Canonical Allele Identifier: CA2586966782
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761367del , CM000663.2:g.75761367del GRCh38
NC_000001.10:g.76227052del , CM000663.1:g.76227052del GRCh37
NC_000001.9:g.75999640del NCBI36
NG_007045.2:g.42010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1191del MANE Select ENSP00000359878.5:p.Gln398ArgfsTer14
ENST00000473018.3:n.3315del
ENST00000532207.6:n.2202del
ENST00000541113.6:c.1095del ENSP00000442324.2:p.Gln366ArgfsTer14
ENST00000679509.1:n.2153del
ENST00000679530.1:c.*959del ENSP00000506454.1:n.*959del
ENST00000679615.1:n.3206del
ENST00000679687.1:c.753del ENSP00000506598.1:p.Gln252ArgfsTer14
ENST00000679704.1:c.*957del ENSP00000505117.1:n.*957del
ENST00000679709.1:c.*1154del ENSP00000506623.1:n.*1154del
ENST00000679976.1:c.*775del ENSP00000505565.1:n.*775del
ENST00000680166.1:n.4480del
ENST00000680315.1:n.1074del
ENST00000680517.1:c.*579del ENSP00000505803.1:n.*579del
ENST00000680582.1:n.2153del
ENST00000680613.1:c.*684del ENSP00000506114.1:n.*684del
ENST00000680662.1:c.*1105del ENSP00000505080.1:n.*1105del
ENST00000680691.1:c.*854del ENSP00000506487.1:n.*854del
ENST00000680694.1:c.*779del ENSP00000505658.1:n.*779del
ENST00000680743.1:c.*980del ENSP00000505073.1:n.*980del
ENST00000680749.1:c.*476del ENSP00000505122.1:n.*476del
ENST00000680798.1:c.*666del ENSP00000505670.1:n.*666del
ENST00000680805.1:c.1050del ENSP00000505447.1:p.Gln351ArgfsTer14
ENST00000680844.1:c.*975del ENSP00000506541.1:n.*975del
ENST00000680948.1:c.*1058del ENSP00000505441.1:n.*1058del
ENST00000680964.1:c.*284del ENSP00000505961.1:n.*284del
ENST00000681037.1:c.*2675del ENSP00000506025.1:n.*2675del
ENST00000681063.1:c.*460del ENSP00000506616.1:n.*460del
ENST00000681209.1:c.*846del ENSP00000505877.1:n.*846del
ENST00000681278.1:n.1893del
ENST00000681289.1:n.5186del
ENST00000681361.1:c.*858del ENSP00000506679.1:n.*858del
ENST00000681430.1:c.*284del ENSP00000506301.1:n.*284del
ENST00000681446.1:c.*895del ENSP00000506244.1:n.*895del
ENST00000681450.1:c.*862del ENSP00000505660.1:n.*862del
ENST00000681548.1:c.*777del ENSP00000505275.1:n.*777del
ENST00000681616.1:c.*850del ENSP00000505111.1:n.*850del
ENST00000681621.1:c.*775del ENSP00000505770.1:n.*775del
ENST00000681680.1:n.3286del
ENST00000681720.1:c.*646del ENSP00000505438.1:n.*646del
ENST00000681730.1:n.1413del
ENST00000681790.1:c.933del ENSP00000505130.1:p.Gln312ArgfsTer14
ENST00000681837.1:n.1807del
ENST00000681913.1:n.3437del
ENST00000681916.1:c.*959del ENSP00000506477.1:n.*959del
ENST00000681930.1:n.3315del
ENST00000370834.9:c.1290del ENSP00000359871.5:p.Gln431ArgfsTer14
ENST00000370841.8:c.1191del ENSP00000359878.4:p.Gln398ArgfsTer14
ENST00000420607.6:c.1203del ENSP00000409612.2:p.Gln402ArgfsTer14
ENST00000481374.1:n.464del
ENST00000525808.5:c.*777del ENSP00000434823.1:n.*777del
ENST00000526129.5:c.*975del ENSP00000434092.1:n.*975del
ENST00000526196.5:c.*959del ENSP00000431953.1:n.*959del
ENST00000528016.1:c.160-7810del ENSP00000434284.1:n.160-7810del
ENST00000529059.5:n.1100del
ENST00000541113.5:c.1083del ENSP00000442324.1:p.Gln362ArgfsTer14
NM_000016.5:c.1191del NP_000007.1:p.Gln398ArgfsTer14
NM_001127328.2:c.1203del NP_001120800.1:p.Gln402ArgfsTer14
NM_001286042.1:c.1083del NP_001272971.1:p.Gln362ArgfsTer14
NM_001286043.1:c.1290del NP_001272972.1:p.Gln431ArgfsTer14
NM_001286044.1:c.624del NP_001272973.1:p.Gln209ArgfsTer14
NM_000016.6:c.1191del MANE Select NP_000007.1:p.Gln398ArgfsTer14
NM_001127328.3:c.1203del NP_001120800.1:p.Gln402ArgfsTer14
NM_001286042.2:c.1083del NP_001272971.1:p.Gln362ArgfsTer14
NM_001286043.2:c.1290del NP_001272972.1:p.Gln431ArgfsTer14
NM_001286044.2:c.624del NP_001272973.1:p.Gln209ArgfsTer14