Canonical Allele Identifier: CA354435913

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128622923C>A (hg19) ; chr3:g.128904080C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904080C>A , CM000665.2:g.128904080C>A	GRCh38
NC_000003.11:g.128622923C>A , CM000665.1:g.128622923C>A	GRCh37
NC_000003.10:g.130105613C>A	NCBI36
NG_017064.1:g.29591C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.977C>A MANE Select	ENSP00000312618.7:p.Ala326Asp
ENST00000511325.2:n.1055C>A
ENST00000679399.1:c.*871C>A	ENSP00000505434.1:n.*871C>A
ENST00000679431.1:c.*853C>A	ENSP00000506440.1:n.*853C>A
ENST00000679613.1:c.977C>A	ENSP00000504971.1:p.Ala326Asp
ENST00000679715.1:c.608C>A	ENSP00000506228.1:p.Ala203Asp
ENST00000679824.1:c.*2283C>A	ENSP00000505516.1:n.*2283C>A
ENST00000679990.1:n.1212C>A
ENST00000680636.1:c.977C>A	ENSP00000504886.1:p.Ala326Asp
ENST00000680744.1:c.*330C>A	ENSP00000505243.1:n.*330C>A
ENST00000680764.1:c.*2381C>A	ENSP00000505126.1:n.*2381C>A
ENST00000681319.1:n.1055C>A
ENST00000681367.1:c.977C>A	ENSP00000505309.1:p.Ala326Asp
ENST00000681552.1:c.977C>A	ENSP00000505699.1:p.Ala326Asp
ENST00000681583.1:c.977C>A	ENSP00000506340.1:p.Ala326Asp
ENST00000681585.1:c.977C>A	ENSP00000506316.1:p.Ala326Asp
ENST00000681589.1:n.1191C>A
ENST00000681784.1:n.1055C>A
ENST00000681886.1:c.*170C>A	ENSP00000506500.1:n.*170C>A
ENST00000308982.11:c.977C>A	ENSP00000312618.7:p.Ala326Asp
ENST00000505192.5:c.*673C>A	ENSP00000426277.1:n.*673C>A
ENST00000505867.5:c.*777C>A	ENSP00000425346.1:n.*777C>A
ENST00000508971.1:c.266C>A	ENSP00000422683.1:p.Ala89Asp
ENST00000511227.5:c.*871C>A	ENSP00000425226.1:n.*871C>A
ENST00000511526.5:n.482C>A
NM_014049.4:c.977C>A	NP_054768.2:p.Ala326Asp
NR_033426.1:n.1355C>A
XM_011512742.1:c.608C>A	XP_011511044.1:p.Ala203Asp
XR_427367.1:n.1053C>A
XM_024453484.1:c.608C>A	XP_024309252.1:p.Ala203Asp
XM_024453485.1:c.608C>A	XP_024309253.1:p.Ala203Asp
XR_427367.3:n.1053C>A
NM_014049.5:c.977C>A MANE Select	NP_054768.2:p.Ala326Asp
NR_033426.2:n.1225C>A