Canonical Allele Identifier: CA354435518

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128621445T>C (hg19) ; chr3:g.128902602T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902602T>C , CM000665.2:g.128902602T>C	GRCh38
NC_000003.11:g.128621445T>C , CM000665.1:g.128621445T>C	GRCh37
NC_000003.10:g.130104135T>C	NCBI36
NG_017064.1:g.28113T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.932T>C MANE Select	ENSP00000312618.7:p.Val311Ala
ENST00000511325.2:n.1010T>C
ENST00000679399.1:c.*826T>C	ENSP00000505434.1:n.*826T>C
ENST00000679431.1:c.*804T>C	ENSP00000506440.1:n.*804T>C
ENST00000679613.1:c.932T>C	ENSP00000504971.1:p.Val311Ala
ENST00000679715.1:c.563T>C	ENSP00000506228.1:p.Val188Ala
ENST00000679824.1:c.*2238T>C	ENSP00000505516.1:n.*2238T>C
ENST00000679990.1:n.1167T>C
ENST00000680636.1:c.932T>C	ENSP00000504886.1:p.Val311Ala
ENST00000680744.1:c.*285T>C	ENSP00000505243.1:n.*285T>C
ENST00000680764.1:c.*2332T>C	ENSP00000505126.1:n.*2332T>C
ENST00000681319.1:n.1010T>C
ENST00000681367.1:c.932T>C	ENSP00000505309.1:p.Val311Ala
ENST00000681552.1:c.932T>C	ENSP00000505699.1:p.Val311Ala
ENST00000681583.1:c.932T>C	ENSP00000506340.1:p.Val311Ala
ENST00000681585.1:c.932T>C	ENSP00000506316.1:p.Val311Ala
ENST00000681589.1:n.1146T>C
ENST00000681784.1:n.1010T>C
ENST00000681886.1:c.*125T>C	ENSP00000506500.1:n.*125T>C
ENST00000308982.11:c.932T>C	ENSP00000312618.7:p.Val311Ala
ENST00000505192.5:c.*628T>C	ENSP00000426277.1:n.*628T>C
ENST00000505867.5:c.*732T>C	ENSP00000425346.1:n.*732T>C
ENST00000508971.1:c.221T>C	ENSP00000422683.1:p.Val74Ala
ENST00000511227.5:c.*826T>C	ENSP00000425226.1:n.*826T>C
ENST00000511526.5:n.433T>C
NM_014049.4:c.932T>C	NP_054768.2:p.Val311Ala
NR_033426.1:n.1310T>C
XM_011512742.1:c.563T>C	XP_011511044.1:p.Val188Ala
XR_427367.1:n.1004T>C
XM_024453484.1:c.563T>C	XP_024309252.1:p.Val188Ala
XM_024453485.1:c.563T>C	XP_024309253.1:p.Val188Ala
XR_427367.3:n.1004T>C
NM_014049.5:c.932T>C MANE Select	NP_054768.2:p.Val311Ala
NR_033426.2:n.1180T>C