Canonical Allele Identifier: CA1141056593
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761375G= , CM000663.2:g.75761375G= GRCh38
NC_000001.10:g.76227060G= , CM000663.1:g.76227060G= GRCh37
NC_000001.9:g.75999648G= NCBI36
NG_007045.2:g.42018G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1194+5G= MANE Select ENSP00000359878.5:n.1194+5G=
ENST00000473018.3:n.3318+5G=
ENST00000532207.6:n.2210G=
ENST00000541113.6:c.1098+5G= ENSP00000442324.2:n.1098+5G=
ENST00000679509.1:n.2161G=
ENST00000679530.1:c.*962+5G= ENSP00000506454.1:n.*962+5G=
ENST00000679615.1:n.3214G=
ENST00000679687.1:c.756+5G= ENSP00000506598.1:n.756+5G=
ENST00000679704.1:c.*960+5G= ENSP00000505117.1:n.*960+5G=
ENST00000679709.1:c.*1157+5G= ENSP00000506623.1:n.*1157+5G=
ENST00000679976.1:c.*778+5G= ENSP00000505565.1:n.*778+5G=
ENST00000680166.1:n.4483+5G=
ENST00000680315.1:n.1082G=
ENST00000680517.1:c.*587G= ENSP00000505803.1:n.*587G=
ENST00000680582.1:n.2156+5G=
ENST00000680613.1:c.*687+5G= ENSP00000506114.1:n.*687+5G=
ENST00000680662.1:c.*1108+5G= ENSP00000505080.1:n.*1108+5G=
ENST00000680691.1:c.*857+5G= ENSP00000506487.1:n.*857+5G=
ENST00000680694.1:c.*782+5G= ENSP00000505658.1:n.*782+5G=
ENST00000680743.1:c.*983+5G= ENSP00000505073.1:n.*983+5G=
ENST00000680749.1:c.*479+5G= ENSP00000505122.1:n.*479+5G=
ENST00000680798.1:c.*674G= ENSP00000505670.1:n.*674G=
ENST00000680805.1:c.1053+5G= ENSP00000505447.1:n.1053+5G=
ENST00000680844.1:c.*983G= ENSP00000506541.1:n.*983G=
ENST00000680948.1:c.*1061+5G= ENSP00000505441.1:n.*1061+5G=
ENST00000680964.1:c.*292G= ENSP00000505961.1:n.*292G=
ENST00000681037.1:c.*2678+5G= ENSP00000506025.1:n.*2678+5G=
ENST00000681063.1:c.*463+5G= ENSP00000506616.1:n.*463+5G=
ENST00000681209.1:c.*849+5G= ENSP00000505877.1:n.*849+5G=
ENST00000681278.1:n.1896+5G=
ENST00000681289.1:n.5189+5G=
ENST00000681361.1:c.*866G= ENSP00000506679.1:n.*866G=
ENST00000681430.1:c.*287+5G= ENSP00000506301.1:n.*287+5G=
ENST00000681446.1:c.*903G= ENSP00000506244.1:n.*903G=
ENST00000681450.1:c.*865+5G= ENSP00000505660.1:n.*865+5G=
ENST00000681548.1:c.*785G= ENSP00000505275.1:n.*785G=
ENST00000681616.1:c.*858G= ENSP00000505111.1:n.*858G=
ENST00000681621.1:c.*783G= ENSP00000505770.1:n.*783G=
ENST00000681680.1:n.3294G=
ENST00000681720.1:c.*649+5G= ENSP00000505438.1:n.*649+5G=
ENST00000681730.1:n.1416+5G=
ENST00000681790.1:c.936+5G= ENSP00000505130.1:n.936+5G=
ENST00000681837.1:n.1815G=
ENST00000681913.1:n.3440+5G=
ENST00000681916.1:c.*962+5G= ENSP00000506477.1:n.*962+5G=
ENST00000681930.1:n.3323G=
ENST00000370834.9:c.1293+5G= ENSP00000359871.5:n.1293+5G=
ENST00000370841.8:c.1194+5G= ENSP00000359878.4:n.1194+5G=
ENST00000420607.6:c.1206+5G= ENSP00000409612.2:n.1206+5G=
ENST00000481374.1:n.467+5G=
ENST00000525808.5:c.*780+5G= ENSP00000434823.1:n.*780+5G=
ENST00000526129.5:c.*983G= ENSP00000434092.1:n.*983G=
ENST00000526196.5:c.*962+5G= ENSP00000431953.1:n.*962+5G=
ENST00000528016.1:c.160-7802G= ENSP00000434284.1:n.160-7802G=
ENST00000529059.5:n.1103+5G=
ENST00000541113.5:c.1086+5G= ENSP00000442324.1:n.1086+5G=
NM_000016.5:c.1194+5G= NP_000007.1:n.1194+5G=
NM_001127328.2:c.1206+5G= NP_001120800.1:n.1206+5G=
NM_001286042.1:c.1086+5G= NP_001272971.1:n.1086+5G=
NM_001286043.1:c.1293+5G= NP_001272972.1:n.1293+5G=
NM_001286044.1:c.627+5G= NP_001272973.1:n.627+5G=
NM_000016.6:c.1194+5G= MANE Select NP_000007.1:n.1194+5G=
NM_001127328.3:c.1206+5G= NP_001120800.1:n.1206+5G=
NM_001286042.2:c.1086+5G= NP_001272971.1:n.1086+5G=
NM_001286043.2:c.1293+5G= NP_001272972.1:n.1293+5G=
NM_001286044.2:c.627+5G= NP_001272973.1:n.627+5G=