Canonical Allele Identifier: CA354438629

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628257T>A (hg19) ; chr3:g.128909414T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909414T>A , CM000665.2:g.128909414T>A	GRCh38
NC_000003.11:g.128628257T>A , CM000665.1:g.128628257T>A	GRCh37
NC_000003.10:g.130110947T>A	NCBI36
NG_017064.1:g.34925T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1556T>A MANE Select	ENSP00000312618.7:p.Phe519Tyr
ENST00000511325.2:n.1634T>A
ENST00000679399.1:c.*1727T>A	ENSP00000505434.1:n.*1727T>A
ENST00000679431.1:c.*1432T>A	ENSP00000506440.1:n.*1432T>A
ENST00000679613.1:c.1556T>A	ENSP00000504971.1:p.Phe519Tyr
ENST00000679715.1:c.1187T>A	ENSP00000506228.1:p.Phe396Tyr
ENST00000679824.1:c.*2862T>A	ENSP00000505516.1:n.*2862T>A
ENST00000679990.1:n.1791T>A
ENST00000680636.1:c.1556T>A	ENSP00000504886.1:p.Phe519Tyr
ENST00000680638.1:n.1309T>A
ENST00000680744.1:c.*909T>A	ENSP00000505243.1:n.*909T>A
ENST00000680764.1:c.*2960T>A	ENSP00000505126.1:n.*2960T>A
ENST00000681319.1:n.2342T>A
ENST00000681367.1:c.1556T>A	ENSP00000505309.1:p.Phe519Tyr
ENST00000681552.1:c.1150-3093T>A	ENSP00000505699.1:n.1150-3093T>A
ENST00000681583.1:c.1556T>A	ENSP00000506340.1:p.Phe519Tyr
ENST00000681585.1:c.*175T>A	ENSP00000506316.1:n.*175T>A
ENST00000681784.1:n.1634T>A
ENST00000681886.1:c.*749T>A	ENSP00000506500.1:n.*749T>A
ENST00000308982.11:c.1556T>A	ENSP00000312618.7:p.Phe519Tyr
ENST00000505867.5:c.*1356T>A	ENSP00000425346.1:n.*1356T>A
ENST00000508971.1:c.845T>A	ENSP00000422683.1:p.Phe282Tyr
ENST00000511227.5:c.*1450T>A	ENSP00000425226.1:n.*1450T>A
ENST00000511325.1:n.537T>A
ENST00000511526.5:n.1089T>A
NM_014049.4:c.1556T>A	NP_054768.2:p.Phe519Tyr
NR_033426.1:n.1934T>A
XM_011512742.1:c.1187T>A	XP_011511044.1:p.Phe396Tyr
XM_024453484.1:c.1187T>A	XP_024309252.1:p.Phe396Tyr
XM_024453485.1:c.1187T>A	XP_024309253.1:p.Phe396Tyr
XR_427367.3:n.1632T>A
NM_014049.5:c.1556T>A MANE Select	NP_054768.2:p.Phe519Tyr
NR_033426.2:n.1804T>A