Canonical Allele Identifier: CA1176726873
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761304T= , CM000663.2:g.75761304T= GRCh38
NC_000001.10:g.76226989T= , CM000663.1:g.76226989T= GRCh37
NC_000001.9:g.75999577T= NCBI36
NG_007045.2:g.41947T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1128T= MANE Select ENSP00000359878.5:p.Leu376=
ENST00000473018.3:n.3252T=
ENST00000532207.6:n.2139T=
ENST00000541113.6:c.1032T= ENSP00000442324.2:p.Leu344=
ENST00000679509.1:n.2090T=
ENST00000679530.1:c.*896T= ENSP00000506454.1:n.*896T=
ENST00000679615.1:n.3143T=
ENST00000679687.1:c.690T= ENSP00000506598.1:p.Leu230=
ENST00000679704.1:c.*894T= ENSP00000505117.1:n.*894T=
ENST00000679709.1:c.*1091T= ENSP00000506623.1:n.*1091T=
ENST00000679976.1:c.*712T= ENSP00000505565.1:n.*712T=
ENST00000680166.1:n.4417T=
ENST00000680315.1:n.1011T=
ENST00000680517.1:c.*516T= ENSP00000505803.1:n.*516T=
ENST00000680582.1:n.2090T=
ENST00000680613.1:c.*621T= ENSP00000506114.1:n.*621T=
ENST00000680662.1:c.*1042T= ENSP00000505080.1:n.*1042T=
ENST00000680691.1:c.*791T= ENSP00000506487.1:n.*791T=
ENST00000680694.1:c.*716T= ENSP00000505658.1:n.*716T=
ENST00000680743.1:c.*917T= ENSP00000505073.1:n.*917T=
ENST00000680749.1:c.*413T= ENSP00000505122.1:n.*413T=
ENST00000680798.1:c.*603T= ENSP00000505670.1:n.*603T=
ENST00000680805.1:c.987T= ENSP00000505447.1:p.Leu329=
ENST00000680844.1:c.*912T= ENSP00000506541.1:n.*912T=
ENST00000680948.1:c.*995T= ENSP00000505441.1:n.*995T=
ENST00000680964.1:c.*221T= ENSP00000505961.1:n.*221T=
ENST00000681037.1:c.*2612T= ENSP00000506025.1:n.*2612T=
ENST00000681063.1:c.*397T= ENSP00000506616.1:n.*397T=
ENST00000681209.1:c.*783T= ENSP00000505877.1:n.*783T=
ENST00000681278.1:n.1830T=
ENST00000681289.1:n.5123T=
ENST00000681361.1:c.*795T= ENSP00000506679.1:n.*795T=
ENST00000681430.1:c.*221T= ENSP00000506301.1:n.*221T=
ENST00000681446.1:c.*832T= ENSP00000506244.1:n.*832T=
ENST00000681450.1:c.*799T= ENSP00000505660.1:n.*799T=
ENST00000681548.1:c.*714T= ENSP00000505275.1:n.*714T=
ENST00000681616.1:c.*787T= ENSP00000505111.1:n.*787T=
ENST00000681621.1:c.*712T= ENSP00000505770.1:n.*712T=
ENST00000681680.1:n.3223T=
ENST00000681720.1:c.*583T= ENSP00000505438.1:n.*583T=
ENST00000681730.1:n.1350T=
ENST00000681790.1:c.870T= ENSP00000505130.1:p.Leu290=
ENST00000681837.1:n.1744T=
ENST00000681913.1:n.3374T=
ENST00000681916.1:c.*896T= ENSP00000506477.1:n.*896T=
ENST00000681930.1:n.3252T=
ENST00000370834.9:c.1227T= ENSP00000359871.5:p.Leu409=
ENST00000370841.8:c.1128T= ENSP00000359878.4:p.Leu376=
ENST00000420607.6:c.1140T= ENSP00000409612.2:p.Leu380=
ENST00000481374.1:n.401T=
ENST00000525808.5:c.*714T= ENSP00000434823.1:n.*714T=
ENST00000526129.5:c.*912T= ENSP00000434092.1:n.*912T=
ENST00000526196.5:c.*896T= ENSP00000431953.1:n.*896T=
ENST00000528016.1:c.160-7873T= ENSP00000434284.1:n.160-7873T=
ENST00000529059.5:n.1037T=
ENST00000541113.5:c.1020T= ENSP00000442324.1:p.Leu340=
NM_000016.5:c.1128T= NP_000007.1:p.Leu376=
NM_001127328.2:c.1140T= NP_001120800.1:p.Leu380=
NM_001286042.1:c.1020T= NP_001272971.1:p.Leu340=
NM_001286043.1:c.1227T= NP_001272972.1:p.Leu409=
NM_001286044.1:c.561T= NP_001272973.1:p.Leu187=
NM_000016.6:c.1128T= MANE Select NP_000007.1:p.Leu376=
NM_001127328.3:c.1140T= NP_001120800.1:p.Leu380=
NM_001286042.2:c.1020T= NP_001272971.1:p.Leu340=
NM_001286043.2:c.1227T= NP_001272972.1:p.Leu409=
NM_001286044.2:c.561T= NP_001272973.1:p.Leu187=