Canonical Allele Identifier: CA1176721867
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750484G= , CM000663.2:g.75750484G= GRCh38
NC_000001.10:g.76216169G= , CM000663.1:g.76216169G= GRCh37
NC_000001.9:g.75988757G= NCBI36
NG_007045.2:g.31127G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.883G= MANE Select ENSP00000359878.5:p.Ala295=
ENST00000473018.3:n.3007G=
ENST00000532207.6:n.1772G=
ENST00000541113.6:c.849+925G= ENSP00000442324.2:n.849+925G=
ENST00000679509.1:n.1845G=
ENST00000679530.1:c.*651G= ENSP00000506454.1:n.*651G=
ENST00000679615.1:n.2898G=
ENST00000679687.1:c.445G= ENSP00000506598.1:p.Ala149=
ENST00000679704.1:c.*649G= ENSP00000505117.1:n.*649G=
ENST00000679709.1:c.*846G= ENSP00000506623.1:n.*846G=
ENST00000679976.1:c.*467G= ENSP00000505565.1:n.*467G=
ENST00000680166.1:n.4172G=
ENST00000680315.1:n.766G=
ENST00000680517.1:c.*271G= ENSP00000505803.1:n.*271G=
ENST00000680582.1:n.1845G=
ENST00000680613.1:c.*254G= ENSP00000506114.1:n.*254G=
ENST00000680662.1:c.*797G= ENSP00000505080.1:n.*797G=
ENST00000680691.1:c.*546G= ENSP00000506487.1:n.*546G=
ENST00000680694.1:c.*471G= ENSP00000505658.1:n.*471G=
ENST00000680743.1:c.*550G= ENSP00000505073.1:n.*550G=
ENST00000680749.1:c.*168G= ENSP00000505122.1:n.*168G=
ENST00000680798.1:c.*358G= ENSP00000505670.1:n.*358G=
ENST00000680805.1:c.742G= ENSP00000505447.1:p.Ala248=
ENST00000680844.1:c.*667G= ENSP00000506541.1:n.*667G=
ENST00000680948.1:c.*750G= ENSP00000505441.1:n.*750G=
ENST00000680964.1:c.883G= ENSP00000505961.1:p.Ala295=
ENST00000681037.1:c.*2367G= ENSP00000506025.1:n.*2367G=
ENST00000681063.1:c.*30G= ENSP00000506616.1:n.*30G=
ENST00000681209.1:c.*538G= ENSP00000505877.1:n.*538G=
ENST00000681278.1:n.1240G=
ENST00000681289.1:n.4878G=
ENST00000681361.1:c.*550G= ENSP00000506679.1:n.*550G=
ENST00000681430.1:c.883G= ENSP00000506301.1:p.Ala295=
ENST00000681446.1:c.*465G= ENSP00000506244.1:n.*465G=
ENST00000681450.1:c.*554G= ENSP00000505660.1:n.*554G=
ENST00000681548.1:c.*469G= ENSP00000505275.1:n.*469G=
ENST00000681616.1:c.*542G= ENSP00000505111.1:n.*542G=
ENST00000681621.1:c.*467G= ENSP00000505770.1:n.*467G=
ENST00000681680.1:n.2978G=
ENST00000681720.1:c.*338G= ENSP00000505438.1:n.*338G=
ENST00000681730.1:n.1105G=
ENST00000681790.1:c.625G= ENSP00000505130.1:p.Ala209=
ENST00000681837.1:n.1499G=
ENST00000681913.1:n.3007G=
ENST00000681916.1:c.*651G= ENSP00000506477.1:n.*651G=
ENST00000681930.1:n.3007G=
ENST00000370834.9:c.982G= ENSP00000359871.5:p.Ala328=
ENST00000370841.8:c.883G= ENSP00000359878.4:p.Ala295=
ENST00000420607.6:c.895G= ENSP00000409612.2:p.Ala299=
ENST00000481374.1:n.34G=
ENST00000525808.5:c.*469G= ENSP00000434823.1:n.*469G=
ENST00000526129.5:c.*667G= ENSP00000434092.1:n.*667G=
ENST00000526196.5:c.*651G= ENSP00000431953.1:n.*651G=
ENST00000528016.1:c.97G= ENSP00000434284.1:p.Ala33=
ENST00000529059.5:n.792G=
ENST00000532207.5:n.613G=
ENST00000534334.5:c.*467G= ENSP00000435584.1:n.*467G=
ENST00000541113.5:c.775G= ENSP00000442324.1:p.Ala259=
NM_000016.5:c.883G= NP_000007.1:p.Ala295=
NM_001127328.2:c.895G= NP_001120800.1:p.Ala299=
NM_001286042.1:c.775G= NP_001272971.1:p.Ala259=
NM_001286043.1:c.982G= NP_001272972.1:p.Ala328=
NM_001286044.1:c.316G= NP_001272973.1:p.Ala106=
NM_000016.6:c.883G= MANE Select NP_000007.1:p.Ala295=
NM_001127328.3:c.895G= NP_001120800.1:p.Ala299=
NM_001286042.2:c.775G= NP_001272971.1:p.Ala259=
NM_001286043.2:c.982G= NP_001272972.1:p.Ala328=
NM_001286044.2:c.316G= NP_001272973.1:p.Ala106=