Canonical Allele Identifier: CA1176721462
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749508C= , CM000663.2:g.75749508C= GRCh38
NC_000001.10:g.76215193C= , CM000663.1:g.76215193C= GRCh37
NC_000001.9:g.75987781C= NCBI36
NG_007045.2:g.30151C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.798C= MANE Select ENSP00000359878.5:p.Asp266=
ENST00000473018.3:n.2922C=
ENST00000532207.6:n.1687C=
ENST00000541113.6:c.798C= ENSP00000442324.2:p.Asp266=
ENST00000679509.1:n.1760C=
ENST00000679530.1:c.*566C= ENSP00000506454.1:n.*566C=
ENST00000679615.1:n.2813C=
ENST00000679687.1:c.360C= ENSP00000506598.1:p.Asp120=
ENST00000679704.1:c.*564C= ENSP00000505117.1:n.*564C=
ENST00000679709.1:c.*761C= ENSP00000506623.1:n.*761C=
ENST00000679976.1:c.*382C= ENSP00000505565.1:n.*382C=
ENST00000680166.1:n.4087C=
ENST00000680517.1:c.*186C= ENSP00000505803.1:n.*186C=
ENST00000680582.1:n.1760C=
ENST00000680613.1:c.*169C= ENSP00000506114.1:n.*169C=
ENST00000680662.1:c.*712C= ENSP00000505080.1:n.*712C=
ENST00000680691.1:c.*461C= ENSP00000506487.1:n.*461C=
ENST00000680694.1:c.*386C= ENSP00000505658.1:n.*386C=
ENST00000680743.1:c.*465C= ENSP00000505073.1:n.*465C=
ENST00000680749.1:c.*83C= ENSP00000505122.1:n.*83C=
ENST00000680798.1:c.*273C= ENSP00000505670.1:n.*273C=
ENST00000680805.1:c.709-943C= ENSP00000505447.1:n.709-943C=
ENST00000680844.1:c.*582C= ENSP00000506541.1:n.*582C=
ENST00000680948.1:c.*665C= ENSP00000505441.1:n.*665C=
ENST00000680964.1:c.798C= ENSP00000505961.1:p.Asp266=
ENST00000681037.1:c.*2282C= ENSP00000506025.1:n.*2282C=
ENST00000681063.1:c.600-943C= ENSP00000506616.1:n.600-943C=
ENST00000681209.1:c.*453C= ENSP00000505877.1:n.*453C=
ENST00000681278.1:n.1155C=
ENST00000681289.1:n.4793C=
ENST00000681361.1:c.*465C= ENSP00000506679.1:n.*465C=
ENST00000681430.1:c.798C= ENSP00000506301.1:p.Asp266=
ENST00000681446.1:c.*380C= ENSP00000506244.1:n.*380C=
ENST00000681450.1:c.*469C= ENSP00000505660.1:n.*469C=
ENST00000681548.1:c.*384C= ENSP00000505275.1:n.*384C=
ENST00000681616.1:c.*457C= ENSP00000505111.1:n.*457C=
ENST00000681621.1:c.*382C= ENSP00000505770.1:n.*382C=
ENST00000681680.1:n.2893C=
ENST00000681720.1:c.*253C= ENSP00000505438.1:n.*253C=
ENST00000681730.1:n.1020C=
ENST00000681790.1:c.540C= ENSP00000505130.1:p.Asp180=
ENST00000681837.1:n.1414C=
ENST00000681913.1:n.2922C=
ENST00000681916.1:c.*566C= ENSP00000506477.1:n.*566C=
ENST00000681930.1:n.2922C=
ENST00000370834.9:c.897C= ENSP00000359871.5:p.Asp299=
ENST00000370841.8:c.798C= ENSP00000359878.4:p.Asp266=
ENST00000420607.6:c.810C= ENSP00000409612.2:p.Asp270=
ENST00000525808.5:c.*384C= ENSP00000434823.1:n.*384C=
ENST00000526129.5:c.*582C= ENSP00000434092.1:n.*582C=
ENST00000526196.5:c.*566C= ENSP00000431953.1:n.*566C=
ENST00000526930.1:n.571C=
ENST00000528016.1:c.12C= ENSP00000434284.1:p.Asp4=
ENST00000529059.5:n.707C=
ENST00000530953.6:c.*295C= ENSP00000431372.1:n.*295C=
ENST00000532207.5:n.528C=
ENST00000532509.5:c.*562C= ENSP00000432522.1:n.*562C=
ENST00000534334.5:c.*382C= ENSP00000435584.1:n.*382C=
ENST00000541113.5:c.690C= ENSP00000442324.1:p.Asp230=
NM_000016.5:c.798C= NP_000007.1:p.Asp266=
NM_001127328.2:c.810C= NP_001120800.1:p.Asp270=
NM_001286042.1:c.690C= NP_001272971.1:p.Asp230=
NM_001286043.1:c.897C= NP_001272972.1:p.Asp299=
NM_001286044.1:c.231C= NP_001272973.1:p.Asp77=
NM_000016.6:c.798C= MANE Select NP_000007.1:p.Asp266=
NM_001127328.3:c.810C= NP_001120800.1:p.Asp270=
NM_001286042.2:c.690C= NP_001272971.1:p.Asp230=
NM_001286043.2:c.897C= NP_001272972.1:p.Asp299=
NM_001286044.2:c.231C= NP_001272973.1:p.Asp77=