Canonical Allele Identifier: CA1176726798
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761125C= , CM000663.2:g.75761125C= GRCh38
NC_000001.10:g.76226810C= , CM000663.1:g.76226810C= GRCh37
NC_000001.9:g.75999398C= NCBI36
NG_007045.2:g.41768C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.949C= MANE Select ENSP00000359878.5:p.Gln317=
ENST00000473018.3:n.3073C=
ENST00000532207.6:n.1960C=
ENST00000541113.6:c.853C= ENSP00000442324.2:p.Gln285=
ENST00000679509.1:n.1911C=
ENST00000679530.1:c.*717C= ENSP00000506454.1:n.*717C=
ENST00000679615.1:n.2964C=
ENST00000679687.1:c.511C= ENSP00000506598.1:p.Gln171=
ENST00000679704.1:c.*715C= ENSP00000505117.1:n.*715C=
ENST00000679709.1:c.*912C= ENSP00000506623.1:n.*912C=
ENST00000679976.1:c.*533C= ENSP00000505565.1:n.*533C=
ENST00000680166.1:n.4238C=
ENST00000680315.1:n.832C=
ENST00000680517.1:c.*337C= ENSP00000505803.1:n.*337C=
ENST00000680582.1:n.1911C=
ENST00000680613.1:c.*442C= ENSP00000506114.1:n.*442C=
ENST00000680662.1:c.*863C= ENSP00000505080.1:n.*863C=
ENST00000680691.1:c.*612C= ENSP00000506487.1:n.*612C=
ENST00000680694.1:c.*537C= ENSP00000505658.1:n.*537C=
ENST00000680743.1:c.*738C= ENSP00000505073.1:n.*738C=
ENST00000680749.1:c.*234C= ENSP00000505122.1:n.*234C=
ENST00000680798.1:c.*424C= ENSP00000505670.1:n.*424C=
ENST00000680805.1:c.808C= ENSP00000505447.1:p.Gln270=
ENST00000680844.1:c.*733C= ENSP00000506541.1:n.*733C=
ENST00000680948.1:c.*816C= ENSP00000505441.1:n.*816C=
ENST00000680964.1:c.*42C= ENSP00000505961.1:n.*42C=
ENST00000681037.1:c.*2433C= ENSP00000506025.1:n.*2433C=
ENST00000681063.1:c.*218C= ENSP00000506616.1:n.*218C=
ENST00000681209.1:c.*604C= ENSP00000505877.1:n.*604C=
ENST00000681278.1:n.1651C=
ENST00000681289.1:n.4944C=
ENST00000681361.1:c.*616C= ENSP00000506679.1:n.*616C=
ENST00000681430.1:c.*42C= ENSP00000506301.1:n.*42C=
ENST00000681446.1:c.*653C= ENSP00000506244.1:n.*653C=
ENST00000681450.1:c.*620C= ENSP00000505660.1:n.*620C=
ENST00000681548.1:c.*535C= ENSP00000505275.1:n.*535C=
ENST00000681616.1:c.*608C= ENSP00000505111.1:n.*608C=
ENST00000681621.1:c.*533C= ENSP00000505770.1:n.*533C=
ENST00000681680.1:n.3044C=
ENST00000681720.1:c.*404C= ENSP00000505438.1:n.*404C=
ENST00000681730.1:n.1171C=
ENST00000681790.1:c.691C= ENSP00000505130.1:p.Gln231=
ENST00000681837.1:n.1565C=
ENST00000681913.1:n.3195C=
ENST00000681916.1:c.*717C= ENSP00000506477.1:n.*717C=
ENST00000681930.1:n.3073C=
ENST00000370834.9:c.1048C= ENSP00000359871.5:p.Gln350=
ENST00000370841.8:c.949C= ENSP00000359878.4:p.Gln317=
ENST00000420607.6:c.961C= ENSP00000409612.2:p.Gln321=
ENST00000481374.1:n.222C=
ENST00000525808.5:c.*535C= ENSP00000434823.1:n.*535C=
ENST00000526129.5:c.*733C= ENSP00000434092.1:n.*733C=
ENST00000526196.5:c.*717C= ENSP00000431953.1:n.*717C=
ENST00000528016.1:c.160-8052C= ENSP00000434284.1:n.160-8052C=
ENST00000529059.5:n.858C=
ENST00000532207.5:n.679C=
ENST00000534334.5:c.*690C= ENSP00000435584.1:n.*690C=
ENST00000541113.5:c.841C= ENSP00000442324.1:p.Gln281=
NM_000016.5:c.949C= NP_000007.1:p.Gln317=
NM_001127328.2:c.961C= NP_001120800.1:p.Gln321=
NM_001286042.1:c.841C= NP_001272971.1:p.Gln281=
NM_001286043.1:c.1048C= NP_001272972.1:p.Gln350=
NM_001286044.1:c.382C= NP_001272973.1:p.Gln128=
NM_000016.6:c.949C= MANE Select NP_000007.1:p.Gln317=
NM_001127328.3:c.961C= NP_001120800.1:p.Gln321=
NM_001286042.2:c.841C= NP_001272971.1:p.Gln281=
NM_001286043.2:c.1048C= NP_001272972.1:p.Gln350=
NM_001286044.2:c.382C= NP_001272973.1:p.Gln128=