Canonical Allele Identifier: CA1176721434
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749427C= , CM000663.2:g.75749427C= GRCh38
NC_000001.10:g.76215112C= , CM000663.1:g.76215112C= GRCh37
NC_000001.9:g.75987700C= NCBI36
NG_007045.2:g.30070C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.717C= MANE Select ENSP00000359878.5:p.Asn239=
ENST00000473018.3:n.2841C=
ENST00000532207.6:n.1606C=
ENST00000541113.6:c.717C= ENSP00000442324.2:p.Asn239=
ENST00000679509.1:n.1679C=
ENST00000679530.1:c.*485C= ENSP00000506454.1:n.*485C=
ENST00000679615.1:n.2732C=
ENST00000679687.1:c.279C= ENSP00000506598.1:p.Asn93=
ENST00000679704.1:c.*483C= ENSP00000505117.1:n.*483C=
ENST00000679709.1:c.*680C= ENSP00000506623.1:n.*680C=
ENST00000679976.1:c.*301C= ENSP00000505565.1:n.*301C=
ENST00000680166.1:n.4006C=
ENST00000680517.1:c.*105C= ENSP00000505803.1:n.*105C=
ENST00000680582.1:n.1679C=
ENST00000680613.1:c.*88C= ENSP00000506114.1:n.*88C=
ENST00000680662.1:c.*631C= ENSP00000505080.1:n.*631C=
ENST00000680691.1:c.*380C= ENSP00000506487.1:n.*380C=
ENST00000680694.1:c.*305C= ENSP00000505658.1:n.*305C=
ENST00000680743.1:c.*384C= ENSP00000505073.1:n.*384C=
ENST00000680749.1:c.*2C= ENSP00000505122.1:n.*2C=
ENST00000680798.1:c.*192C= ENSP00000505670.1:n.*192C=
ENST00000680805.1:c.709-1024C= ENSP00000505447.1:n.709-1024C=
ENST00000680844.1:c.*501C= ENSP00000506541.1:n.*501C=
ENST00000680948.1:c.*584C= ENSP00000505441.1:n.*584C=
ENST00000680964.1:c.717C= ENSP00000505961.1:p.Asn239=
ENST00000681037.1:c.*2201C= ENSP00000506025.1:n.*2201C=
ENST00000681063.1:c.600-1024C= ENSP00000506616.1:n.600-1024C=
ENST00000681209.1:c.*372C= ENSP00000505877.1:n.*372C=
ENST00000681278.1:n.1074C=
ENST00000681289.1:n.4712C=
ENST00000681361.1:c.*384C= ENSP00000506679.1:n.*384C=
ENST00000681430.1:c.717C= ENSP00000506301.1:p.Asn239=
ENST00000681446.1:c.*299C= ENSP00000506244.1:n.*299C=
ENST00000681450.1:c.*388C= ENSP00000505660.1:n.*388C=
ENST00000681548.1:c.*303C= ENSP00000505275.1:n.*303C=
ENST00000681616.1:c.*376C= ENSP00000505111.1:n.*376C=
ENST00000681621.1:c.*301C= ENSP00000505770.1:n.*301C=
ENST00000681680.1:n.2812C=
ENST00000681720.1:c.*172C= ENSP00000505438.1:n.*172C=
ENST00000681730.1:n.939C=
ENST00000681790.1:c.459C= ENSP00000505130.1:p.Asn153=
ENST00000681837.1:n.1333C=
ENST00000681913.1:n.2841C=
ENST00000681916.1:c.*485C= ENSP00000506477.1:n.*485C=
ENST00000681930.1:n.2841C=
ENST00000370834.9:c.816C= ENSP00000359871.5:p.Asn272=
ENST00000370841.8:c.717C= ENSP00000359878.4:p.Asn239=
ENST00000420607.6:c.729C= ENSP00000409612.2:p.Asn243=
ENST00000525808.5:c.*303C= ENSP00000434823.1:n.*303C=
ENST00000526129.5:c.*501C= ENSP00000434092.1:n.*501C=
ENST00000526196.5:c.*485C= ENSP00000431953.1:n.*485C=
ENST00000526930.1:n.490C=
ENST00000529059.5:n.626C=
ENST00000530953.6:c.*214C= ENSP00000431372.1:n.*214C=
ENST00000532207.5:n.447C=
ENST00000532509.5:c.*481C= ENSP00000432522.1:n.*481C=
ENST00000534334.5:c.*301C= ENSP00000435584.1:n.*301C=
ENST00000541113.5:c.609C= ENSP00000442324.1:p.Asn203=
NM_000016.5:c.717C= NP_000007.1:p.Asn239=
NM_001127328.2:c.729C= NP_001120800.1:p.Asn243=
NM_001286042.1:c.609C= NP_001272971.1:p.Asn203=
NM_001286043.1:c.816C= NP_001272972.1:p.Asn272=
NM_001286044.1:c.150C= NP_001272973.1:p.Asn50=
NM_000016.6:c.717C= MANE Select NP_000007.1:p.Asn239=
NM_001127328.3:c.729C= NP_001120800.1:p.Asn243=
NM_001286042.2:c.609C= NP_001272971.1:p.Asn203=
NM_001286043.2:c.816C= NP_001272972.1:p.Asn272=
NM_001286044.2:c.150C= NP_001272973.1:p.Asn50=