Canonical Allele Identifier: CA354438521

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628204T>A (hg19) ; chr3:g.128909361T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909361T>A , CM000665.2:g.128909361T>A	GRCh38
NC_000003.11:g.128628204T>A , CM000665.1:g.128628204T>A	GRCh37
NC_000003.10:g.130110894T>A	NCBI36
NG_017064.1:g.34872T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1503T>A MANE Select	ENSP00000312618.7:p.Phe501Leu
ENST00000511325.2:n.1581T>A
ENST00000679399.1:c.*1674T>A	ENSP00000505434.1:n.*1674T>A
ENST00000679431.1:c.*1379T>A	ENSP00000506440.1:n.*1379T>A
ENST00000679613.1:c.1503T>A	ENSP00000504971.1:p.Phe501Leu
ENST00000679715.1:c.1134T>A	ENSP00000506228.1:p.Phe378Leu
ENST00000679824.1:c.*2809T>A	ENSP00000505516.1:n.*2809T>A
ENST00000679990.1:n.1738T>A
ENST00000680636.1:c.1503T>A	ENSP00000504886.1:p.Phe501Leu
ENST00000680638.1:n.1256T>A
ENST00000680744.1:c.*856T>A	ENSP00000505243.1:n.*856T>A
ENST00000680764.1:c.*2907T>A	ENSP00000505126.1:n.*2907T>A
ENST00000681319.1:n.2289T>A
ENST00000681367.1:c.1503T>A	ENSP00000505309.1:p.Phe501Leu
ENST00000681552.1:c.1150-3146T>A	ENSP00000505699.1:n.1150-3146T>A
ENST00000681583.1:c.1503T>A	ENSP00000506340.1:p.Phe501Leu
ENST00000681585.1:c.*122T>A	ENSP00000506316.1:n.*122T>A
ENST00000681784.1:n.1581T>A
ENST00000681886.1:c.*696T>A	ENSP00000506500.1:n.*696T>A
ENST00000308982.11:c.1503T>A	ENSP00000312618.7:p.Phe501Leu
ENST00000505867.5:c.*1303T>A	ENSP00000425346.1:n.*1303T>A
ENST00000508971.1:c.792T>A	ENSP00000422683.1:p.Phe264Leu
ENST00000511227.5:c.*1397T>A	ENSP00000425226.1:n.*1397T>A
ENST00000511325.1:n.484T>A
ENST00000511526.5:n.1036T>A
NM_014049.4:c.1503T>A	NP_054768.2:p.Phe501Leu
NR_033426.1:n.1881T>A
XM_011512742.1:c.1134T>A	XP_011511044.1:p.Phe378Leu
XM_024453484.1:c.1134T>A	XP_024309252.1:p.Phe378Leu
XM_024453485.1:c.1134T>A	XP_024309253.1:p.Phe378Leu
XR_427367.3:n.1579T>A
NM_014049.5:c.1503T>A MANE Select	NP_054768.2:p.Phe501Leu
NR_033426.2:n.1751T>A