Canonical Allele Identifier: CA1176726883
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761344C= , CM000663.2:g.75761344C= GRCh38
NC_000001.10:g.76227029C= , CM000663.1:g.76227029C= GRCh37
NC_000001.9:g.75999617C= NCBI36
NG_007045.2:g.41987C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1168C= MANE Select ENSP00000359878.5:p.Leu390=
ENST00000473018.3:n.3292C=
ENST00000532207.6:n.2179C=
ENST00000541113.6:c.1072C= ENSP00000442324.2:p.Leu358=
ENST00000679509.1:n.2130C=
ENST00000679530.1:c.*936C= ENSP00000506454.1:n.*936C=
ENST00000679615.1:n.3183C=
ENST00000679687.1:c.730C= ENSP00000506598.1:p.Leu244=
ENST00000679704.1:c.*934C= ENSP00000505117.1:n.*934C=
ENST00000679709.1:c.*1131C= ENSP00000506623.1:n.*1131C=
ENST00000679976.1:c.*752C= ENSP00000505565.1:n.*752C=
ENST00000680166.1:n.4457C=
ENST00000680315.1:n.1051C=
ENST00000680517.1:c.*556C= ENSP00000505803.1:n.*556C=
ENST00000680582.1:n.2130C=
ENST00000680613.1:c.*661C= ENSP00000506114.1:n.*661C=
ENST00000680662.1:c.*1082C= ENSP00000505080.1:n.*1082C=
ENST00000680691.1:c.*831C= ENSP00000506487.1:n.*831C=
ENST00000680694.1:c.*756C= ENSP00000505658.1:n.*756C=
ENST00000680743.1:c.*957C= ENSP00000505073.1:n.*957C=
ENST00000680749.1:c.*453C= ENSP00000505122.1:n.*453C=
ENST00000680798.1:c.*643C= ENSP00000505670.1:n.*643C=
ENST00000680805.1:c.1027C= ENSP00000505447.1:p.Leu343=
ENST00000680844.1:c.*952C= ENSP00000506541.1:n.*952C=
ENST00000680948.1:c.*1035C= ENSP00000505441.1:n.*1035C=
ENST00000680964.1:c.*261C= ENSP00000505961.1:n.*261C=
ENST00000681037.1:c.*2652C= ENSP00000506025.1:n.*2652C=
ENST00000681063.1:c.*437C= ENSP00000506616.1:n.*437C=
ENST00000681209.1:c.*823C= ENSP00000505877.1:n.*823C=
ENST00000681278.1:n.1870C=
ENST00000681289.1:n.5163C=
ENST00000681361.1:c.*835C= ENSP00000506679.1:n.*835C=
ENST00000681430.1:c.*261C= ENSP00000506301.1:n.*261C=
ENST00000681446.1:c.*872C= ENSP00000506244.1:n.*872C=
ENST00000681450.1:c.*839C= ENSP00000505660.1:n.*839C=
ENST00000681548.1:c.*754C= ENSP00000505275.1:n.*754C=
ENST00000681616.1:c.*827C= ENSP00000505111.1:n.*827C=
ENST00000681621.1:c.*752C= ENSP00000505770.1:n.*752C=
ENST00000681680.1:n.3263C=
ENST00000681720.1:c.*623C= ENSP00000505438.1:n.*623C=
ENST00000681730.1:n.1390C=
ENST00000681790.1:c.910C= ENSP00000505130.1:p.Leu304=
ENST00000681837.1:n.1784C=
ENST00000681913.1:n.3414C=
ENST00000681916.1:c.*936C= ENSP00000506477.1:n.*936C=
ENST00000681930.1:n.3292C=
ENST00000370834.9:c.1267C= ENSP00000359871.5:p.Leu423=
ENST00000370841.8:c.1168C= ENSP00000359878.4:p.Leu390=
ENST00000420607.6:c.1180C= ENSP00000409612.2:p.Leu394=
ENST00000481374.1:n.441C=
ENST00000525808.5:c.*754C= ENSP00000434823.1:n.*754C=
ENST00000526129.5:c.*952C= ENSP00000434092.1:n.*952C=
ENST00000526196.5:c.*936C= ENSP00000431953.1:n.*936C=
ENST00000528016.1:c.160-7833C= ENSP00000434284.1:n.160-7833C=
ENST00000529059.5:n.1077C=
ENST00000541113.5:c.1060C= ENSP00000442324.1:p.Leu354=
NM_000016.5:c.1168C= NP_000007.1:p.Leu390=
NM_001127328.2:c.1180C= NP_001120800.1:p.Leu394=
NM_001286042.1:c.1060C= NP_001272971.1:p.Leu354=
NM_001286043.1:c.1267C= NP_001272972.1:p.Leu423=
NM_001286044.1:c.601C= NP_001272973.1:p.Leu201=
NM_000016.6:c.1168C= MANE Select NP_000007.1:p.Leu390=
NM_001127328.3:c.1180C= NP_001120800.1:p.Leu394=
NM_001286042.2:c.1060C= NP_001272971.1:p.Leu354=
NM_001286043.2:c.1267C= NP_001272972.1:p.Leu423=
NM_001286044.2:c.601C= NP_001272973.1:p.Leu201=