Canonical Allele Identifier: CA435591757

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128622930A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904087A>T , CM000665.2:g.128904087A>T	GRCh38
NC_000003.11:g.128622930A>T , CM000665.1:g.128622930A>T	GRCh37
NC_000003.10:g.130105620A>T	NCBI36
NG_017064.1:g.29598A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.984A>T MANE Select	ENSP00000312618.7:p.Thr328=
ENST00000511325.2:n.1062A>T
ENST00000679399.1:c.*878A>T	ENSP00000505434.1:n.*878A>T
ENST00000679431.1:c.*860A>T	ENSP00000506440.1:n.*860A>T
ENST00000679613.1:c.984A>T	ENSP00000504971.1:p.Thr328=
ENST00000679715.1:c.615A>T	ENSP00000506228.1:p.Thr205=
ENST00000679824.1:c.*2290A>T	ENSP00000505516.1:n.*2290A>T
ENST00000679990.1:n.1219A>T
ENST00000680636.1:c.984A>T	ENSP00000504886.1:p.Thr328=
ENST00000680744.1:c.*337A>T	ENSP00000505243.1:n.*337A>T
ENST00000680764.1:c.*2388A>T	ENSP00000505126.1:n.*2388A>T
ENST00000681319.1:n.1062A>T
ENST00000681367.1:c.984A>T	ENSP00000505309.1:p.Thr328=
ENST00000681552.1:c.984A>T	ENSP00000505699.1:p.Thr328=
ENST00000681583.1:c.984A>T	ENSP00000506340.1:p.Thr328=
ENST00000681585.1:c.984A>T	ENSP00000506316.1:p.Thr328=
ENST00000681589.1:n.1198A>T
ENST00000681784.1:n.1062A>T
ENST00000681886.1:c.*177A>T	ENSP00000506500.1:n.*177A>T
ENST00000308982.11:c.984A>T	ENSP00000312618.7:p.Thr328=
ENST00000505192.5:c.*680A>T	ENSP00000426277.1:n.*680A>T
ENST00000505867.5:c.*784A>T	ENSP00000425346.1:n.*784A>T
ENST00000508971.1:c.273A>T	ENSP00000422683.1:p.Thr91=
ENST00000511227.5:c.*878A>T	ENSP00000425226.1:n.*878A>T
ENST00000511526.5:n.489A>T
NM_014049.4:c.984A>T	NP_054768.2:p.Thr328=
NR_033426.1:n.1362A>T
XM_011512742.1:c.615A>T	XP_011511044.1:p.Thr205=
XR_427367.1:n.1060A>T
XM_024453484.1:c.615A>T	XP_024309252.1:p.Thr205=
XM_024453485.1:c.615A>T	XP_024309253.1:p.Thr205=
XR_427367.3:n.1060A>T
NM_014049.5:c.984A>T MANE Select	NP_054768.2:p.Thr328=
NR_033426.2:n.1232A>T