Canonical Allele Identifier: CA1176720017
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745806G= , CM000663.2:g.75745806G= GRCh38
NC_000001.10:g.76211491G= , CM000663.1:g.76211491G= GRCh37
NC_000001.9:g.75984079G= NCBI36
NG_007045.2:g.26449G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.600G= MANE Select ENSP00000359878.5:p.Trp200=
ENST00000473018.3:n.2724G=
ENST00000532207.6:n.1489G=
ENST00000541113.6:c.600G= ENSP00000442324.2:p.Trp200=
ENST00000679509.1:n.1562G=
ENST00000679530.1:c.*368G= ENSP00000506454.1:n.*368G=
ENST00000679615.1:n.2724-3613G=
ENST00000679687.1:c.162G= ENSP00000506598.1:p.Trp54=
ENST00000679704.1:c.*366G= ENSP00000505117.1:n.*366G=
ENST00000679709.1:c.*563G= ENSP00000506623.1:n.*563G=
ENST00000679976.1:c.*184G= ENSP00000505565.1:n.*184G=
ENST00000680166.1:n.3889G=
ENST00000680517.1:c.*97-3613G= ENSP00000505803.1:n.*97-3613G=
ENST00000680582.1:n.1562G=
ENST00000680613.1:c.600-29G= ENSP00000506114.1:n.600-29G=
ENST00000680662.1:c.*514G= ENSP00000505080.1:n.*514G=
ENST00000680691.1:c.*263G= ENSP00000506487.1:n.*263G=
ENST00000680694.1:c.*188G= ENSP00000505658.1:n.*188G=
ENST00000680743.1:c.*267G= ENSP00000505073.1:n.*267G=
ENST00000680749.1:c.600-3613G= ENSP00000505122.1:n.600-3613G=
ENST00000680798.1:c.*184-3613G= ENSP00000505670.1:n.*184-3613G=
ENST00000680805.1:c.600G= ENSP00000505447.1:p.Trp200=
ENST00000680844.1:c.*384G= ENSP00000506541.1:n.*384G=
ENST00000680948.1:c.*467G= ENSP00000505441.1:n.*467G=
ENST00000680964.1:c.600G= ENSP00000505961.1:p.Trp200=
ENST00000681037.1:c.*2113-29G= ENSP00000506025.1:n.*2113-29G=
ENST00000681063.1:c.600-4645G= ENSP00000506616.1:n.600-4645G=
ENST00000681209.1:c.*364-3613G= ENSP00000505877.1:n.*364-3613G=
ENST00000681278.1:n.957G=
ENST00000681289.1:n.4595G=
ENST00000681361.1:c.*267G= ENSP00000506679.1:n.*267G=
ENST00000681430.1:c.600G= ENSP00000506301.1:p.Trp200=
ENST00000681446.1:c.*182G= ENSP00000506244.1:n.*182G=
ENST00000681450.1:c.*271G= ENSP00000505660.1:n.*271G=
ENST00000681548.1:c.*186G= ENSP00000505275.1:n.*186G=
ENST00000681616.1:c.*368-3613G= ENSP00000505111.1:n.*368-3613G=
ENST00000681621.1:c.*184G= ENSP00000505770.1:n.*184G=
ENST00000681680.1:n.2724-29G=
ENST00000681720.1:c.*55G= ENSP00000505438.1:n.*55G=
ENST00000681730.1:n.822G=
ENST00000681790.1:c.342G= ENSP00000505130.1:p.Trp114=
ENST00000681837.1:n.1216G=
ENST00000681913.1:n.2724G=
ENST00000681916.1:c.*368G= ENSP00000506477.1:n.*368G=
ENST00000681930.1:n.2724G=
ENST00000370834.9:c.699G= ENSP00000359871.5:p.Trp233=
ENST00000370841.8:c.600G= ENSP00000359878.4:p.Trp200=
ENST00000420607.6:c.612G= ENSP00000409612.2:p.Trp204=
ENST00000525808.5:c.*186G= ENSP00000434823.1:n.*186G=
ENST00000526129.5:c.*384G= ENSP00000434092.1:n.*384G=
ENST00000526196.5:c.*368G= ENSP00000431953.1:n.*368G=
ENST00000526930.1:n.373G=
ENST00000529059.5:n.509G=
ENST00000530953.6:c.*97G= ENSP00000431372.1:n.*97G=
ENST00000532207.5:n.330G=
ENST00000532509.5:c.*364G= ENSP00000432522.1:n.*364G=
ENST00000534334.5:c.*184G= ENSP00000435584.1:n.*184G=
ENST00000541113.5:c.492G= ENSP00000442324.1:p.Trp164=
NM_000016.5:c.600G= NP_000007.1:p.Trp200=
NM_001127328.2:c.612G= NP_001120800.1:p.Trp204=
NM_001286042.1:c.492G= NP_001272971.1:p.Trp164=
NM_001286043.1:c.699G= NP_001272972.1:p.Trp233=
NM_001286044.1:c.33G= NP_001272973.1:p.Trp11=
NM_000016.6:c.600G= MANE Select NP_000007.1:p.Trp200=
NM_001127328.3:c.612G= NP_001120800.1:p.Trp204=
NM_001286042.2:c.492G= NP_001272971.1:p.Trp164=
NM_001286043.2:c.699G= NP_001272972.1:p.Trp233=
NM_001286044.2:c.33G= NP_001272973.1:p.Trp11=