Canonical Allele Identifier: CA1142226152
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761221C= , CM000663.2:g.75761221C= GRCh38
NC_000001.10:g.76226906C= , CM000663.1:g.76226906C= GRCh37
NC_000001.9:g.75999494C= NCBI36
NG_007045.2:g.41864C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1045C= MANE Select ENSP00000359878.5:p.Arg349=
ENST00000473018.3:n.3169C=
ENST00000532207.6:n.2056C=
ENST00000541113.6:c.949C= ENSP00000442324.2:p.Arg317=
ENST00000679509.1:n.2007C=
ENST00000679530.1:c.*813C= ENSP00000506454.1:n.*813C=
ENST00000679615.1:n.3060C=
ENST00000679687.1:c.607C= ENSP00000506598.1:p.Arg203=
ENST00000679704.1:c.*811C= ENSP00000505117.1:n.*811C=
ENST00000679709.1:c.*1008C= ENSP00000506623.1:n.*1008C=
ENST00000679976.1:c.*629C= ENSP00000505565.1:n.*629C=
ENST00000680166.1:n.4334C=
ENST00000680315.1:n.928C=
ENST00000680517.1:c.*433C= ENSP00000505803.1:n.*433C=
ENST00000680582.1:n.2007C=
ENST00000680613.1:c.*538C= ENSP00000506114.1:n.*538C=
ENST00000680662.1:c.*959C= ENSP00000505080.1:n.*959C=
ENST00000680691.1:c.*708C= ENSP00000506487.1:n.*708C=
ENST00000680694.1:c.*633C= ENSP00000505658.1:n.*633C=
ENST00000680743.1:c.*834C= ENSP00000505073.1:n.*834C=
ENST00000680749.1:c.*330C= ENSP00000505122.1:n.*330C=
ENST00000680798.1:c.*520C= ENSP00000505670.1:n.*520C=
ENST00000680805.1:c.904C= ENSP00000505447.1:p.Arg302=
ENST00000680844.1:c.*829C= ENSP00000506541.1:n.*829C=
ENST00000680948.1:c.*912C= ENSP00000505441.1:n.*912C=
ENST00000680964.1:c.*138C= ENSP00000505961.1:n.*138C=
ENST00000681037.1:c.*2529C= ENSP00000506025.1:n.*2529C=
ENST00000681063.1:c.*314C= ENSP00000506616.1:n.*314C=
ENST00000681209.1:c.*700C= ENSP00000505877.1:n.*700C=
ENST00000681278.1:n.1747C=
ENST00000681289.1:n.5040C=
ENST00000681361.1:c.*712C= ENSP00000506679.1:n.*712C=
ENST00000681430.1:c.*138C= ENSP00000506301.1:n.*138C=
ENST00000681446.1:c.*749C= ENSP00000506244.1:n.*749C=
ENST00000681450.1:c.*716C= ENSP00000505660.1:n.*716C=
ENST00000681548.1:c.*631C= ENSP00000505275.1:n.*631C=
ENST00000681616.1:c.*704C= ENSP00000505111.1:n.*704C=
ENST00000681621.1:c.*629C= ENSP00000505770.1:n.*629C=
ENST00000681680.1:n.3140C=
ENST00000681720.1:c.*500C= ENSP00000505438.1:n.*500C=
ENST00000681730.1:n.1267C=
ENST00000681790.1:c.787C= ENSP00000505130.1:p.Arg263=
ENST00000681837.1:n.1661C=
ENST00000681913.1:n.3291C=
ENST00000681916.1:c.*813C= ENSP00000506477.1:n.*813C=
ENST00000681930.1:n.3169C=
ENST00000370834.9:c.1144C= ENSP00000359871.5:p.Arg382=
ENST00000370841.8:c.1045C= ENSP00000359878.4:p.Arg349=
ENST00000420607.6:c.1057C= ENSP00000409612.2:p.Arg353=
ENST00000481374.1:n.318C=
ENST00000525808.5:c.*631C= ENSP00000434823.1:n.*631C=
ENST00000526129.5:c.*829C= ENSP00000434092.1:n.*829C=
ENST00000526196.5:c.*813C= ENSP00000431953.1:n.*813C=
ENST00000528016.1:c.160-7956C= ENSP00000434284.1:n.160-7956C=
ENST00000529059.5:n.954C=
ENST00000534334.5:c.*786C= ENSP00000435584.1:n.*786C=
ENST00000541113.5:c.937C= ENSP00000442324.1:p.Arg313=
NM_000016.5:c.1045C= NP_000007.1:p.Arg349=
NM_001127328.2:c.1057C= NP_001120800.1:p.Arg353=
NM_001286042.1:c.937C= NP_001272971.1:p.Arg313=
NM_001286043.1:c.1144C= NP_001272972.1:p.Arg382=
NM_001286044.1:c.478C= NP_001272973.1:p.Arg160=
NM_000016.6:c.1045C= MANE Select NP_000007.1:p.Arg349=
NM_001127328.3:c.1057C= NP_001120800.1:p.Arg353=
NM_001286042.2:c.937C= NP_001272971.1:p.Arg313=
NM_001286043.2:c.1144C= NP_001272972.1:p.Arg382=
NM_001286044.2:c.478C= NP_001272973.1:p.Arg160=