Canonical Allele Identifier: CA2667561344

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909346-CAGTGCCAACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909350_128909359del , CM000665.2:g.128909350_128909359del	GRCh38
NC_000003.11:g.128628193_128628202del , CM000665.1:g.128628193_128628202del	GRCh37
NC_000003.10:g.130110883_130110892del	NCBI36
NG_017064.1:g.34861_34870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1492_1501del MANE Select	ENSP00000312618.7:p.Ala498LeufsTer30
ENST00000511325.2:n.1570_1579del
ENST00000679399.1:c.*1663_*1672del	ENSP00000505434.1:n.*1663_*1672del
ENST00000679431.1:c.*1368_*1377del	ENSP00000506440.1:n.*1368_*1377del
ENST00000679613.1:c.1492_1501del	ENSP00000504971.1:p.Ala498LeufsTer30
ENST00000679715.1:c.1123_1132del	ENSP00000506228.1:p.Ala375LeufsTer30
ENST00000679824.1:c.*2798_*2807del	ENSP00000505516.1:n.*2798_*2807del
ENST00000679990.1:n.1727_1736del
ENST00000680636.1:c.1492_1501del	ENSP00000504886.1:p.Ala498LeufsTer?
ENST00000680638.1:n.1245_1254del
ENST00000680744.1:c.*845_*854del	ENSP00000505243.1:n.*845_*854del
ENST00000680764.1:c.*2896_*2905del	ENSP00000505126.1:n.*2896_*2905del
ENST00000681319.1:n.2278_2287del
ENST00000681367.1:c.1492_1501del	ENSP00000505309.1:p.Ala498LeufsTer30
ENST00000681552.1:c.1150-3157_1150-3148del	ENSP00000505699.1:n.1150-3157_1150-3148del
ENST00000681583.1:c.1492_1501del	ENSP00000506340.1:p.Ala498LeufsTer30
ENST00000681585.1:c.*111_*120del	ENSP00000506316.1:n.*111_*120del
ENST00000681784.1:n.1570_1579del
ENST00000681886.1:c.*685_*694del	ENSP00000506500.1:n.*685_*694del
ENST00000308982.11:c.1492_1501del	ENSP00000312618.7:p.Ala498LeufsTer30
ENST00000505867.5:c.*1292_*1301del	ENSP00000425346.1:n.*1292_*1301del
ENST00000508971.1:c.781_790del	ENSP00000422683.1:p.Ala261LeufsTer30
ENST00000511227.5:c.*1386_*1395del	ENSP00000425226.1:n.*1386_*1395del
ENST00000511325.1:n.473_482del
ENST00000511526.5:n.1025_1034del
NM_014049.4:c.1492_1501del	NP_054768.2:p.Ala498LeufsTer30
NR_033426.1:n.1870_1879del
XM_011512742.1:c.1123_1132del	XP_011511044.1:p.Ala375LeufsTer30
XM_024453484.1:c.1123_1132del	XP_024309252.1:p.Ala375LeufsTer30
XM_024453485.1:c.1123_1132del	XP_024309253.1:p.Ala375LeufsTer30
XR_427367.3:n.1568_1577del
NM_014049.5:c.1492_1501del MANE Select	NP_054768.2:p.Ala498LeufsTer30
NR_033426.2:n.1740_1749del