Canonical Allele Identifier: CA1176715779
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740085A= , CM000663.2:g.75740085A= GRCh38
NC_000001.10:g.76205770A= , CM000663.1:g.76205770A= GRCh37
NC_000001.9:g.75978358A= NCBI36
NG_007045.2:g.20728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.574A= MANE Select ENSP00000359878.5:p.Ile192=
ENST00000473018.3:n.2698A=
ENST00000541113.6:c.574A= ENSP00000442324.2:p.Ile192=
ENST00000679509.1:n.1536A=
ENST00000679530.1:c.*342A= ENSP00000506454.1:n.*342A=
ENST00000679615.1:n.2698A=
ENST00000679687.1:c.136A= ENSP00000506598.1:p.Ile46=
ENST00000679704.1:c.*340A= ENSP00000505117.1:n.*340A=
ENST00000679709.1:c.*537A= ENSP00000506623.1:n.*537A=
ENST00000679804.1:n.313A=
ENST00000679976.1:c.*158A= ENSP00000505565.1:n.*158A=
ENST00000680166.1:n.3863A=
ENST00000680517.1:c.*71A= ENSP00000505803.1:n.*71A=
ENST00000680582.1:n.1536A=
ENST00000680613.1:c.574A= ENSP00000506114.1:p.Ile192=
ENST00000680662.1:c.*488A= ENSP00000505080.1:n.*488A=
ENST00000680691.1:c.*237A= ENSP00000506487.1:n.*237A=
ENST00000680694.1:c.*162A= ENSP00000505658.1:n.*162A=
ENST00000680743.1:c.*241A= ENSP00000505073.1:n.*241A=
ENST00000680749.1:c.574A= ENSP00000505122.1:p.Ile192=
ENST00000680798.1:c.*158A= ENSP00000505670.1:n.*158A=
ENST00000680805.1:c.574A= ENSP00000505447.1:p.Ile192=
ENST00000680844.1:c.*358A= ENSP00000506541.1:n.*358A=
ENST00000680948.1:c.*441A= ENSP00000505441.1:n.*441A=
ENST00000680964.1:c.574A= ENSP00000505961.1:p.Ile192=
ENST00000681037.1:c.574A= ENSP00000506025.1:p.Ile192=
ENST00000681063.1:c.574A= ENSP00000506616.1:p.Ile192=
ENST00000681209.1:c.*338A= ENSP00000505877.1:n.*338A=
ENST00000681278.1:n.931A=
ENST00000681289.1:n.931A=
ENST00000681361.1:c.*241A= ENSP00000506679.1:n.*241A=
ENST00000681430.1:c.574A= ENSP00000506301.1:p.Ile192=
ENST00000681446.1:c.*156A= ENSP00000506244.1:n.*156A=
ENST00000681450.1:c.*245A= ENSP00000505660.1:n.*245A=
ENST00000681548.1:c.*160A= ENSP00000505275.1:n.*160A=
ENST00000681616.1:c.*342A= ENSP00000505111.1:n.*342A=
ENST00000681621.1:c.*158A= ENSP00000505770.1:n.*158A=
ENST00000681680.1:n.2698A=
ENST00000681720.1:c.*55-5721A= ENSP00000505438.1:n.*55-5721A=
ENST00000681730.1:n.796A=
ENST00000681790.1:c.316A= ENSP00000505130.1:p.Ile106=
ENST00000681837.1:n.1190A=
ENST00000681913.1:n.2698A=
ENST00000681916.1:c.*342A= ENSP00000506477.1:n.*342A=
ENST00000681930.1:n.2698A=
ENST00000370834.9:c.673A= ENSP00000359871.5:p.Ile225=
ENST00000370841.8:c.574A= ENSP00000359878.4:p.Ile192=
ENST00000420607.6:c.586A= ENSP00000409612.2:p.Ile196=
ENST00000525808.5:c.*160A= ENSP00000434823.1:n.*160A=
ENST00000526129.5:c.*358A= ENSP00000434092.1:n.*358A=
ENST00000526196.5:c.*342A= ENSP00000431953.1:n.*342A=
ENST00000526930.1:n.347A=
ENST00000529059.5:n.483A=
ENST00000530953.6:c.*71A= ENSP00000431372.1:n.*71A=
ENST00000532509.5:c.*338A= ENSP00000432522.1:n.*338A=
ENST00000534334.5:c.*158A= ENSP00000435584.1:n.*158A=
ENST00000541113.5:c.466A= ENSP00000442324.1:p.Ile156=
NM_000016.5:c.574A= NP_000007.1:p.Ile192=
NM_001127328.2:c.586A= NP_001120800.1:p.Ile196=
NM_001286042.1:c.466A= NP_001272971.1:p.Ile156=
NM_001286043.1:c.673A= NP_001272972.1:p.Ile225=
NM_001286044.1:c.7A= NP_001272973.1:p.Ile3=
NM_000016.6:c.574A= MANE Select NP_000007.1:p.Ile192=
NM_001127328.3:c.586A= NP_001120800.1:p.Ile196=
NM_001286042.2:c.466A= NP_001272971.1:p.Ile156=
NM_001286043.2:c.673A= NP_001272972.1:p.Ile225=
NM_001286044.2:c.7A= NP_001272973.1:p.Ile3=