Canonical Allele Identifier: CA340818155
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761270C>G , CM000663.2:g.75761270C>G GRCh38
NC_000001.10:g.76226955C>G , CM000663.1:g.76226955C>G GRCh37
NC_000001.9:g.75999543C>G NCBI36
NG_007045.2:g.41913C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1094C>G MANE Select ENSP00000359878.5:p.Ala365Gly
ENST00000473018.3:n.3218C>G
ENST00000532207.6:n.2105C>G
ENST00000541113.6:c.998C>G ENSP00000442324.2:p.Ala333Gly
ENST00000679509.1:n.2056C>G
ENST00000679530.1:c.*862C>G ENSP00000506454.1:n.*862C>G
ENST00000679615.1:n.3109C>G
ENST00000679687.1:c.656C>G ENSP00000506598.1:p.Ala219Gly
ENST00000679704.1:c.*860C>G ENSP00000505117.1:n.*860C>G
ENST00000679709.1:c.*1057C>G ENSP00000506623.1:n.*1057C>G
ENST00000679976.1:c.*678C>G ENSP00000505565.1:n.*678C>G
ENST00000680166.1:n.4383C>G
ENST00000680315.1:n.977C>G
ENST00000680517.1:c.*482C>G ENSP00000505803.1:n.*482C>G
ENST00000680582.1:n.2056C>G
ENST00000680613.1:c.*587C>G ENSP00000506114.1:n.*587C>G
ENST00000680662.1:c.*1008C>G ENSP00000505080.1:n.*1008C>G
ENST00000680691.1:c.*757C>G ENSP00000506487.1:n.*757C>G
ENST00000680694.1:c.*682C>G ENSP00000505658.1:n.*682C>G
ENST00000680743.1:c.*883C>G ENSP00000505073.1:n.*883C>G
ENST00000680749.1:c.*379C>G ENSP00000505122.1:n.*379C>G
ENST00000680798.1:c.*569C>G ENSP00000505670.1:n.*569C>G
ENST00000680805.1:c.953C>G ENSP00000505447.1:p.Ala318Gly
ENST00000680844.1:c.*878C>G ENSP00000506541.1:n.*878C>G
ENST00000680948.1:c.*961C>G ENSP00000505441.1:n.*961C>G
ENST00000680964.1:c.*187C>G ENSP00000505961.1:n.*187C>G
ENST00000681037.1:c.*2578C>G ENSP00000506025.1:n.*2578C>G
ENST00000681063.1:c.*363C>G ENSP00000506616.1:n.*363C>G
ENST00000681209.1:c.*749C>G ENSP00000505877.1:n.*749C>G
ENST00000681278.1:n.1796C>G
ENST00000681289.1:n.5089C>G
ENST00000681361.1:c.*761C>G ENSP00000506679.1:n.*761C>G
ENST00000681430.1:c.*187C>G ENSP00000506301.1:n.*187C>G
ENST00000681446.1:c.*798C>G ENSP00000506244.1:n.*798C>G
ENST00000681450.1:c.*765C>G ENSP00000505660.1:n.*765C>G
ENST00000681548.1:c.*680C>G ENSP00000505275.1:n.*680C>G
ENST00000681616.1:c.*753C>G ENSP00000505111.1:n.*753C>G
ENST00000681621.1:c.*678C>G ENSP00000505770.1:n.*678C>G
ENST00000681680.1:n.3189C>G
ENST00000681720.1:c.*549C>G ENSP00000505438.1:n.*549C>G
ENST00000681730.1:n.1316C>G
ENST00000681790.1:c.836C>G ENSP00000505130.1:p.Ala279Gly
ENST00000681837.1:n.1710C>G
ENST00000681913.1:n.3340C>G
ENST00000681916.1:c.*862C>G ENSP00000506477.1:n.*862C>G
ENST00000681930.1:n.3218C>G
ENST00000370834.9:c.1193C>G ENSP00000359871.5:p.Ala398Gly
ENST00000370841.8:c.1094C>G ENSP00000359878.4:p.Ala365Gly
ENST00000420607.6:c.1106C>G ENSP00000409612.2:p.Ala369Gly
ENST00000481374.1:n.367C>G
ENST00000525808.5:c.*680C>G ENSP00000434823.1:n.*680C>G
ENST00000526129.5:c.*878C>G ENSP00000434092.1:n.*878C>G
ENST00000526196.5:c.*862C>G ENSP00000431953.1:n.*862C>G
ENST00000528016.1:c.160-7907C>G ENSP00000434284.1:n.160-7907C>G
ENST00000529059.5:n.1003C>G
ENST00000541113.5:c.986C>G ENSP00000442324.1:p.Ala329Gly
NM_000016.5:c.1094C>G NP_000007.1:p.Ala365Gly
NM_001127328.2:c.1106C>G NP_001120800.1:p.Ala369Gly
NM_001286042.1:c.986C>G NP_001272971.1:p.Ala329Gly
NM_001286043.1:c.1193C>G NP_001272972.1:p.Ala398Gly
NM_001286044.1:c.527C>G NP_001272973.1:p.Ala176Gly
NM_000016.6:c.1094C>G MANE Select NP_000007.1:p.Ala365Gly
NM_001127328.3:c.1106C>G NP_001120800.1:p.Ala369Gly
NM_001286042.2:c.986C>G NP_001272971.1:p.Ala329Gly
NM_001286043.2:c.1193C>G NP_001272972.1:p.Ala398Gly
NM_001286044.2:c.527C>G NP_001272973.1:p.Ala176Gly