Canonical Allele Identifier: CA1176726851
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761242A= , CM000663.2:g.75761242A= GRCh38
NC_000001.10:g.76226927A= , CM000663.1:g.76226927A= GRCh37
NC_000001.9:g.75999515A= NCBI36
NG_007045.2:g.41885A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1066A= MANE Select ENSP00000359878.5:p.Ile356=
ENST00000473018.3:n.3190A=
ENST00000532207.6:n.2077A=
ENST00000541113.6:c.970A= ENSP00000442324.2:p.Ile324=
ENST00000679509.1:n.2028A=
ENST00000679530.1:c.*834A= ENSP00000506454.1:n.*834A=
ENST00000679615.1:n.3081A=
ENST00000679687.1:c.628A= ENSP00000506598.1:p.Ile210=
ENST00000679704.1:c.*832A= ENSP00000505117.1:n.*832A=
ENST00000679709.1:c.*1029A= ENSP00000506623.1:n.*1029A=
ENST00000679976.1:c.*650A= ENSP00000505565.1:n.*650A=
ENST00000680166.1:n.4355A=
ENST00000680315.1:n.949A=
ENST00000680517.1:c.*454A= ENSP00000505803.1:n.*454A=
ENST00000680582.1:n.2028A=
ENST00000680613.1:c.*559A= ENSP00000506114.1:n.*559A=
ENST00000680662.1:c.*980A= ENSP00000505080.1:n.*980A=
ENST00000680691.1:c.*729A= ENSP00000506487.1:n.*729A=
ENST00000680694.1:c.*654A= ENSP00000505658.1:n.*654A=
ENST00000680743.1:c.*855A= ENSP00000505073.1:n.*855A=
ENST00000680749.1:c.*351A= ENSP00000505122.1:n.*351A=
ENST00000680798.1:c.*541A= ENSP00000505670.1:n.*541A=
ENST00000680805.1:c.925A= ENSP00000505447.1:p.Ile309=
ENST00000680844.1:c.*850A= ENSP00000506541.1:n.*850A=
ENST00000680948.1:c.*933A= ENSP00000505441.1:n.*933A=
ENST00000680964.1:c.*159A= ENSP00000505961.1:n.*159A=
ENST00000681037.1:c.*2550A= ENSP00000506025.1:n.*2550A=
ENST00000681063.1:c.*335A= ENSP00000506616.1:n.*335A=
ENST00000681209.1:c.*721A= ENSP00000505877.1:n.*721A=
ENST00000681278.1:n.1768A=
ENST00000681289.1:n.5061A=
ENST00000681361.1:c.*733A= ENSP00000506679.1:n.*733A=
ENST00000681430.1:c.*159A= ENSP00000506301.1:n.*159A=
ENST00000681446.1:c.*770A= ENSP00000506244.1:n.*770A=
ENST00000681450.1:c.*737A= ENSP00000505660.1:n.*737A=
ENST00000681548.1:c.*652A= ENSP00000505275.1:n.*652A=
ENST00000681616.1:c.*725A= ENSP00000505111.1:n.*725A=
ENST00000681621.1:c.*650A= ENSP00000505770.1:n.*650A=
ENST00000681680.1:n.3161A=
ENST00000681720.1:c.*521A= ENSP00000505438.1:n.*521A=
ENST00000681730.1:n.1288A=
ENST00000681790.1:c.808A= ENSP00000505130.1:p.Ile270=
ENST00000681837.1:n.1682A=
ENST00000681913.1:n.3312A=
ENST00000681916.1:c.*834A= ENSP00000506477.1:n.*834A=
ENST00000681930.1:n.3190A=
ENST00000370834.9:c.1165A= ENSP00000359871.5:p.Ile389=
ENST00000370841.8:c.1066A= ENSP00000359878.4:p.Ile356=
ENST00000420607.6:c.1078A= ENSP00000409612.2:p.Ile360=
ENST00000481374.1:n.339A=
ENST00000525808.5:c.*652A= ENSP00000434823.1:n.*652A=
ENST00000526129.5:c.*850A= ENSP00000434092.1:n.*850A=
ENST00000526196.5:c.*834A= ENSP00000431953.1:n.*834A=
ENST00000528016.1:c.160-7935A= ENSP00000434284.1:n.160-7935A=
ENST00000529059.5:n.975A=
ENST00000534334.5:c.*807A= ENSP00000435584.1:n.*807A=
ENST00000541113.5:c.958A= ENSP00000442324.1:p.Ile320=
NM_000016.5:c.1066A= NP_000007.1:p.Ile356=
NM_001127328.2:c.1078A= NP_001120800.1:p.Ile360=
NM_001286042.1:c.958A= NP_001272971.1:p.Ile320=
NM_001286043.1:c.1165A= NP_001272972.1:p.Ile389=
NM_001286044.1:c.499A= NP_001272973.1:p.Ile167=
NM_000016.6:c.1066A= MANE Select NP_000007.1:p.Ile356=
NM_001127328.3:c.1078A= NP_001120800.1:p.Ile360=
NM_001286042.2:c.958A= NP_001272971.1:p.Ile320=
NM_001286043.2:c.1165A= NP_001272972.1:p.Ile389=
NM_001286044.2:c.499A= NP_001272973.1:p.Ile167=