Canonical Allele Identifier: CA1176726882
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761343A= , CM000663.2:g.75761343A= GRCh38
NC_000001.10:g.76227028A= , CM000663.1:g.76227028A= GRCh37
NC_000001.9:g.75999616A= NCBI36
NG_007045.2:g.41986A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1167A= MANE Select ENSP00000359878.5:p.Lys389=
ENST00000473018.3:n.3291A=
ENST00000532207.6:n.2178A=
ENST00000541113.6:c.1071A= ENSP00000442324.2:p.Lys357=
ENST00000679509.1:n.2129A=
ENST00000679530.1:c.*935A= ENSP00000506454.1:n.*935A=
ENST00000679615.1:n.3182A=
ENST00000679687.1:c.729A= ENSP00000506598.1:p.Lys243=
ENST00000679704.1:c.*933A= ENSP00000505117.1:n.*933A=
ENST00000679709.1:c.*1130A= ENSP00000506623.1:n.*1130A=
ENST00000679976.1:c.*751A= ENSP00000505565.1:n.*751A=
ENST00000680166.1:n.4456A=
ENST00000680315.1:n.1050A=
ENST00000680517.1:c.*555A= ENSP00000505803.1:n.*555A=
ENST00000680582.1:n.2129A=
ENST00000680613.1:c.*660A= ENSP00000506114.1:n.*660A=
ENST00000680662.1:c.*1081A= ENSP00000505080.1:n.*1081A=
ENST00000680691.1:c.*830A= ENSP00000506487.1:n.*830A=
ENST00000680694.1:c.*755A= ENSP00000505658.1:n.*755A=
ENST00000680743.1:c.*956A= ENSP00000505073.1:n.*956A=
ENST00000680749.1:c.*452A= ENSP00000505122.1:n.*452A=
ENST00000680798.1:c.*642A= ENSP00000505670.1:n.*642A=
ENST00000680805.1:c.1026A= ENSP00000505447.1:p.Lys342=
ENST00000680844.1:c.*951A= ENSP00000506541.1:n.*951A=
ENST00000680948.1:c.*1034A= ENSP00000505441.1:n.*1034A=
ENST00000680964.1:c.*260A= ENSP00000505961.1:n.*260A=
ENST00000681037.1:c.*2651A= ENSP00000506025.1:n.*2651A=
ENST00000681063.1:c.*436A= ENSP00000506616.1:n.*436A=
ENST00000681209.1:c.*822A= ENSP00000505877.1:n.*822A=
ENST00000681278.1:n.1869A=
ENST00000681289.1:n.5162A=
ENST00000681361.1:c.*834A= ENSP00000506679.1:n.*834A=
ENST00000681430.1:c.*260A= ENSP00000506301.1:n.*260A=
ENST00000681446.1:c.*871A= ENSP00000506244.1:n.*871A=
ENST00000681450.1:c.*838A= ENSP00000505660.1:n.*838A=
ENST00000681548.1:c.*753A= ENSP00000505275.1:n.*753A=
ENST00000681616.1:c.*826A= ENSP00000505111.1:n.*826A=
ENST00000681621.1:c.*751A= ENSP00000505770.1:n.*751A=
ENST00000681680.1:n.3262A=
ENST00000681720.1:c.*622A= ENSP00000505438.1:n.*622A=
ENST00000681730.1:n.1389A=
ENST00000681790.1:c.909A= ENSP00000505130.1:p.Lys303=
ENST00000681837.1:n.1783A=
ENST00000681913.1:n.3413A=
ENST00000681916.1:c.*935A= ENSP00000506477.1:n.*935A=
ENST00000681930.1:n.3291A=
ENST00000370834.9:c.1266A= ENSP00000359871.5:p.Lys422=
ENST00000370841.8:c.1167A= ENSP00000359878.4:p.Lys389=
ENST00000420607.6:c.1179A= ENSP00000409612.2:p.Lys393=
ENST00000481374.1:n.440A=
ENST00000525808.5:c.*753A= ENSP00000434823.1:n.*753A=
ENST00000526129.5:c.*951A= ENSP00000434092.1:n.*951A=
ENST00000526196.5:c.*935A= ENSP00000431953.1:n.*935A=
ENST00000528016.1:c.160-7834A= ENSP00000434284.1:n.160-7834A=
ENST00000529059.5:n.1076A=
ENST00000541113.5:c.1059A= ENSP00000442324.1:p.Lys353=
NM_000016.5:c.1167A= NP_000007.1:p.Lys389=
NM_001127328.2:c.1179A= NP_001120800.1:p.Lys393=
NM_001286042.1:c.1059A= NP_001272971.1:p.Lys353=
NM_001286043.1:c.1266A= NP_001272972.1:p.Lys422=
NM_001286044.1:c.600A= NP_001272973.1:p.Lys200=
NM_000016.6:c.1167A= MANE Select NP_000007.1:p.Lys389=
NM_001127328.3:c.1179A= NP_001120800.1:p.Lys393=
NM_001286042.2:c.1059A= NP_001272971.1:p.Lys353=
NM_001286043.2:c.1266A= NP_001272972.1:p.Lys422=
NM_001286044.2:c.600A= NP_001272973.1:p.Lys200=