Canonical Allele Identifier: CA1176721474
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749545A= , CM000663.2:g.75749545A= GRCh38
NC_000001.10:g.76215230A= , CM000663.1:g.76215230A= GRCh37
NC_000001.9:g.75987818A= NCBI36
NG_007045.2:g.30188A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.835A= MANE Select ENSP00000359878.5:p.Lys279=
ENST00000473018.3:n.2959A=
ENST00000532207.6:n.1724A=
ENST00000541113.6:c.835A= ENSP00000442324.2:p.Lys279=
ENST00000679509.1:n.1797A=
ENST00000679530.1:c.*603A= ENSP00000506454.1:n.*603A=
ENST00000679615.1:n.2850A=
ENST00000679687.1:c.397A= ENSP00000506598.1:p.Lys133=
ENST00000679704.1:c.*601A= ENSP00000505117.1:n.*601A=
ENST00000679709.1:c.*798A= ENSP00000506623.1:n.*798A=
ENST00000679976.1:c.*419A= ENSP00000505565.1:n.*419A=
ENST00000680166.1:n.4124A=
ENST00000680517.1:c.*223A= ENSP00000505803.1:n.*223A=
ENST00000680582.1:n.1797A=
ENST00000680613.1:c.*206A= ENSP00000506114.1:n.*206A=
ENST00000680662.1:c.*749A= ENSP00000505080.1:n.*749A=
ENST00000680691.1:c.*498A= ENSP00000506487.1:n.*498A=
ENST00000680694.1:c.*423A= ENSP00000505658.1:n.*423A=
ENST00000680743.1:c.*502A= ENSP00000505073.1:n.*502A=
ENST00000680749.1:c.*120A= ENSP00000505122.1:n.*120A=
ENST00000680798.1:c.*310A= ENSP00000505670.1:n.*310A=
ENST00000680805.1:c.709-906A= ENSP00000505447.1:n.709-906A=
ENST00000680844.1:c.*619A= ENSP00000506541.1:n.*619A=
ENST00000680948.1:c.*702A= ENSP00000505441.1:n.*702A=
ENST00000680964.1:c.835A= ENSP00000505961.1:p.Lys279=
ENST00000681037.1:c.*2319A= ENSP00000506025.1:n.*2319A=
ENST00000681063.1:c.600-906A= ENSP00000506616.1:n.600-906A=
ENST00000681209.1:c.*490A= ENSP00000505877.1:n.*490A=
ENST00000681278.1:n.1192A=
ENST00000681289.1:n.4830A=
ENST00000681361.1:c.*502A= ENSP00000506679.1:n.*502A=
ENST00000681430.1:c.835A= ENSP00000506301.1:p.Lys279=
ENST00000681446.1:c.*417A= ENSP00000506244.1:n.*417A=
ENST00000681450.1:c.*506A= ENSP00000505660.1:n.*506A=
ENST00000681548.1:c.*421A= ENSP00000505275.1:n.*421A=
ENST00000681616.1:c.*494A= ENSP00000505111.1:n.*494A=
ENST00000681621.1:c.*419A= ENSP00000505770.1:n.*419A=
ENST00000681680.1:n.2930A=
ENST00000681720.1:c.*290A= ENSP00000505438.1:n.*290A=
ENST00000681730.1:n.1057A=
ENST00000681790.1:c.577A= ENSP00000505130.1:p.Lys193=
ENST00000681837.1:n.1451A=
ENST00000681913.1:n.2959A=
ENST00000681916.1:c.*603A= ENSP00000506477.1:n.*603A=
ENST00000681930.1:n.2959A=
ENST00000370834.9:c.934A= ENSP00000359871.5:p.Lys312=
ENST00000370841.8:c.835A= ENSP00000359878.4:p.Lys279=
ENST00000420607.6:c.847A= ENSP00000409612.2:p.Lys283=
ENST00000525808.5:c.*421A= ENSP00000434823.1:n.*421A=
ENST00000526129.5:c.*619A= ENSP00000434092.1:n.*619A=
ENST00000526196.5:c.*603A= ENSP00000431953.1:n.*603A=
ENST00000528016.1:c.49A= ENSP00000434284.1:p.Lys17=
ENST00000529059.5:n.744A=
ENST00000532207.5:n.565A=
ENST00000532509.5:c.*599A= ENSP00000432522.1:n.*599A=
ENST00000534334.5:c.*419A= ENSP00000435584.1:n.*419A=
ENST00000541113.5:c.727A= ENSP00000442324.1:p.Lys243=
NM_000016.5:c.835A= NP_000007.1:p.Lys279=
NM_001127328.2:c.847A= NP_001120800.1:p.Lys283=
NM_001286042.1:c.727A= NP_001272971.1:p.Lys243=
NM_001286043.1:c.934A= NP_001272972.1:p.Lys312=
NM_001286044.1:c.268A= NP_001272973.1:p.Lys90=
NM_000016.6:c.835A= MANE Select NP_000007.1:p.Lys279=
NM_001127328.3:c.847A= NP_001120800.1:p.Lys283=
NM_001286042.2:c.727A= NP_001272971.1:p.Lys243=
NM_001286043.2:c.934A= NP_001272972.1:p.Lys312=
NM_001286044.2:c.268A= NP_001272973.1:p.Lys90=