Canonical Allele Identifier: CA1149136484
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749466C= , CM000663.2:g.75749466C= GRCh38
NC_000001.10:g.76215151C= , CM000663.1:g.76215151C= GRCh37
NC_000001.9:g.75987739C= NCBI36
NG_007045.2:g.30109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.756C= MANE Select ENSP00000359878.5:p.Phe252=
ENST00000473018.3:n.2880C=
ENST00000532207.6:n.1645C=
ENST00000541113.6:c.756C= ENSP00000442324.2:p.Phe252=
ENST00000679509.1:n.1718C=
ENST00000679530.1:c.*524C= ENSP00000506454.1:n.*524C=
ENST00000679615.1:n.2771C=
ENST00000679687.1:c.318C= ENSP00000506598.1:p.Phe106=
ENST00000679704.1:c.*522C= ENSP00000505117.1:n.*522C=
ENST00000679709.1:c.*719C= ENSP00000506623.1:n.*719C=
ENST00000679976.1:c.*340C= ENSP00000505565.1:n.*340C=
ENST00000680166.1:n.4045C=
ENST00000680517.1:c.*144C= ENSP00000505803.1:n.*144C=
ENST00000680582.1:n.1718C=
ENST00000680613.1:c.*127C= ENSP00000506114.1:n.*127C=
ENST00000680662.1:c.*670C= ENSP00000505080.1:n.*670C=
ENST00000680691.1:c.*419C= ENSP00000506487.1:n.*419C=
ENST00000680694.1:c.*344C= ENSP00000505658.1:n.*344C=
ENST00000680743.1:c.*423C= ENSP00000505073.1:n.*423C=
ENST00000680749.1:c.*41C= ENSP00000505122.1:n.*41C=
ENST00000680798.1:c.*231C= ENSP00000505670.1:n.*231C=
ENST00000680805.1:c.709-985C= ENSP00000505447.1:n.709-985C=
ENST00000680844.1:c.*540C= ENSP00000506541.1:n.*540C=
ENST00000680948.1:c.*623C= ENSP00000505441.1:n.*623C=
ENST00000680964.1:c.756C= ENSP00000505961.1:p.Phe252=
ENST00000681037.1:c.*2240C= ENSP00000506025.1:n.*2240C=
ENST00000681063.1:c.600-985C= ENSP00000506616.1:n.600-985C=
ENST00000681209.1:c.*411C= ENSP00000505877.1:n.*411C=
ENST00000681278.1:n.1113C=
ENST00000681289.1:n.4751C=
ENST00000681361.1:c.*423C= ENSP00000506679.1:n.*423C=
ENST00000681430.1:c.756C= ENSP00000506301.1:p.Phe252=
ENST00000681446.1:c.*338C= ENSP00000506244.1:n.*338C=
ENST00000681450.1:c.*427C= ENSP00000505660.1:n.*427C=
ENST00000681548.1:c.*342C= ENSP00000505275.1:n.*342C=
ENST00000681616.1:c.*415C= ENSP00000505111.1:n.*415C=
ENST00000681621.1:c.*340C= ENSP00000505770.1:n.*340C=
ENST00000681680.1:n.2851C=
ENST00000681720.1:c.*211C= ENSP00000505438.1:n.*211C=
ENST00000681730.1:n.978C=
ENST00000681790.1:c.498C= ENSP00000505130.1:p.Phe166=
ENST00000681837.1:n.1372C=
ENST00000681913.1:n.2880C=
ENST00000681916.1:c.*524C= ENSP00000506477.1:n.*524C=
ENST00000681930.1:n.2880C=
ENST00000370834.9:c.855C= ENSP00000359871.5:p.Phe285=
ENST00000370841.8:c.756C= ENSP00000359878.4:p.Phe252=
ENST00000420607.6:c.768C= ENSP00000409612.2:p.Phe256=
ENST00000525808.5:c.*342C= ENSP00000434823.1:n.*342C=
ENST00000526129.5:c.*540C= ENSP00000434092.1:n.*540C=
ENST00000526196.5:c.*524C= ENSP00000431953.1:n.*524C=
ENST00000526930.1:n.529C=
ENST00000529059.5:n.665C=
ENST00000530953.6:c.*253C= ENSP00000431372.1:n.*253C=
ENST00000532207.5:n.486C=
ENST00000532509.5:c.*520C= ENSP00000432522.1:n.*520C=
ENST00000534334.5:c.*340C= ENSP00000435584.1:n.*340C=
ENST00000541113.5:c.648C= ENSP00000442324.1:p.Phe216=
NM_000016.5:c.756C= NP_000007.1:p.Phe252=
NM_001127328.2:c.768C= NP_001120800.1:p.Phe256=
NM_001286042.1:c.648C= NP_001272971.1:p.Phe216=
NM_001286043.1:c.855C= NP_001272972.1:p.Phe285=
NM_001286044.1:c.189C= NP_001272973.1:p.Phe63=
NM_000016.6:c.756C= MANE Select NP_000007.1:p.Phe252=
NM_001127328.3:c.768C= NP_001120800.1:p.Phe256=
NM_001286042.2:c.648C= NP_001272971.1:p.Phe216=
NM_001286043.2:c.855C= NP_001272972.1:p.Phe285=
NM_001286044.2:c.189C= NP_001272973.1:p.Phe63=