Canonical Allele Identifier: CA418707740
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76226992A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761307A>G , CM000663.2:g.75761307A>G GRCh38
NC_000001.10:g.76226992A>G , CM000663.1:g.76226992A>G GRCh37
NC_000001.9:g.75999580A>G NCBI36
NG_007045.2:g.41950A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1131A>G MANE Select ENSP00000359878.5:p.Gly377=
ENST00000473018.3:n.3255A>G
ENST00000532207.6:n.2142A>G
ENST00000541113.6:c.1035A>G ENSP00000442324.2:p.Gly345=
ENST00000679509.1:n.2093A>G
ENST00000679530.1:c.*899A>G ENSP00000506454.1:n.*899A>G
ENST00000679615.1:n.3146A>G
ENST00000679687.1:c.693A>G ENSP00000506598.1:p.Gly231=
ENST00000679704.1:c.*897A>G ENSP00000505117.1:n.*897A>G
ENST00000679709.1:c.*1094A>G ENSP00000506623.1:n.*1094A>G
ENST00000679976.1:c.*715A>G ENSP00000505565.1:n.*715A>G
ENST00000680166.1:n.4420A>G
ENST00000680315.1:n.1014A>G
ENST00000680517.1:c.*519A>G ENSP00000505803.1:n.*519A>G
ENST00000680582.1:n.2093A>G
ENST00000680613.1:c.*624A>G ENSP00000506114.1:n.*624A>G
ENST00000680662.1:c.*1045A>G ENSP00000505080.1:n.*1045A>G
ENST00000680691.1:c.*794A>G ENSP00000506487.1:n.*794A>G
ENST00000680694.1:c.*719A>G ENSP00000505658.1:n.*719A>G
ENST00000680743.1:c.*920A>G ENSP00000505073.1:n.*920A>G
ENST00000680749.1:c.*416A>G ENSP00000505122.1:n.*416A>G
ENST00000680798.1:c.*606A>G ENSP00000505670.1:n.*606A>G
ENST00000680805.1:c.990A>G ENSP00000505447.1:p.Gly330=
ENST00000680844.1:c.*915A>G ENSP00000506541.1:n.*915A>G
ENST00000680948.1:c.*998A>G ENSP00000505441.1:n.*998A>G
ENST00000680964.1:c.*224A>G ENSP00000505961.1:n.*224A>G
ENST00000681037.1:c.*2615A>G ENSP00000506025.1:n.*2615A>G
ENST00000681063.1:c.*400A>G ENSP00000506616.1:n.*400A>G
ENST00000681209.1:c.*786A>G ENSP00000505877.1:n.*786A>G
ENST00000681278.1:n.1833A>G
ENST00000681289.1:n.5126A>G
ENST00000681361.1:c.*798A>G ENSP00000506679.1:n.*798A>G
ENST00000681430.1:c.*224A>G ENSP00000506301.1:n.*224A>G
ENST00000681446.1:c.*835A>G ENSP00000506244.1:n.*835A>G
ENST00000681450.1:c.*802A>G ENSP00000505660.1:n.*802A>G
ENST00000681548.1:c.*717A>G ENSP00000505275.1:n.*717A>G
ENST00000681616.1:c.*790A>G ENSP00000505111.1:n.*790A>G
ENST00000681621.1:c.*715A>G ENSP00000505770.1:n.*715A>G
ENST00000681680.1:n.3226A>G
ENST00000681720.1:c.*586A>G ENSP00000505438.1:n.*586A>G
ENST00000681730.1:n.1353A>G
ENST00000681790.1:c.873A>G ENSP00000505130.1:p.Gly291=
ENST00000681837.1:n.1747A>G
ENST00000681913.1:n.3377A>G
ENST00000681916.1:c.*899A>G ENSP00000506477.1:n.*899A>G
ENST00000681930.1:n.3255A>G
ENST00000370834.9:c.1230A>G ENSP00000359871.5:p.Gly410=
ENST00000370841.8:c.1131A>G ENSP00000359878.4:p.Gly377=
ENST00000420607.6:c.1143A>G ENSP00000409612.2:p.Gly381=
ENST00000481374.1:n.404A>G
ENST00000525808.5:c.*717A>G ENSP00000434823.1:n.*717A>G
ENST00000526129.5:c.*915A>G ENSP00000434092.1:n.*915A>G
ENST00000526196.5:c.*899A>G ENSP00000431953.1:n.*899A>G
ENST00000528016.1:c.160-7870A>G ENSP00000434284.1:n.160-7870A>G
ENST00000529059.5:n.1040A>G
ENST00000541113.5:c.1023A>G ENSP00000442324.1:p.Gly341=
NM_000016.5:c.1131A>G NP_000007.1:p.Gly377=
NM_001127328.2:c.1143A>G NP_001120800.1:p.Gly381=
NM_001286042.1:c.1023A>G NP_001272971.1:p.Gly341=
NM_001286043.1:c.1230A>G NP_001272972.1:p.Gly410=
NM_001286044.1:c.564A>G NP_001272973.1:p.Gly188=
NM_000016.6:c.1131A>G MANE Select NP_000007.1:p.Gly377=
NM_001127328.3:c.1143A>G NP_001120800.1:p.Gly381=
NM_001286042.2:c.1023A>G NP_001272971.1:p.Gly341=
NM_001286043.2:c.1230A>G NP_001272972.1:p.Gly410=
NM_001286044.2:c.564A>G NP_001272973.1:p.Gly188=