Canonical Allele Identifier: CA435591391
Gene: ACAD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.128621443C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128902600C>A , CM000665.2:g.128902600C>A GRCh38
NC_000003.11:g.128621443C>A , CM000665.1:g.128621443C>A GRCh37
NC_000003.10:g.130104133C>A NCBI36
NG_017064.1:g.28111C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.930C>A MANE Select ENSP00000312618.7:p.Val310=
ENST00000511325.2:n.1008C>A
ENST00000679399.1:c.*824C>A ENSP00000505434.1:n.*824C>A
ENST00000679431.1:c.*802C>A ENSP00000506440.1:n.*802C>A
ENST00000679613.1:c.930C>A ENSP00000504971.1:p.Val310=
ENST00000679715.1:c.561C>A ENSP00000506228.1:p.Val187=
ENST00000679824.1:c.*2236C>A ENSP00000505516.1:n.*2236C>A
ENST00000679990.1:n.1165C>A
ENST00000680636.1:c.930C>A ENSP00000504886.1:p.Val310=
ENST00000680744.1:c.*283C>A ENSP00000505243.1:n.*283C>A
ENST00000680764.1:c.*2330C>A ENSP00000505126.1:n.*2330C>A
ENST00000681319.1:n.1008C>A
ENST00000681367.1:c.930C>A ENSP00000505309.1:p.Val310=
ENST00000681552.1:c.930C>A ENSP00000505699.1:p.Val310=
ENST00000681583.1:c.930C>A ENSP00000506340.1:p.Val310=
ENST00000681585.1:c.930C>A ENSP00000506316.1:p.Val310=
ENST00000681589.1:n.1144C>A
ENST00000681784.1:n.1008C>A
ENST00000681886.1:c.*123C>A ENSP00000506500.1:n.*123C>A
ENST00000308982.11:c.930C>A ENSP00000312618.7:p.Val310=
ENST00000505192.5:c.*626C>A ENSP00000426277.1:n.*626C>A
ENST00000505867.5:c.*730C>A ENSP00000425346.1:n.*730C>A
ENST00000508971.1:c.219C>A ENSP00000422683.1:p.Val73=
ENST00000511227.5:c.*824C>A ENSP00000425226.1:n.*824C>A
ENST00000511526.5:n.431C>A
NM_014049.4:c.930C>A NP_054768.2:p.Val310=
NR_033426.1:n.1308C>A
XM_011512742.1:c.561C>A XP_011511044.1:p.Val187=
XR_427367.1:n.1002C>A
XM_024453484.1:c.561C>A XP_024309252.1:p.Val187=
XM_024453485.1:c.561C>A XP_024309253.1:p.Val187=
XR_427367.3:n.1002C>A
NM_014049.5:c.930C>A MANE Select NP_054768.2:p.Val310=
NR_033426.2:n.1178C>A