Canonical Allele Identifier: CA2646246502
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749508_75749510del , CM000663.2:g.75749508_75749510del GRCh38
NC_000001.10:g.76215193_76215195del , CM000663.1:g.76215193_76215195del GRCh37
NC_000001.9:g.75987781_75987783del NCBI36
NG_007045.2:g.30151_30153del

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.798_800del MANE Select ENSP00000359878.5:p.Asp266_Gly267delinsGl...
ENST00000473018.3:n.2922_2924del
ENST00000532207.6:n.1687_1689del
ENST00000541113.6:c.798_800del ENSP00000442324.2:p.Asp266_Gly267delinsGl...
ENST00000679509.1:n.1760_1762del
ENST00000679530.1:c.*566_*568del ENSP00000506454.1:n.*566_*568del
ENST00000679615.1:n.2813_2815del
ENST00000679687.1:c.360_362del ENSP00000506598.1:p.Asp120_Gly121delinsGl...
ENST00000679704.1:c.*564_*566del ENSP00000505117.1:n.*564_*566del
ENST00000679709.1:c.*761_*763del ENSP00000506623.1:n.*761_*763del
ENST00000679976.1:c.*382_*384del ENSP00000505565.1:n.*382_*384del
ENST00000680166.1:n.4087_4089del
ENST00000680517.1:c.*186_*188del ENSP00000505803.1:n.*186_*188del
ENST00000680582.1:n.1760_1762del
ENST00000680613.1:c.*169_*171del ENSP00000506114.1:n.*169_*171del
ENST00000680662.1:c.*712_*714del ENSP00000505080.1:n.*712_*714del
ENST00000680691.1:c.*461_*463del ENSP00000506487.1:n.*461_*463del
ENST00000680694.1:c.*386_*388del ENSP00000505658.1:n.*386_*388del
ENST00000680743.1:c.*465_*467del ENSP00000505073.1:n.*465_*467del
ENST00000680749.1:c.*83_*85del ENSP00000505122.1:n.*83_*85del
ENST00000680798.1:c.*273_*275del ENSP00000505670.1:n.*273_*275del
ENST00000680805.1:c.709-943_709-941del ENSP00000505447.1:n.709-943_709-941del
ENST00000680844.1:c.*582_*584del ENSP00000506541.1:n.*582_*584del
ENST00000680948.1:c.*665_*667del ENSP00000505441.1:n.*665_*667del
ENST00000680964.1:c.798_800del ENSP00000505961.1:p.Asp266_Gly267delinsGl...
ENST00000681037.1:c.*2282_*2284del ENSP00000506025.1:n.*2282_*2284del
ENST00000681063.1:c.600-943_600-941del ENSP00000506616.1:n.600-943_600-941del
ENST00000681209.1:c.*453_*455del ENSP00000505877.1:n.*453_*455del
ENST00000681278.1:n.1155_1157del
ENST00000681289.1:n.4793_4795del
ENST00000681361.1:c.*465_*467del ENSP00000506679.1:n.*465_*467del
ENST00000681430.1:c.798_800del ENSP00000506301.1:p.Asp266_Gly267delinsGl...
ENST00000681446.1:c.*380_*382del ENSP00000506244.1:n.*380_*382del
ENST00000681450.1:c.*469_*471del ENSP00000505660.1:n.*469_*471del
ENST00000681548.1:c.*384_*386del ENSP00000505275.1:n.*384_*386del
ENST00000681616.1:c.*457_*459del ENSP00000505111.1:n.*457_*459del
ENST00000681621.1:c.*382_*384del ENSP00000505770.1:n.*382_*384del
ENST00000681680.1:n.2893_2895del
ENST00000681720.1:c.*253_*255del ENSP00000505438.1:n.*253_*255del
ENST00000681730.1:n.1020_1022del
ENST00000681790.1:c.540_542del ENSP00000505130.1:p.Asp180_Gly181delinsGl...
ENST00000681837.1:n.1414_1416del
ENST00000681913.1:n.2922_2924del
ENST00000681916.1:c.*566_*568del ENSP00000506477.1:n.*566_*568del
ENST00000681930.1:n.2922_2924del
ENST00000370834.9:c.897_899del ENSP00000359871.5:p.Asp299_Gly300delinsGl...
ENST00000370841.8:c.798_800del ENSP00000359878.4:p.Asp266_Gly267delinsGl...
ENST00000420607.6:c.810_812del ENSP00000409612.2:p.Asp270_Gly271delinsGl...
ENST00000525808.5:c.*384_*386del ENSP00000434823.1:n.*384_*386del
ENST00000526129.5:c.*582_*584del ENSP00000434092.1:n.*582_*584del
ENST00000526196.5:c.*566_*568del ENSP00000431953.1:n.*566_*568del
ENST00000526930.1:n.571_573del
ENST00000528016.1:c.12_14del ENSP00000434284.1:p.Asp4_Gly5delinsGlu
ENST00000529059.5:n.707_709del
ENST00000530953.6:c.*295_*297del ENSP00000431372.1:n.*295_*297del
ENST00000532207.5:n.528_530del
ENST00000532509.5:c.*562_*564del ENSP00000432522.1:n.*562_*564del
ENST00000534334.5:c.*382_*384del ENSP00000435584.1:n.*382_*384del
ENST00000541113.5:c.690_692del ENSP00000442324.1:p.Asp230_Gly231delinsGl...
NM_000016.5:c.798_800del NP_000007.1:p.Asp266_Gly267delinsGlu
NM_001127328.2:c.810_812del NP_001120800.1:p.Asp270_Gly271delinsGlu
NM_001286042.1:c.690_692del NP_001272971.1:p.Asp230_Gly231delinsGlu
NM_001286043.1:c.897_899del NP_001272972.1:p.Asp299_Gly300delinsGlu
NM_001286044.1:c.231_233del NP_001272973.1:p.Asp77_Gly78delinsGlu
NM_000016.6:c.798_800del MANE Select NP_000007.1:p.Asp266_Gly267delinsGlu
NM_001127328.3:c.810_812del NP_001120800.1:p.Asp270_Gly271delinsGlu
NM_001286042.2:c.690_692del NP_001272971.1:p.Asp230_Gly231delinsGlu
NM_001286043.2:c.897_899del NP_001272972.1:p.Asp299_Gly300delinsGlu
NM_001286044.2:c.231_233del NP_001272973.1:p.Asp77_Gly78delinsGlu