Canonical Allele Identifier: CA354435555

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128621463G>T (hg19) ; chr3:g.128902620G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902620G>T , CM000665.2:g.128902620G>T	GRCh38
NC_000003.11:g.128621463G>T , CM000665.1:g.128621463G>T	GRCh37
NC_000003.10:g.130104153G>T	NCBI36
NG_017064.1:g.28131G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.950G>T MANE Select	ENSP00000312618.7:p.Arg317Ile
ENST00000511325.2:n.1028G>T
ENST00000679399.1:c.*844G>T	ENSP00000505434.1:n.*844G>T
ENST00000679431.1:c.*822G>T	ENSP00000506440.1:n.*822G>T
ENST00000679613.1:c.950G>T	ENSP00000504971.1:p.Arg317Ile
ENST00000679715.1:c.581G>T	ENSP00000506228.1:p.Arg194Ile
ENST00000679824.1:c.*2256G>T	ENSP00000505516.1:n.*2256G>T
ENST00000679990.1:n.1185G>T
ENST00000680636.1:c.950G>T	ENSP00000504886.1:p.Arg317Ile
ENST00000680744.1:c.*303G>T	ENSP00000505243.1:n.*303G>T
ENST00000680764.1:c.*2350G>T	ENSP00000505126.1:n.*2350G>T
ENST00000681319.1:n.1028G>T
ENST00000681367.1:c.950G>T	ENSP00000505309.1:p.Arg317Ile
ENST00000681552.1:c.950G>T	ENSP00000505699.1:p.Arg317Ile
ENST00000681583.1:c.950G>T	ENSP00000506340.1:p.Arg317Ile
ENST00000681585.1:c.950G>T	ENSP00000506316.1:p.Arg317Ile
ENST00000681589.1:n.1164G>T
ENST00000681784.1:n.1028G>T
ENST00000681886.1:c.*143G>T	ENSP00000506500.1:n.*143G>T
ENST00000308982.11:c.950G>T	ENSP00000312618.7:p.Arg317Ile
ENST00000505192.5:c.*646G>T	ENSP00000426277.1:n.*646G>T
ENST00000505867.5:c.*750G>T	ENSP00000425346.1:n.*750G>T
ENST00000508971.1:c.239G>T	ENSP00000422683.1:p.Arg80Ile
ENST00000511227.5:c.*844G>T	ENSP00000425226.1:n.*844G>T
ENST00000511526.5:n.451G>T
NM_014049.4:c.950G>T	NP_054768.2:p.Arg317Ile
NR_033426.1:n.1328G>T
XM_011512742.1:c.581G>T	XP_011511044.1:p.Arg194Ile
XR_427367.1:n.1022G>T
XM_024453484.1:c.581G>T	XP_024309252.1:p.Arg194Ile
XM_024453485.1:c.581G>T	XP_024309253.1:p.Arg194Ile
XR_427367.3:n.1022G>T
NM_014049.5:c.950G>T MANE Select	NP_054768.2:p.Arg317Ile
NR_033426.2:n.1198G>T