_*2362+196dup	ENSP00000505126.1:n.*2362+187_*2362+196dup
ENST00000681319.1:n.1036+191_1036+200dup
ENST00000681367.1:c.958+191_958+200dup	ENSP00000505309.1:n.958+191_958+200dup
ENST00000681552.1:c.958+191_958+200dup	ENSP00000505699.1:n.958+191_958+200dup
ENST00000681583.1:c.958+191_958+200dup	ENSP00000506340.1:n.958+191_958+200dup
ENST00000681585.1:c.958+191_958+200dup	ENSP00000506316.1:n.958+191_958+200dup
ENST00000681589.1:n.1172+191_1172+200dup
ENST00000681784.1:n.1036+191_1036+200dup
ENST00000681886.1:c.*151+191_*151+200dup	ENSP00000506500.1:n.*151+191_*151+200dup
ENST00000308982.11:c.958+191_958+200dup	ENSP00000312618.7:n.958+191_958+200dup
ENST00000505192.5:c.*654+191_*654+200dup	ENSP00000426277.1:n.*654+191_*654+200dup
ENST00000505867.5:c.*758+191_*758+200dup	ENSP00000425346.1:n.*758+191_*758+200dup
ENST00000508971.1:c.247+191_247+200dup	ENSP00000422683.1:n.247+191_247+200dup
ENST00000511227.5:c.*852+191_*852+200dup	ENSP00000425226.1:n.*852+191_*852+200dup
ENST00000511526.5:n.463+187_463+196dup
NM_014049.4:c.958+191_958+200dup	NP_054768.2:n.958+191_958+200dup
NR_033426.1:n.1336+191_1336+200dup
XM_011512742.1:c.589+191_589+200dup	XP_011511044.1:n.589+191_589+200dup
XR_427367.1:n.1034+187_1034+196dup
XM_024453484.1:c.589+191_589+200dup	XP_024309252.1:n.589+191_589+200dup
XM_024453485.1:c.589+191_589+200dup	XP_024309253.1:n.589+191_589+200dup
XR_427367.3:n.1034+187_1034+196dup
NM_014049.5:c.958+191_958+200dup MANE Select	NP_054768.2:n.958+191_958+200dup
NR_033426.2:n.1206+191_1206+200dup