Canonical Allele Identifier: CA340818229
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761306G>T , CM000663.2:g.75761306G>T GRCh38
NC_000001.10:g.76226991G>T , CM000663.1:g.76226991G>T GRCh37
NC_000001.9:g.75999579G>T NCBI36
NG_007045.2:g.41949G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1130G>T MANE Select ENSP00000359878.5:p.Gly377Val
ENST00000473018.3:n.3254G>T
ENST00000532207.6:n.2141G>T
ENST00000541113.6:c.1034G>T ENSP00000442324.2:p.Gly345Val
ENST00000679509.1:n.2092G>T
ENST00000679530.1:c.*898G>T ENSP00000506454.1:n.*898G>T
ENST00000679615.1:n.3145G>T
ENST00000679687.1:c.692G>T ENSP00000506598.1:p.Gly231Val
ENST00000679704.1:c.*896G>T ENSP00000505117.1:n.*896G>T
ENST00000679709.1:c.*1093G>T ENSP00000506623.1:n.*1093G>T
ENST00000679976.1:c.*714G>T ENSP00000505565.1:n.*714G>T
ENST00000680166.1:n.4419G>T
ENST00000680315.1:n.1013G>T
ENST00000680517.1:c.*518G>T ENSP00000505803.1:n.*518G>T
ENST00000680582.1:n.2092G>T
ENST00000680613.1:c.*623G>T ENSP00000506114.1:n.*623G>T
ENST00000680662.1:c.*1044G>T ENSP00000505080.1:n.*1044G>T
ENST00000680691.1:c.*793G>T ENSP00000506487.1:n.*793G>T
ENST00000680694.1:c.*718G>T ENSP00000505658.1:n.*718G>T
ENST00000680743.1:c.*919G>T ENSP00000505073.1:n.*919G>T
ENST00000680749.1:c.*415G>T ENSP00000505122.1:n.*415G>T
ENST00000680798.1:c.*605G>T ENSP00000505670.1:n.*605G>T
ENST00000680805.1:c.989G>T ENSP00000505447.1:p.Gly330Val
ENST00000680844.1:c.*914G>T ENSP00000506541.1:n.*914G>T
ENST00000680948.1:c.*997G>T ENSP00000505441.1:n.*997G>T
ENST00000680964.1:c.*223G>T ENSP00000505961.1:n.*223G>T
ENST00000681037.1:c.*2614G>T ENSP00000506025.1:n.*2614G>T
ENST00000681063.1:c.*399G>T ENSP00000506616.1:n.*399G>T
ENST00000681209.1:c.*785G>T ENSP00000505877.1:n.*785G>T
ENST00000681278.1:n.1832G>T
ENST00000681289.1:n.5125G>T
ENST00000681361.1:c.*797G>T ENSP00000506679.1:n.*797G>T
ENST00000681430.1:c.*223G>T ENSP00000506301.1:n.*223G>T
ENST00000681446.1:c.*834G>T ENSP00000506244.1:n.*834G>T
ENST00000681450.1:c.*801G>T ENSP00000505660.1:n.*801G>T
ENST00000681548.1:c.*716G>T ENSP00000505275.1:n.*716G>T
ENST00000681616.1:c.*789G>T ENSP00000505111.1:n.*789G>T
ENST00000681621.1:c.*714G>T ENSP00000505770.1:n.*714G>T
ENST00000681680.1:n.3225G>T
ENST00000681720.1:c.*585G>T ENSP00000505438.1:n.*585G>T
ENST00000681730.1:n.1352G>T
ENST00000681790.1:c.872G>T ENSP00000505130.1:p.Gly291Val
ENST00000681837.1:n.1746G>T
ENST00000681913.1:n.3376G>T
ENST00000681916.1:c.*898G>T ENSP00000506477.1:n.*898G>T
ENST00000681930.1:n.3254G>T
ENST00000370834.9:c.1229G>T ENSP00000359871.5:p.Gly410Val
ENST00000370841.8:c.1130G>T ENSP00000359878.4:p.Gly377Val
ENST00000420607.6:c.1142G>T ENSP00000409612.2:p.Gly381Val
ENST00000481374.1:n.403G>T
ENST00000525808.5:c.*716G>T ENSP00000434823.1:n.*716G>T
ENST00000526129.5:c.*914G>T ENSP00000434092.1:n.*914G>T
ENST00000526196.5:c.*898G>T ENSP00000431953.1:n.*898G>T
ENST00000528016.1:c.160-7871G>T ENSP00000434284.1:n.160-7871G>T
ENST00000529059.5:n.1039G>T
ENST00000541113.5:c.1022G>T ENSP00000442324.1:p.Gly341Val
NM_000016.5:c.1130G>T NP_000007.1:p.Gly377Val
NM_001127328.2:c.1142G>T NP_001120800.1:p.Gly381Val
NM_001286042.1:c.1022G>T NP_001272971.1:p.Gly341Val
NM_001286043.1:c.1229G>T NP_001272972.1:p.Gly410Val
NM_001286044.1:c.563G>T NP_001272973.1:p.Gly188Val
NM_000016.6:c.1130G>T MANE Select NP_000007.1:p.Gly377Val
NM_001127328.3:c.1142G>T NP_001120800.1:p.Gly381Val
NM_001286042.2:c.1022G>T NP_001272971.1:p.Gly341Val
NM_001286043.2:c.1229G>T NP_001272972.1:p.Gly410Val
NM_001286044.2:c.563G>T NP_001272973.1:p.Gly188Val