Canonical Allele Identifier: CA340815394
Gene: ACADM HGNC NCBI

Linked Data

dbSNP Id: rs1438717698

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.574A>G MANE Select ENSP00000359878.5:p.Ile192Val
ENST00000473018.3:n.2698A>G
ENST00000541113.6:c.574A>G ENSP00000442324.2:p.Ile192Val
ENST00000679509.1:n.1536A>G
ENST00000679530.1:c.*342A>G ENSP00000506454.1:n.*342A>G
ENST00000679615.1:n.2698A>G
ENST00000679687.1:c.136A>G ENSP00000506598.1:p.Ile46Val
ENST00000679704.1:c.*340A>G ENSP00000505117.1:n.*340A>G
ENST00000679709.1:c.*537A>G ENSP00000506623.1:n.*537A>G
ENST00000679804.1:n.313A>G
ENST00000679976.1:c.*158A>G ENSP00000505565.1:n.*158A>G
ENST00000680166.1:n.3863A>G
ENST00000680517.1:c.*71A>G ENSP00000505803.1:n.*71A>G
ENST00000680582.1:n.1536A>G
ENST00000680613.1:c.574A>G ENSP00000506114.1:p.Ile192Val
ENST00000680662.1:c.*488A>G ENSP00000505080.1:n.*488A>G
ENST00000680691.1:c.*237A>G ENSP00000506487.1:n.*237A>G
ENST00000680694.1:c.*162A>G ENSP00000505658.1:n.*162A>G
ENST00000680743.1:c.*241A>G ENSP00000505073.1:n.*241A>G
ENST00000680749.1:c.574A>G ENSP00000505122.1:p.Ile192Val
ENST00000680798.1:c.*158A>G ENSP00000505670.1:n.*158A>G
ENST00000680805.1:c.574A>G ENSP00000505447.1:p.Ile192Val
ENST00000680844.1:c.*358A>G ENSP00000506541.1:n.*358A>G
ENST00000680948.1:c.*441A>G ENSP00000505441.1:n.*441A>G
ENST00000680964.1:c.574A>G ENSP00000505961.1:p.Ile192Val
ENST00000681037.1:c.574A>G ENSP00000506025.1:p.Ile192Val
ENST00000681063.1:c.574A>G ENSP00000506616.1:p.Ile192Val
ENST00000681209.1:c.*338A>G ENSP00000505877.1:n.*338A>G
ENST00000681278.1:n.931A>G
ENST00000681289.1:n.931A>G
ENST00000681361.1:c.*241A>G ENSP00000506679.1:n.*241A>G
ENST00000681430.1:c.574A>G ENSP00000506301.1:p.Ile192Val
ENST00000681446.1:c.*156A>G ENSP00000506244.1:n.*156A>G
ENST00000681450.1:c.*245A>G ENSP00000505660.1:n.*245A>G
ENST00000681548.1:c.*160A>G ENSP00000505275.1:n.*160A>G
ENST00000681616.1:c.*342A>G ENSP00000505111.1:n.*342A>G
ENST00000681621.1:c.*158A>G ENSP00000505770.1:n.*158A>G
ENST00000681680.1:n.2698A>G
ENST00000681720.1:c.*55-5721A>G ENSP00000505438.1:n.*55-5721A>G
ENST00000681730.1:n.796A>G
ENST00000681790.1:c.316A>G ENSP00000505130.1:p.Ile106Val
ENST00000681837.1:n.1190A>G
ENST00000681913.1:n.2698A>G
ENST00000681916.1:c.*342A>G ENSP00000506477.1:n.*342A>G
ENST00000681930.1:n.2698A>G
ENST00000370834.9:c.673A>G ENSP00000359871.5:p.Ile225Val
ENST00000370841.8:c.574A>G ENSP00000359878.4:p.Ile192Val
ENST00000420607.6:c.586A>G ENSP00000409612.2:p.Ile196Val
ENST00000525808.5:c.*160A>G ENSP00000434823.1:n.*160A>G
ENST00000526129.5:c.*358A>G ENSP00000434092.1:n.*358A>G
ENST00000526196.5:c.*342A>G ENSP00000431953.1:n.*342A>G
ENST00000526930.1:n.347A>G
ENST00000529059.5:n.483A>G
ENST00000530953.6:c.*71A>G ENSP00000431372.1:n.*71A>G
ENST00000532509.5:c.*338A>G ENSP00000432522.1:n.*338A>G
ENST00000534334.5:c.*158A>G ENSP00000435584.1:n.*158A>G
ENST00000541113.5:c.466A>G ENSP00000442324.1:p.Ile156Val
NM_000016.5:c.574A>G NP_000007.1:p.Ile192Val
NM_001127328.2:c.586A>G NP_001120800.1:p.Ile196Val
NM_001286042.1:c.466A>G NP_001272971.1:p.Ile156Val
NM_001286043.1:c.673A>G NP_001272972.1:p.Ile225Val
NM_001286044.1:c.7A>G NP_001272973.1:p.Ile3Val
NM_000016.6:c.574A>G MANE Select NP_000007.1:p.Ile192Val
NM_001127328.3:c.586A>G NP_001120800.1:p.Ile196Val
NM_001286042.2:c.466A>G NP_001272971.1:p.Ile156Val
NM_001286043.2:c.673A>G NP_001272972.1:p.Ile225Val
NM_001286044.2:c.7A>G NP_001272973.1:p.Ile3Val