Canonical Allele Identifier: CA435591760

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128904090-G-A
• MyVariant Identifiers: chr3:g.128622933G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904090G>A , CM000665.2:g.128904090G>A	GRCh38
NC_000003.11:g.128622933G>A , CM000665.1:g.128622933G>A	GRCh37
NC_000003.10:g.130105623G>A	NCBI36
NG_017064.1:g.29601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.987G>A MANE Select	ENSP00000312618.7:p.Arg329=
ENST00000511325.2:n.1065G>A
ENST00000679399.1:c.*881G>A	ENSP00000505434.1:n.*881G>A
ENST00000679431.1:c.*863G>A	ENSP00000506440.1:n.*863G>A
ENST00000679613.1:c.987G>A	ENSP00000504971.1:p.Arg329=
ENST00000679715.1:c.618G>A	ENSP00000506228.1:p.Arg206=
ENST00000679824.1:c.*2293G>A	ENSP00000505516.1:n.*2293G>A
ENST00000679990.1:n.1222G>A
ENST00000680636.1:c.987G>A	ENSP00000504886.1:p.Arg329=
ENST00000680744.1:c.*340G>A	ENSP00000505243.1:n.*340G>A
ENST00000680764.1:c.*2391G>A	ENSP00000505126.1:n.*2391G>A
ENST00000681319.1:n.1065G>A
ENST00000681367.1:c.987G>A	ENSP00000505309.1:p.Arg329=
ENST00000681552.1:c.987G>A	ENSP00000505699.1:p.Arg329=
ENST00000681583.1:c.987G>A	ENSP00000506340.1:p.Arg329=
ENST00000681585.1:c.987G>A	ENSP00000506316.1:p.Arg329=
ENST00000681589.1:n.1201G>A
ENST00000681784.1:n.1065G>A
ENST00000681886.1:c.*180G>A	ENSP00000506500.1:n.*180G>A
ENST00000308982.11:c.987G>A	ENSP00000312618.7:p.Arg329=
ENST00000505192.5:c.*683G>A	ENSP00000426277.1:n.*683G>A
ENST00000505867.5:c.*787G>A	ENSP00000425346.1:n.*787G>A
ENST00000508971.1:c.276G>A	ENSP00000422683.1:p.Arg92=
ENST00000511227.5:c.*881G>A	ENSP00000425226.1:n.*881G>A
ENST00000511526.5:n.492G>A
NM_014049.4:c.987G>A	NP_054768.2:p.Arg329=
NR_033426.1:n.1365G>A
XM_011512742.1:c.618G>A	XP_011511044.1:p.Arg206=
XR_427367.1:n.1063G>A
XM_024453484.1:c.618G>A	XP_024309252.1:p.Arg206=
XM_024453485.1:c.618G>A	XP_024309253.1:p.Arg206=
XR_427367.3:n.1063G>A
NM_014049.5:c.987G>A MANE Select	NP_054768.2:p.Arg329=
NR_033426.2:n.1235G>A