Canonical Allele Identifier: CA1176721476
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749557G= , CM000663.2:g.75749557G= GRCh38
NC_000001.10:g.76215242G= , CM000663.1:g.76215242G= GRCh37
NC_000001.9:g.75987830G= NCBI36
NG_007045.2:g.30200G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.847G= MANE Select ENSP00000359878.5:p.Val283=
ENST00000473018.3:n.2971G=
ENST00000532207.6:n.1736G=
ENST00000541113.6:c.847G= ENSP00000442324.2:p.Val283=
ENST00000679509.1:n.1809G=
ENST00000679530.1:c.*615G= ENSP00000506454.1:n.*615G=
ENST00000679615.1:n.2862G=
ENST00000679687.1:c.409G= ENSP00000506598.1:p.Val137=
ENST00000679704.1:c.*613G= ENSP00000505117.1:n.*613G=
ENST00000679709.1:c.*810G= ENSP00000506623.1:n.*810G=
ENST00000679976.1:c.*431G= ENSP00000505565.1:n.*431G=
ENST00000680166.1:n.4136G=
ENST00000680517.1:c.*235G= ENSP00000505803.1:n.*235G=
ENST00000680582.1:n.1809G=
ENST00000680613.1:c.*218G= ENSP00000506114.1:n.*218G=
ENST00000680662.1:c.*761G= ENSP00000505080.1:n.*761G=
ENST00000680691.1:c.*510G= ENSP00000506487.1:n.*510G=
ENST00000680694.1:c.*435G= ENSP00000505658.1:n.*435G=
ENST00000680743.1:c.*514G= ENSP00000505073.1:n.*514G=
ENST00000680749.1:c.*132G= ENSP00000505122.1:n.*132G=
ENST00000680798.1:c.*322G= ENSP00000505670.1:n.*322G=
ENST00000680805.1:c.709-894G= ENSP00000505447.1:n.709-894G=
ENST00000680844.1:c.*631G= ENSP00000506541.1:n.*631G=
ENST00000680948.1:c.*714G= ENSP00000505441.1:n.*714G=
ENST00000680964.1:c.847G= ENSP00000505961.1:p.Val283=
ENST00000681037.1:c.*2331G= ENSP00000506025.1:n.*2331G=
ENST00000681063.1:c.600-894G= ENSP00000506616.1:n.600-894G=
ENST00000681209.1:c.*502G= ENSP00000505877.1:n.*502G=
ENST00000681278.1:n.1204G=
ENST00000681289.1:n.4842G=
ENST00000681361.1:c.*514G= ENSP00000506679.1:n.*514G=
ENST00000681430.1:c.847G= ENSP00000506301.1:p.Val283=
ENST00000681446.1:c.*429G= ENSP00000506244.1:n.*429G=
ENST00000681450.1:c.*518G= ENSP00000505660.1:n.*518G=
ENST00000681548.1:c.*433G= ENSP00000505275.1:n.*433G=
ENST00000681616.1:c.*506G= ENSP00000505111.1:n.*506G=
ENST00000681621.1:c.*431G= ENSP00000505770.1:n.*431G=
ENST00000681680.1:n.2942G=
ENST00000681720.1:c.*302G= ENSP00000505438.1:n.*302G=
ENST00000681730.1:n.1069G=
ENST00000681790.1:c.589G= ENSP00000505130.1:p.Val197=
ENST00000681837.1:n.1463G=
ENST00000681913.1:n.2971G=
ENST00000681916.1:c.*615G= ENSP00000506477.1:n.*615G=
ENST00000681930.1:n.2971G=
ENST00000370834.9:c.946G= ENSP00000359871.5:p.Val316=
ENST00000370841.8:c.847G= ENSP00000359878.4:p.Val283=
ENST00000420607.6:c.859G= ENSP00000409612.2:p.Val287=
ENST00000525808.5:c.*433G= ENSP00000434823.1:n.*433G=
ENST00000526129.5:c.*631G= ENSP00000434092.1:n.*631G=
ENST00000526196.5:c.*615G= ENSP00000431953.1:n.*615G=
ENST00000528016.1:c.61G= ENSP00000434284.1:p.Val21=
ENST00000529059.5:n.756G=
ENST00000532207.5:n.577G=
ENST00000534334.5:c.*431G= ENSP00000435584.1:n.*431G=
ENST00000541113.5:c.739G= ENSP00000442324.1:p.Val247=
NM_000016.5:c.847G= NP_000007.1:p.Val283=
NM_001127328.2:c.859G= NP_001120800.1:p.Val287=
NM_001286042.1:c.739G= NP_001272971.1:p.Val247=
NM_001286043.1:c.946G= NP_001272972.1:p.Val316=
NM_001286044.1:c.280G= NP_001272973.1:p.Val94=
NM_000016.6:c.847G= MANE Select NP_000007.1:p.Val283=
NM_001127328.3:c.859G= NP_001120800.1:p.Val287=
NM_001286042.2:c.739G= NP_001272971.1:p.Val247=
NM_001286043.2:c.946G= NP_001272972.1:p.Val316=
NM_001286044.2:c.280G= NP_001272973.1:p.Val94=