Canonical Allele Identifier: CA1143947099
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745822C= , CM000663.2:g.75745822C= GRCh38
NC_000001.10:g.76211507C= , CM000663.1:g.76211507C= GRCh37
NC_000001.9:g.75984095C= NCBI36
NG_007045.2:g.26465C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.616C= MANE Select ENSP00000359878.5:p.Arg206=
ENST00000473018.3:n.2740C=
ENST00000532207.6:n.1505C=
ENST00000541113.6:c.616C= ENSP00000442324.2:p.Arg206=
ENST00000679509.1:n.1578C=
ENST00000679530.1:c.*384C= ENSP00000506454.1:n.*384C=
ENST00000679615.1:n.2724-3597C=
ENST00000679687.1:c.178C= ENSP00000506598.1:p.Arg60=
ENST00000679704.1:c.*382C= ENSP00000505117.1:n.*382C=
ENST00000679709.1:c.*579C= ENSP00000506623.1:n.*579C=
ENST00000679976.1:c.*200C= ENSP00000505565.1:n.*200C=
ENST00000680166.1:n.3905C=
ENST00000680517.1:c.*97-3597C= ENSP00000505803.1:n.*97-3597C=
ENST00000680582.1:n.1578C=
ENST00000680613.1:c.600-13C= ENSP00000506114.1:n.600-13C=
ENST00000680662.1:c.*530C= ENSP00000505080.1:n.*530C=
ENST00000680691.1:c.*279C= ENSP00000506487.1:n.*279C=
ENST00000680694.1:c.*204C= ENSP00000505658.1:n.*204C=
ENST00000680743.1:c.*283C= ENSP00000505073.1:n.*283C=
ENST00000680749.1:c.600-3597C= ENSP00000505122.1:n.600-3597C=
ENST00000680798.1:c.*184-3597C= ENSP00000505670.1:n.*184-3597C=
ENST00000680805.1:c.616C= ENSP00000505447.1:p.Arg206=
ENST00000680844.1:c.*400C= ENSP00000506541.1:n.*400C=
ENST00000680948.1:c.*483C= ENSP00000505441.1:n.*483C=
ENST00000680964.1:c.616C= ENSP00000505961.1:p.Arg206=
ENST00000681037.1:c.*2113-13C= ENSP00000506025.1:n.*2113-13C=
ENST00000681063.1:c.600-4629C= ENSP00000506616.1:n.600-4629C=
ENST00000681209.1:c.*364-3597C= ENSP00000505877.1:n.*364-3597C=
ENST00000681278.1:n.973C=
ENST00000681289.1:n.4611C=
ENST00000681361.1:c.*283C= ENSP00000506679.1:n.*283C=
ENST00000681430.1:c.616C= ENSP00000506301.1:p.Arg206=
ENST00000681446.1:c.*198C= ENSP00000506244.1:n.*198C=
ENST00000681450.1:c.*287C= ENSP00000505660.1:n.*287C=
ENST00000681548.1:c.*202C= ENSP00000505275.1:n.*202C=
ENST00000681616.1:c.*368-3597C= ENSP00000505111.1:n.*368-3597C=
ENST00000681621.1:c.*200C= ENSP00000505770.1:n.*200C=
ENST00000681680.1:n.2724-13C=
ENST00000681720.1:c.*71C= ENSP00000505438.1:n.*71C=
ENST00000681730.1:n.838C=
ENST00000681790.1:c.358C= ENSP00000505130.1:p.Arg120=
ENST00000681837.1:n.1232C=
ENST00000681913.1:n.2740C=
ENST00000681916.1:c.*384C= ENSP00000506477.1:n.*384C=
ENST00000681930.1:n.2740C=
ENST00000370834.9:c.715C= ENSP00000359871.5:p.Arg239=
ENST00000370841.8:c.616C= ENSP00000359878.4:p.Arg206=
ENST00000420607.6:c.628C= ENSP00000409612.2:p.Arg210=
ENST00000525808.5:c.*202C= ENSP00000434823.1:n.*202C=
ENST00000526129.5:c.*400C= ENSP00000434092.1:n.*400C=
ENST00000526196.5:c.*384C= ENSP00000431953.1:n.*384C=
ENST00000526930.1:n.389C=
ENST00000529059.5:n.525C=
ENST00000530953.6:c.*113C= ENSP00000431372.1:n.*113C=
ENST00000532207.5:n.346C=
ENST00000532509.5:c.*380C= ENSP00000432522.1:n.*380C=
ENST00000534334.5:c.*200C= ENSP00000435584.1:n.*200C=
ENST00000541113.5:c.508C= ENSP00000442324.1:p.Arg170=
NM_000016.5:c.616C= NP_000007.1:p.Arg206=
NM_001127328.2:c.628C= NP_001120800.1:p.Arg210=
NM_001286042.1:c.508C= NP_001272971.1:p.Arg170=
NM_001286043.1:c.715C= NP_001272972.1:p.Arg239=
NM_001286044.1:c.49C= NP_001272973.1:p.Arg17=
NM_000016.6:c.616C= MANE Select NP_000007.1:p.Arg206=
NM_001127328.3:c.628C= NP_001120800.1:p.Arg210=
NM_001286042.2:c.508C= NP_001272971.1:p.Arg170=
NM_001286043.2:c.715C= NP_001272972.1:p.Arg239=
NM_001286044.2:c.49C= NP_001272973.1:p.Arg17=