Canonical Allele Identifier: CA435591752

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128622924C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904081C>A , CM000665.2:g.128904081C>A	GRCh38
NC_000003.11:g.128622924C>A , CM000665.1:g.128622924C>A	GRCh37
NC_000003.10:g.130105614C>A	NCBI36
NG_017064.1:g.29592C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.978C>A MANE Select	ENSP00000312618.7:p.Ala326=
ENST00000511325.2:n.1056C>A
ENST00000679399.1:c.*872C>A	ENSP00000505434.1:n.*872C>A
ENST00000679431.1:c.*854C>A	ENSP00000506440.1:n.*854C>A
ENST00000679613.1:c.978C>A	ENSP00000504971.1:p.Ala326=
ENST00000679715.1:c.609C>A	ENSP00000506228.1:p.Ala203=
ENST00000679824.1:c.*2284C>A	ENSP00000505516.1:n.*2284C>A
ENST00000679990.1:n.1213C>A
ENST00000680636.1:c.978C>A	ENSP00000504886.1:p.Ala326=
ENST00000680744.1:c.*331C>A	ENSP00000505243.1:n.*331C>A
ENST00000680764.1:c.*2382C>A	ENSP00000505126.1:n.*2382C>A
ENST00000681319.1:n.1056C>A
ENST00000681367.1:c.978C>A	ENSP00000505309.1:p.Ala326=
ENST00000681552.1:c.978C>A	ENSP00000505699.1:p.Ala326=
ENST00000681583.1:c.978C>A	ENSP00000506340.1:p.Ala326=
ENST00000681585.1:c.978C>A	ENSP00000506316.1:p.Ala326=
ENST00000681589.1:n.1192C>A
ENST00000681784.1:n.1056C>A
ENST00000681886.1:c.*171C>A	ENSP00000506500.1:n.*171C>A
ENST00000308982.11:c.978C>A	ENSP00000312618.7:p.Ala326=
ENST00000505192.5:c.*674C>A	ENSP00000426277.1:n.*674C>A
ENST00000505867.5:c.*778C>A	ENSP00000425346.1:n.*778C>A
ENST00000508971.1:c.267C>A	ENSP00000422683.1:p.Ala89=
ENST00000511227.5:c.*872C>A	ENSP00000425226.1:n.*872C>A
ENST00000511526.5:n.483C>A
NM_014049.4:c.978C>A	NP_054768.2:p.Ala326=
NR_033426.1:n.1356C>A
XM_011512742.1:c.609C>A	XP_011511044.1:p.Ala203=
XR_427367.1:n.1054C>A
XM_024453484.1:c.609C>A	XP_024309252.1:p.Ala203=
XM_024453485.1:c.609C>A	XP_024309253.1:p.Ala203=
XR_427367.3:n.1054C>A
NM_014049.5:c.978C>A MANE Select	NP_054768.2:p.Ala326=
NR_033426.2:n.1226C>A