Canonical Allele Identifier: CA1176715777
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740083G= , CM000663.2:g.75740083G= GRCh38
NC_000001.10:g.76205768G= , CM000663.1:g.76205768G= GRCh37
NC_000001.9:g.75978356G= NCBI36
NG_007045.2:g.20726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.572G= MANE Select ENSP00000359878.5:p.Trp191=
ENST00000473018.3:n.2696G=
ENST00000541113.6:c.572G= ENSP00000442324.2:p.Trp191=
ENST00000679509.1:n.1534G=
ENST00000679530.1:c.*340G= ENSP00000506454.1:n.*340G=
ENST00000679615.1:n.2696G=
ENST00000679687.1:c.134G= ENSP00000506598.1:p.Trp45=
ENST00000679704.1:c.*338G= ENSP00000505117.1:n.*338G=
ENST00000679709.1:c.*535G= ENSP00000506623.1:n.*535G=
ENST00000679804.1:n.311G=
ENST00000679976.1:c.*156G= ENSP00000505565.1:n.*156G=
ENST00000680166.1:n.3861G=
ENST00000680517.1:c.*69G= ENSP00000505803.1:n.*69G=
ENST00000680582.1:n.1534G=
ENST00000680613.1:c.572G= ENSP00000506114.1:p.Trp191=
ENST00000680662.1:c.*486G= ENSP00000505080.1:n.*486G=
ENST00000680691.1:c.*235G= ENSP00000506487.1:n.*235G=
ENST00000680694.1:c.*160G= ENSP00000505658.1:n.*160G=
ENST00000680743.1:c.*239G= ENSP00000505073.1:n.*239G=
ENST00000680749.1:c.572G= ENSP00000505122.1:p.Trp191=
ENST00000680798.1:c.*156G= ENSP00000505670.1:n.*156G=
ENST00000680805.1:c.572G= ENSP00000505447.1:p.Trp191=
ENST00000680844.1:c.*356G= ENSP00000506541.1:n.*356G=
ENST00000680948.1:c.*439G= ENSP00000505441.1:n.*439G=
ENST00000680964.1:c.572G= ENSP00000505961.1:p.Trp191=
ENST00000681037.1:c.572G= ENSP00000506025.1:p.Trp191=
ENST00000681063.1:c.572G= ENSP00000506616.1:p.Trp191=
ENST00000681209.1:c.*336G= ENSP00000505877.1:n.*336G=
ENST00000681278.1:n.929G=
ENST00000681289.1:n.929G=
ENST00000681361.1:c.*239G= ENSP00000506679.1:n.*239G=
ENST00000681430.1:c.572G= ENSP00000506301.1:p.Trp191=
ENST00000681446.1:c.*154G= ENSP00000506244.1:n.*154G=
ENST00000681450.1:c.*243G= ENSP00000505660.1:n.*243G=
ENST00000681548.1:c.*158G= ENSP00000505275.1:n.*158G=
ENST00000681616.1:c.*340G= ENSP00000505111.1:n.*340G=
ENST00000681621.1:c.*156G= ENSP00000505770.1:n.*156G=
ENST00000681680.1:n.2696G=
ENST00000681720.1:c.*55-5723G= ENSP00000505438.1:n.*55-5723G=
ENST00000681730.1:n.794G=
ENST00000681790.1:c.314G= ENSP00000505130.1:p.Trp105=
ENST00000681837.1:n.1188G=
ENST00000681913.1:n.2696G=
ENST00000681916.1:c.*340G= ENSP00000506477.1:n.*340G=
ENST00000681930.1:n.2696G=
ENST00000370834.9:c.671G= ENSP00000359871.5:p.Trp224=
ENST00000370841.8:c.572G= ENSP00000359878.4:p.Trp191=
ENST00000420607.6:c.584G= ENSP00000409612.2:p.Trp195=
ENST00000525808.5:c.*158G= ENSP00000434823.1:n.*158G=
ENST00000526129.5:c.*356G= ENSP00000434092.1:n.*356G=
ENST00000526196.5:c.*340G= ENSP00000431953.1:n.*340G=
ENST00000526930.1:n.345G=
ENST00000529059.5:n.481G=
ENST00000530953.6:c.*69G= ENSP00000431372.1:n.*69G=
ENST00000532509.5:c.*336G= ENSP00000432522.1:n.*336G=
ENST00000534334.5:c.*156G= ENSP00000435584.1:n.*156G=
ENST00000541113.5:c.464G= ENSP00000442324.1:p.Trp155=
NM_000016.5:c.572G= NP_000007.1:p.Trp191=
NM_001127328.2:c.584G= NP_001120800.1:p.Trp195=
NM_001286042.1:c.464G= NP_001272971.1:p.Trp155=
NM_001286043.1:c.671G= NP_001272972.1:p.Trp224=
NM_001286044.1:c.5G= NP_001272973.1:p.Trp2=
NM_000016.6:c.572G= MANE Select NP_000007.1:p.Trp191=
NM_001127328.3:c.584G= NP_001120800.1:p.Trp195=
NM_001286042.2:c.464G= NP_001272971.1:p.Trp155=
NM_001286043.2:c.671G= NP_001272972.1:p.Trp224=
NM_001286044.2:c.5G= NP_001272973.1:p.Trp2=