Canonical Allele Identifier: CA1176720061
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745904T= , CM000663.2:g.75745904T= GRCh38
NC_000001.10:g.76211589T= , CM000663.1:g.76211589T= GRCh37
NC_000001.9:g.75984177T= NCBI36
NG_007045.2:g.26547T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.698T= MANE Select ENSP00000359878.5:p.Ile233=
ENST00000473018.3:n.2822T=
ENST00000532207.6:n.1587T=
ENST00000541113.6:c.698T= ENSP00000442324.2:p.Ile233=
ENST00000679509.1:n.1660T=
ENST00000679530.1:c.*466T= ENSP00000506454.1:n.*466T=
ENST00000679615.1:n.2724-3515T=
ENST00000679687.1:c.260T= ENSP00000506598.1:p.Ile87=
ENST00000679704.1:c.*464T= ENSP00000505117.1:n.*464T=
ENST00000679709.1:c.*661T= ENSP00000506623.1:n.*661T=
ENST00000679976.1:c.*282T= ENSP00000505565.1:n.*282T=
ENST00000680166.1:n.3987T=
ENST00000680517.1:c.*97-3515T= ENSP00000505803.1:n.*97-3515T=
ENST00000680582.1:n.1660T=
ENST00000680613.1:c.*69T= ENSP00000506114.1:n.*69T=
ENST00000680662.1:c.*612T= ENSP00000505080.1:n.*612T=
ENST00000680691.1:c.*361T= ENSP00000506487.1:n.*361T=
ENST00000680694.1:c.*286T= ENSP00000505658.1:n.*286T=
ENST00000680743.1:c.*365T= ENSP00000505073.1:n.*365T=
ENST00000680749.1:c.600-3515T= ENSP00000505122.1:n.600-3515T=
ENST00000680798.1:c.*184-3515T= ENSP00000505670.1:n.*184-3515T=
ENST00000680805.1:c.698T= ENSP00000505447.1:p.Ile233=
ENST00000680844.1:c.*482T= ENSP00000506541.1:n.*482T=
ENST00000680948.1:c.*565T= ENSP00000505441.1:n.*565T=
ENST00000680964.1:c.698T= ENSP00000505961.1:p.Ile233=
ENST00000681037.1:c.*2182T= ENSP00000506025.1:n.*2182T=
ENST00000681063.1:c.600-4547T= ENSP00000506616.1:n.600-4547T=
ENST00000681209.1:c.*364-3515T= ENSP00000505877.1:n.*364-3515T=
ENST00000681278.1:n.1055T=
ENST00000681289.1:n.4693T=
ENST00000681361.1:c.*365T= ENSP00000506679.1:n.*365T=
ENST00000681430.1:c.698T= ENSP00000506301.1:p.Ile233=
ENST00000681446.1:c.*280T= ENSP00000506244.1:n.*280T=
ENST00000681450.1:c.*369T= ENSP00000505660.1:n.*369T=
ENST00000681548.1:c.*284T= ENSP00000505275.1:n.*284T=
ENST00000681616.1:c.*368-3515T= ENSP00000505111.1:n.*368-3515T=
ENST00000681621.1:c.*282T= ENSP00000505770.1:n.*282T=
ENST00000681680.1:n.2793T=
ENST00000681720.1:c.*153T= ENSP00000505438.1:n.*153T=
ENST00000681730.1:n.920T=
ENST00000681790.1:c.440T= ENSP00000505130.1:p.Ile147=
ENST00000681837.1:n.1314T=
ENST00000681913.1:n.2822T=
ENST00000681916.1:c.*466T= ENSP00000506477.1:n.*466T=
ENST00000681930.1:n.2822T=
ENST00000370834.9:c.797T= ENSP00000359871.5:p.Ile266=
ENST00000370841.8:c.698T= ENSP00000359878.4:p.Ile233=
ENST00000420607.6:c.710T= ENSP00000409612.2:p.Ile237=
ENST00000525808.5:c.*284T= ENSP00000434823.1:n.*284T=
ENST00000526129.5:c.*482T= ENSP00000434092.1:n.*482T=
ENST00000526196.5:c.*466T= ENSP00000431953.1:n.*466T=
ENST00000526930.1:n.471T=
ENST00000529059.5:n.607T=
ENST00000530953.6:c.*195T= ENSP00000431372.1:n.*195T=
ENST00000532207.5:n.428T=
ENST00000532509.5:c.*462T= ENSP00000432522.1:n.*462T=
ENST00000534334.5:c.*282T= ENSP00000435584.1:n.*282T=
ENST00000541113.5:c.590T= ENSP00000442324.1:p.Ile197=
NM_000016.5:c.698T= NP_000007.1:p.Ile233=
NM_001127328.2:c.710T= NP_001120800.1:p.Ile237=
NM_001286042.1:c.590T= NP_001272971.1:p.Ile197=
NM_001286043.1:c.797T= NP_001272972.1:p.Ile266=
NM_001286044.1:c.131T= NP_001272973.1:p.Ile44=
NM_000016.6:c.698T= MANE Select NP_000007.1:p.Ile233=
NM_001127328.3:c.710T= NP_001120800.1:p.Ile237=
NM_001286042.2:c.590T= NP_001272971.1:p.Ile197=
NM_001286043.2:c.797T= NP_001272972.1:p.Ile266=
NM_001286044.2:c.131T= NP_001272973.1:p.Ile44=