Canonical Allele Identifier: CA354435504

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128621438A>G (hg19) ; chr3:g.128902595A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902595A>G , CM000665.2:g.128902595A>G	GRCh38
NC_000003.11:g.128621438A>G , CM000665.1:g.128621438A>G	GRCh37
NC_000003.10:g.130104128A>G	NCBI36
NG_017064.1:g.28106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.925A>G MANE Select	ENSP00000312618.7:p.Ser309Gly
ENST00000511325.2:n.1003A>G
ENST00000679399.1:c.*819A>G	ENSP00000505434.1:n.*819A>G
ENST00000679431.1:c.*797A>G	ENSP00000506440.1:n.*797A>G
ENST00000679613.1:c.925A>G	ENSP00000504971.1:p.Ser309Gly
ENST00000679715.1:c.556A>G	ENSP00000506228.1:p.Ser186Gly
ENST00000679824.1:c.*2231A>G	ENSP00000505516.1:n.*2231A>G
ENST00000679990.1:n.1160A>G
ENST00000680636.1:c.925A>G	ENSP00000504886.1:p.Ser309Gly
ENST00000680744.1:c.*278A>G	ENSP00000505243.1:n.*278A>G
ENST00000680764.1:c.*2325A>G	ENSP00000505126.1:n.*2325A>G
ENST00000681319.1:n.1003A>G
ENST00000681367.1:c.925A>G	ENSP00000505309.1:p.Ser309Gly
ENST00000681552.1:c.925A>G	ENSP00000505699.1:p.Ser309Gly
ENST00000681583.1:c.925A>G	ENSP00000506340.1:p.Ser309Gly
ENST00000681585.1:c.925A>G	ENSP00000506316.1:p.Ser309Gly
ENST00000681589.1:n.1139A>G
ENST00000681784.1:n.1003A>G
ENST00000681886.1:c.*118A>G	ENSP00000506500.1:n.*118A>G
ENST00000308982.11:c.925A>G	ENSP00000312618.7:p.Ser309Gly
ENST00000505192.5:c.*621A>G	ENSP00000426277.1:n.*621A>G
ENST00000505867.5:c.*725A>G	ENSP00000425346.1:n.*725A>G
ENST00000508971.1:c.214A>G	ENSP00000422683.1:p.Ser72Gly
ENST00000511227.5:c.*819A>G	ENSP00000425226.1:n.*819A>G
ENST00000511526.5:n.426A>G
NM_014049.4:c.925A>G	NP_054768.2:p.Ser309Gly
NR_033426.1:n.1303A>G
XM_011512742.1:c.556A>G	XP_011511044.1:p.Ser186Gly
XR_427367.1:n.997A>G
XM_024453484.1:c.556A>G	XP_024309252.1:p.Ser186Gly
XM_024453485.1:c.556A>G	XP_024309253.1:p.Ser186Gly
XR_427367.3:n.997A>G
NM_014049.5:c.925A>G MANE Select	NP_054768.2:p.Ser309Gly
NR_033426.2:n.1173A>G