Canonical Allele Identifier: CA1003303777
Gene: ACADM HGNC NCBI

Linked Data

dbSNP Id: rs1648850642

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761410dup , CM000663.2:g.75761410dup GRCh38
NC_000001.10:g.76227095dup , CM000663.1:g.76227095dup GRCh37
NC_000001.9:g.75999683dup NCBI36
NG_007045.2:g.42053dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1194+40dup MANE Select ENSP00000359878.5:n.1194+40dup
ENST00000473018.3:n.3318+40dup
ENST00000532207.6:n.2245dup
ENST00000541113.6:c.1098+40dup ENSP00000442324.2:n.1098+40dup
ENST00000679509.1:n.2196dup
ENST00000679530.1:c.*962+40dup ENSP00000506454.1:n.*962+40dup
ENST00000679615.1:n.3249dup
ENST00000679687.1:c.756+40dup ENSP00000506598.1:n.756+40dup
ENST00000679704.1:c.*960+40dup ENSP00000505117.1:n.*960+40dup
ENST00000679709.1:c.*1157+40dup ENSP00000506623.1:n.*1157+40dup
ENST00000679976.1:c.*778+40dup ENSP00000505565.1:n.*778+40dup
ENST00000680166.1:n.4483+40dup
ENST00000680315.1:n.1117dup
ENST00000680517.1:c.*622dup ENSP00000505803.1:n.*622dup
ENST00000680582.1:n.2156+40dup
ENST00000680613.1:c.*687+40dup ENSP00000506114.1:n.*687+40dup
ENST00000680662.1:c.*1108+40dup ENSP00000505080.1:n.*1108+40dup
ENST00000680691.1:c.*857+40dup ENSP00000506487.1:n.*857+40dup
ENST00000680694.1:c.*782+40dup ENSP00000505658.1:n.*782+40dup
ENST00000680743.1:c.*983+40dup ENSP00000505073.1:n.*983+40dup
ENST00000680749.1:c.*479+40dup ENSP00000505122.1:n.*479+40dup
ENST00000680798.1:c.*709dup ENSP00000505670.1:n.*709dup
ENST00000680805.1:c.1053+40dup ENSP00000505447.1:n.1053+40dup
ENST00000680844.1:c.*1018dup ENSP00000506541.1:n.*1018dup
ENST00000680948.1:c.*1061+40dup ENSP00000505441.1:n.*1061+40dup
ENST00000680964.1:c.*327dup ENSP00000505961.1:n.*327dup
ENST00000681037.1:c.*2678+40dup ENSP00000506025.1:n.*2678+40dup
ENST00000681063.1:c.*463+40dup ENSP00000506616.1:n.*463+40dup
ENST00000681209.1:c.*849+40dup ENSP00000505877.1:n.*849+40dup
ENST00000681278.1:n.1896+40dup
ENST00000681289.1:n.5189+40dup
ENST00000681361.1:c.*901dup ENSP00000506679.1:n.*901dup
ENST00000681430.1:c.*287+40dup ENSP00000506301.1:n.*287+40dup
ENST00000681446.1:c.*938dup ENSP00000506244.1:n.*938dup
ENST00000681450.1:c.*865+40dup ENSP00000505660.1:n.*865+40dup
ENST00000681548.1:c.*820dup ENSP00000505275.1:n.*820dup
ENST00000681616.1:c.*893dup ENSP00000505111.1:n.*893dup
ENST00000681621.1:c.*818dup ENSP00000505770.1:n.*818dup
ENST00000681680.1:n.3329dup
ENST00000681720.1:c.*649+40dup ENSP00000505438.1:n.*649+40dup
ENST00000681730.1:n.1416+40dup
ENST00000681790.1:c.936+40dup ENSP00000505130.1:n.936+40dup
ENST00000681837.1:n.1850dup
ENST00000681913.1:n.3440+40dup
ENST00000681916.1:c.*962+40dup ENSP00000506477.1:n.*962+40dup
ENST00000681930.1:n.3358dup
ENST00000370834.9:c.1293+40dup ENSP00000359871.5:n.1293+40dup
ENST00000370841.8:c.1194+40dup ENSP00000359878.4:n.1194+40dup
ENST00000420607.6:c.1206+40dup ENSP00000409612.2:n.1206+40dup
ENST00000481374.1:n.467+40dup
ENST00000525808.5:c.*780+40dup ENSP00000434823.1:n.*780+40dup
ENST00000526129.5:c.*1018dup ENSP00000434092.1:n.*1018dup
ENST00000526196.5:c.*962+40dup ENSP00000431953.1:n.*962+40dup
ENST00000528016.1:c.160-7767dup ENSP00000434284.1:n.160-7767dup
ENST00000529059.5:n.1103+40dup
ENST00000541113.5:c.1086+40dup ENSP00000442324.1:n.1086+40dup
NM_000016.5:c.1194+40dup NP_000007.1:n.1194+40dup
NM_001127328.2:c.1206+40dup NP_001120800.1:n.1206+40dup
NM_001286042.1:c.1086+40dup NP_001272971.1:n.1086+40dup
NM_001286043.1:c.1293+40dup NP_001272972.1:n.1293+40dup
NM_001286044.1:c.627+40dup NP_001272973.1:n.627+40dup
NM_000016.6:c.1194+40dup MANE Select NP_000007.1:n.1194+40dup
NM_001127328.3:c.1206+40dup NP_001120800.1:n.1206+40dup
NM_001286042.2:c.1086+40dup NP_001272971.1:n.1086+40dup
NM_001286043.2:c.1293+40dup NP_001272972.1:n.1293+40dup
NM_001286044.2:c.627+40dup NP_001272973.1:n.627+40dup