Canonical Allele Identifier: CA418707793
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76227025A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761340A>G , CM000663.2:g.75761340A>G GRCh38
NC_000001.10:g.76227025A>G , CM000663.1:g.76227025A>G GRCh37
NC_000001.9:g.75999613A>G NCBI36
NG_007045.2:g.41983A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1164A>G MANE Select ENSP00000359878.5:p.Glu388=
ENST00000473018.3:n.3288A>G
ENST00000532207.6:n.2175A>G
ENST00000541113.6:c.1068A>G ENSP00000442324.2:p.Glu356=
ENST00000679509.1:n.2126A>G
ENST00000679530.1:c.*932A>G ENSP00000506454.1:n.*932A>G
ENST00000679615.1:n.3179A>G
ENST00000679687.1:c.726A>G ENSP00000506598.1:p.Glu242=
ENST00000679704.1:c.*930A>G ENSP00000505117.1:n.*930A>G
ENST00000679709.1:c.*1127A>G ENSP00000506623.1:n.*1127A>G
ENST00000679976.1:c.*748A>G ENSP00000505565.1:n.*748A>G
ENST00000680166.1:n.4453A>G
ENST00000680315.1:n.1047A>G
ENST00000680517.1:c.*552A>G ENSP00000505803.1:n.*552A>G
ENST00000680582.1:n.2126A>G
ENST00000680613.1:c.*657A>G ENSP00000506114.1:n.*657A>G
ENST00000680662.1:c.*1078A>G ENSP00000505080.1:n.*1078A>G
ENST00000680691.1:c.*827A>G ENSP00000506487.1:n.*827A>G
ENST00000680694.1:c.*752A>G ENSP00000505658.1:n.*752A>G
ENST00000680743.1:c.*953A>G ENSP00000505073.1:n.*953A>G
ENST00000680749.1:c.*449A>G ENSP00000505122.1:n.*449A>G
ENST00000680798.1:c.*639A>G ENSP00000505670.1:n.*639A>G
ENST00000680805.1:c.1023A>G ENSP00000505447.1:p.Glu341=
ENST00000680844.1:c.*948A>G ENSP00000506541.1:n.*948A>G
ENST00000680948.1:c.*1031A>G ENSP00000505441.1:n.*1031A>G
ENST00000680964.1:c.*257A>G ENSP00000505961.1:n.*257A>G
ENST00000681037.1:c.*2648A>G ENSP00000506025.1:n.*2648A>G
ENST00000681063.1:c.*433A>G ENSP00000506616.1:n.*433A>G
ENST00000681209.1:c.*819A>G ENSP00000505877.1:n.*819A>G
ENST00000681278.1:n.1866A>G
ENST00000681289.1:n.5159A>G
ENST00000681361.1:c.*831A>G ENSP00000506679.1:n.*831A>G
ENST00000681430.1:c.*257A>G ENSP00000506301.1:n.*257A>G
ENST00000681446.1:c.*868A>G ENSP00000506244.1:n.*868A>G
ENST00000681450.1:c.*835A>G ENSP00000505660.1:n.*835A>G
ENST00000681548.1:c.*750A>G ENSP00000505275.1:n.*750A>G
ENST00000681616.1:c.*823A>G ENSP00000505111.1:n.*823A>G
ENST00000681621.1:c.*748A>G ENSP00000505770.1:n.*748A>G
ENST00000681680.1:n.3259A>G
ENST00000681720.1:c.*619A>G ENSP00000505438.1:n.*619A>G
ENST00000681730.1:n.1386A>G
ENST00000681790.1:c.906A>G ENSP00000505130.1:p.Glu302=
ENST00000681837.1:n.1780A>G
ENST00000681913.1:n.3410A>G
ENST00000681916.1:c.*932A>G ENSP00000506477.1:n.*932A>G
ENST00000681930.1:n.3288A>G
ENST00000370834.9:c.1263A>G ENSP00000359871.5:p.Glu421=
ENST00000370841.8:c.1164A>G ENSP00000359878.4:p.Glu388=
ENST00000420607.6:c.1176A>G ENSP00000409612.2:p.Glu392=
ENST00000481374.1:n.437A>G
ENST00000525808.5:c.*750A>G ENSP00000434823.1:n.*750A>G
ENST00000526129.5:c.*948A>G ENSP00000434092.1:n.*948A>G
ENST00000526196.5:c.*932A>G ENSP00000431953.1:n.*932A>G
ENST00000528016.1:c.160-7837A>G ENSP00000434284.1:n.160-7837A>G
ENST00000529059.5:n.1073A>G
ENST00000541113.5:c.1056A>G ENSP00000442324.1:p.Glu352=
NM_000016.5:c.1164A>G NP_000007.1:p.Glu388=
NM_001127328.2:c.1176A>G NP_001120800.1:p.Glu392=
NM_001286042.1:c.1056A>G NP_001272971.1:p.Glu352=
NM_001286043.1:c.1263A>G NP_001272972.1:p.Glu421=
NM_001286044.1:c.597A>G NP_001272973.1:p.Glu199=
NM_000016.6:c.1164A>G MANE Select NP_000007.1:p.Glu388=
NM_001127328.3:c.1176A>G NP_001120800.1:p.Glu392=
NM_001286042.2:c.1056A>G NP_001272971.1:p.Glu352=
NM_001286043.2:c.1263A>G NP_001272972.1:p.Glu421=
NM_001286044.2:c.597A>G NP_001272973.1:p.Glu199=