Canonical Allele Identifier: CA1176721446
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749461G= , CM000663.2:g.75749461G= GRCh38
NC_000001.10:g.76215146G= , CM000663.1:g.76215146G= GRCh37
NC_000001.9:g.75987734G= NCBI36
NG_007045.2:g.30104G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.751G= MANE Select ENSP00000359878.5:p.Val251=
ENST00000473018.3:n.2875G=
ENST00000532207.6:n.1640G=
ENST00000541113.6:c.751G= ENSP00000442324.2:p.Val251=
ENST00000679509.1:n.1713G=
ENST00000679530.1:c.*519G= ENSP00000506454.1:n.*519G=
ENST00000679615.1:n.2766G=
ENST00000679687.1:c.313G= ENSP00000506598.1:p.Val105=
ENST00000679704.1:c.*517G= ENSP00000505117.1:n.*517G=
ENST00000679709.1:c.*714G= ENSP00000506623.1:n.*714G=
ENST00000679976.1:c.*335G= ENSP00000505565.1:n.*335G=
ENST00000680166.1:n.4040G=
ENST00000680517.1:c.*139G= ENSP00000505803.1:n.*139G=
ENST00000680582.1:n.1713G=
ENST00000680613.1:c.*122G= ENSP00000506114.1:n.*122G=
ENST00000680662.1:c.*665G= ENSP00000505080.1:n.*665G=
ENST00000680691.1:c.*414G= ENSP00000506487.1:n.*414G=
ENST00000680694.1:c.*339G= ENSP00000505658.1:n.*339G=
ENST00000680743.1:c.*418G= ENSP00000505073.1:n.*418G=
ENST00000680749.1:c.*36G= ENSP00000505122.1:n.*36G=
ENST00000680798.1:c.*226G= ENSP00000505670.1:n.*226G=
ENST00000680805.1:c.709-990G= ENSP00000505447.1:n.709-990G=
ENST00000680844.1:c.*535G= ENSP00000506541.1:n.*535G=
ENST00000680948.1:c.*618G= ENSP00000505441.1:n.*618G=
ENST00000680964.1:c.751G= ENSP00000505961.1:p.Val251=
ENST00000681037.1:c.*2235G= ENSP00000506025.1:n.*2235G=
ENST00000681063.1:c.600-990G= ENSP00000506616.1:n.600-990G=
ENST00000681209.1:c.*406G= ENSP00000505877.1:n.*406G=
ENST00000681278.1:n.1108G=
ENST00000681289.1:n.4746G=
ENST00000681361.1:c.*418G= ENSP00000506679.1:n.*418G=
ENST00000681430.1:c.751G= ENSP00000506301.1:p.Val251=
ENST00000681446.1:c.*333G= ENSP00000506244.1:n.*333G=
ENST00000681450.1:c.*422G= ENSP00000505660.1:n.*422G=
ENST00000681548.1:c.*337G= ENSP00000505275.1:n.*337G=
ENST00000681616.1:c.*410G= ENSP00000505111.1:n.*410G=
ENST00000681621.1:c.*335G= ENSP00000505770.1:n.*335G=
ENST00000681680.1:n.2846G=
ENST00000681720.1:c.*206G= ENSP00000505438.1:n.*206G=
ENST00000681730.1:n.973G=
ENST00000681790.1:c.493G= ENSP00000505130.1:p.Val165=
ENST00000681837.1:n.1367G=
ENST00000681913.1:n.2875G=
ENST00000681916.1:c.*519G= ENSP00000506477.1:n.*519G=
ENST00000681930.1:n.2875G=
ENST00000370834.9:c.850G= ENSP00000359871.5:p.Val284=
ENST00000370841.8:c.751G= ENSP00000359878.4:p.Val251=
ENST00000420607.6:c.763G= ENSP00000409612.2:p.Val255=
ENST00000525808.5:c.*337G= ENSP00000434823.1:n.*337G=
ENST00000526129.5:c.*535G= ENSP00000434092.1:n.*535G=
ENST00000526196.5:c.*519G= ENSP00000431953.1:n.*519G=
ENST00000526930.1:n.524G=
ENST00000529059.5:n.660G=
ENST00000530953.6:c.*248G= ENSP00000431372.1:n.*248G=
ENST00000532207.5:n.481G=
ENST00000532509.5:c.*515G= ENSP00000432522.1:n.*515G=
ENST00000534334.5:c.*335G= ENSP00000435584.1:n.*335G=
ENST00000541113.5:c.643G= ENSP00000442324.1:p.Val215=
NM_000016.5:c.751G= NP_000007.1:p.Val251=
NM_001127328.2:c.763G= NP_001120800.1:p.Val255=
NM_001286042.1:c.643G= NP_001272971.1:p.Val215=
NM_001286043.1:c.850G= NP_001272972.1:p.Val284=
NM_001286044.1:c.184G= NP_001272973.1:p.Val62=
NM_000016.6:c.751G= MANE Select NP_000007.1:p.Val251=
NM_001127328.3:c.763G= NP_001120800.1:p.Val255=
NM_001286042.2:c.643G= NP_001272971.1:p.Val215=
NM_001286043.2:c.850G= NP_001272972.1:p.Val284=
NM_001286044.2:c.184G= NP_001272973.1:p.Val62=