Canonical Allele Identifier: CA340817165
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750526T>A , CM000663.2:g.75750526T>A GRCh38
NC_000001.10:g.76216211T>A , CM000663.1:g.76216211T>A GRCh37
NC_000001.9:g.75988799T>A NCBI36
NG_007045.2:g.31169T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.925T>A MANE Select ENSP00000359878.5:p.Phe309Ile
ENST00000473018.3:n.3049T>A
ENST00000532207.6:n.1814T>A
ENST00000541113.6:c.849+967T>A ENSP00000442324.2:n.849+967T>A
ENST00000679509.1:n.1887T>A
ENST00000679530.1:c.*693T>A ENSP00000506454.1:n.*693T>A
ENST00000679615.1:n.2940T>A
ENST00000679687.1:c.487T>A ENSP00000506598.1:p.Phe163Ile
ENST00000679704.1:c.*691T>A ENSP00000505117.1:n.*691T>A
ENST00000679709.1:c.*888T>A ENSP00000506623.1:n.*888T>A
ENST00000679976.1:c.*509T>A ENSP00000505565.1:n.*509T>A
ENST00000680166.1:n.4214T>A
ENST00000680315.1:n.808T>A
ENST00000680517.1:c.*313T>A ENSP00000505803.1:n.*313T>A
ENST00000680582.1:n.1887T>A
ENST00000680613.1:c.*296T>A ENSP00000506114.1:n.*296T>A
ENST00000680662.1:c.*839T>A ENSP00000505080.1:n.*839T>A
ENST00000680691.1:c.*588T>A ENSP00000506487.1:n.*588T>A
ENST00000680694.1:c.*513T>A ENSP00000505658.1:n.*513T>A
ENST00000680743.1:c.*592T>A ENSP00000505073.1:n.*592T>A
ENST00000680749.1:c.*210T>A ENSP00000505122.1:n.*210T>A
ENST00000680798.1:c.*400T>A ENSP00000505670.1:n.*400T>A
ENST00000680805.1:c.784T>A ENSP00000505447.1:p.Phe262Ile
ENST00000680844.1:c.*709T>A ENSP00000506541.1:n.*709T>A
ENST00000680948.1:c.*792T>A ENSP00000505441.1:n.*792T>A
ENST00000680964.1:c.925T>A ENSP00000505961.1:p.Phe309Ile
ENST00000681037.1:c.*2409T>A ENSP00000506025.1:n.*2409T>A
ENST00000681063.1:c.*72T>A ENSP00000506616.1:n.*72T>A
ENST00000681209.1:c.*580T>A ENSP00000505877.1:n.*580T>A
ENST00000681278.1:n.1282T>A
ENST00000681289.1:n.4920T>A
ENST00000681361.1:c.*592T>A ENSP00000506679.1:n.*592T>A
ENST00000681430.1:c.925T>A ENSP00000506301.1:p.Phe309Ile
ENST00000681446.1:c.*507T>A ENSP00000506244.1:n.*507T>A
ENST00000681450.1:c.*596T>A ENSP00000505660.1:n.*596T>A
ENST00000681548.1:c.*511T>A ENSP00000505275.1:n.*511T>A
ENST00000681616.1:c.*584T>A ENSP00000505111.1:n.*584T>A
ENST00000681621.1:c.*509T>A ENSP00000505770.1:n.*509T>A
ENST00000681680.1:n.3020T>A
ENST00000681720.1:c.*380T>A ENSP00000505438.1:n.*380T>A
ENST00000681730.1:n.1147T>A
ENST00000681790.1:c.667T>A ENSP00000505130.1:p.Phe223Ile
ENST00000681837.1:n.1541T>A
ENST00000681913.1:n.3049T>A
ENST00000681916.1:c.*693T>A ENSP00000506477.1:n.*693T>A
ENST00000681930.1:n.3049T>A
ENST00000370834.9:c.1024T>A ENSP00000359871.5:p.Phe342Ile
ENST00000370841.8:c.925T>A ENSP00000359878.4:p.Phe309Ile
ENST00000420607.6:c.937T>A ENSP00000409612.2:p.Phe313Ile
ENST00000481374.1:n.76T>A
ENST00000525808.5:c.*511T>A ENSP00000434823.1:n.*511T>A
ENST00000526129.5:c.*709T>A ENSP00000434092.1:n.*709T>A
ENST00000526196.5:c.*693T>A ENSP00000431953.1:n.*693T>A
ENST00000528016.1:c.139T>A ENSP00000434284.1:p.Phe47Ile
ENST00000529059.5:n.834T>A
ENST00000532207.5:n.655T>A
ENST00000534334.5:c.*509T>A ENSP00000435584.1:n.*509T>A
ENST00000541113.5:c.817T>A ENSP00000442324.1:p.Phe273Ile
NM_000016.5:c.925T>A NP_000007.1:p.Phe309Ile
NM_001127328.2:c.937T>A NP_001120800.1:p.Phe313Ile
NM_001286042.1:c.817T>A NP_001272971.1:p.Phe273Ile
NM_001286043.1:c.1024T>A NP_001272972.1:p.Phe342Ile
NM_001286044.1:c.358T>A NP_001272973.1:p.Phe120Ile
NM_000016.6:c.925T>A MANE Select NP_000007.1:p.Phe309Ile
NM_001127328.3:c.937T>A NP_001120800.1:p.Phe313Ile
NM_001286042.2:c.817T>A NP_001272971.1:p.Phe273Ile
NM_001286043.2:c.1024T>A NP_001272972.1:p.Phe342Ile
NM_001286044.2:c.358T>A NP_001272973.1:p.Phe120Ile