Canonical Allele Identifier: CA340818341
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761357C>A , CM000663.2:g.75761357C>A GRCh38
NC_000001.10:g.76227042C>A , CM000663.1:g.76227042C>A GRCh37
NC_000001.9:g.75999630C>A NCBI36
NG_007045.2:g.42000C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1181C>A MANE Select ENSP00000359878.5:p.Ala394Asp
ENST00000473018.3:n.3305C>A
ENST00000532207.6:n.2192C>A
ENST00000541113.6:c.1085C>A ENSP00000442324.2:p.Ala362Asp
ENST00000679509.1:n.2143C>A
ENST00000679530.1:c.*949C>A ENSP00000506454.1:n.*949C>A
ENST00000679615.1:n.3196C>A
ENST00000679687.1:c.743C>A ENSP00000506598.1:p.Ala248Asp
ENST00000679704.1:c.*947C>A ENSP00000505117.1:n.*947C>A
ENST00000679709.1:c.*1144C>A ENSP00000506623.1:n.*1144C>A
ENST00000679976.1:c.*765C>A ENSP00000505565.1:n.*765C>A
ENST00000680166.1:n.4470C>A
ENST00000680315.1:n.1064C>A
ENST00000680517.1:c.*569C>A ENSP00000505803.1:n.*569C>A
ENST00000680582.1:n.2143C>A
ENST00000680613.1:c.*674C>A ENSP00000506114.1:n.*674C>A
ENST00000680662.1:c.*1095C>A ENSP00000505080.1:n.*1095C>A
ENST00000680691.1:c.*844C>A ENSP00000506487.1:n.*844C>A
ENST00000680694.1:c.*769C>A ENSP00000505658.1:n.*769C>A
ENST00000680743.1:c.*970C>A ENSP00000505073.1:n.*970C>A
ENST00000680749.1:c.*466C>A ENSP00000505122.1:n.*466C>A
ENST00000680798.1:c.*656C>A ENSP00000505670.1:n.*656C>A
ENST00000680805.1:c.1040C>A ENSP00000505447.1:p.Ala347Asp
ENST00000680844.1:c.*965C>A ENSP00000506541.1:n.*965C>A
ENST00000680948.1:c.*1048C>A ENSP00000505441.1:n.*1048C>A
ENST00000680964.1:c.*274C>A ENSP00000505961.1:n.*274C>A
ENST00000681037.1:c.*2665C>A ENSP00000506025.1:n.*2665C>A
ENST00000681063.1:c.*450C>A ENSP00000506616.1:n.*450C>A
ENST00000681209.1:c.*836C>A ENSP00000505877.1:n.*836C>A
ENST00000681278.1:n.1883C>A
ENST00000681289.1:n.5176C>A
ENST00000681361.1:c.*848C>A ENSP00000506679.1:n.*848C>A
ENST00000681430.1:c.*274C>A ENSP00000506301.1:n.*274C>A
ENST00000681446.1:c.*885C>A ENSP00000506244.1:n.*885C>A
ENST00000681450.1:c.*852C>A ENSP00000505660.1:n.*852C>A
ENST00000681548.1:c.*767C>A ENSP00000505275.1:n.*767C>A
ENST00000681616.1:c.*840C>A ENSP00000505111.1:n.*840C>A
ENST00000681621.1:c.*765C>A ENSP00000505770.1:n.*765C>A
ENST00000681680.1:n.3276C>A
ENST00000681720.1:c.*636C>A ENSP00000505438.1:n.*636C>A
ENST00000681730.1:n.1403C>A
ENST00000681790.1:c.923C>A ENSP00000505130.1:p.Ala308Asp
ENST00000681837.1:n.1797C>A
ENST00000681913.1:n.3427C>A
ENST00000681916.1:c.*949C>A ENSP00000506477.1:n.*949C>A
ENST00000681930.1:n.3305C>A
ENST00000370834.9:c.1280C>A ENSP00000359871.5:p.Ala427Asp
ENST00000370841.8:c.1181C>A ENSP00000359878.4:p.Ala394Asp
ENST00000420607.6:c.1193C>A ENSP00000409612.2:p.Ala398Asp
ENST00000481374.1:n.454C>A
ENST00000525808.5:c.*767C>A ENSP00000434823.1:n.*767C>A
ENST00000526129.5:c.*965C>A ENSP00000434092.1:n.*965C>A
ENST00000526196.5:c.*949C>A ENSP00000431953.1:n.*949C>A
ENST00000528016.1:c.160-7820C>A ENSP00000434284.1:n.160-7820C>A
ENST00000529059.5:n.1090C>A
ENST00000541113.5:c.1073C>A ENSP00000442324.1:p.Ala358Asp
NM_000016.5:c.1181C>A NP_000007.1:p.Ala394Asp
NM_001127328.2:c.1193C>A NP_001120800.1:p.Ala398Asp
NM_001286042.1:c.1073C>A NP_001272971.1:p.Ala358Asp
NM_001286043.1:c.1280C>A NP_001272972.1:p.Ala427Asp
NM_001286044.1:c.614C>A NP_001272973.1:p.Ala205Asp
NM_000016.6:c.1181C>A MANE Select NP_000007.1:p.Ala394Asp
NM_001127328.3:c.1193C>A NP_001120800.1:p.Ala398Asp
NM_001286042.2:c.1073C>A NP_001272971.1:p.Ala358Asp
NM_001286043.2:c.1280C>A NP_001272972.1:p.Ala427Asp
NM_001286044.2:c.614C>A NP_001272973.1:p.Ala205Asp