Canonical Allele Identifier: CA913278
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 642376
dbSNP Id: rs201809827
gnomAD v2: 1-76226986-A-G
gnomAD v3: 1-75761301-A-G
gnomAD v4: 1-75761301-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761301A>G , CM000663.2:g.75761301A>G GRCh38
NC_000001.10:g.76226986A>G , CM000663.1:g.76226986A>G GRCh37
NC_000001.9:g.75999574A>G NCBI36
NG_007045.2:g.41944A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1125A>G MANE Select ENSP00000359878.5:p.Ile375Met
ENST00000473018.3:n.3249A>G
ENST00000532207.6:n.2136A>G
ENST00000541113.6:c.1029A>G ENSP00000442324.2:p.Ile343Met
ENST00000679509.1:n.2087A>G
ENST00000679530.1:c.*893A>G ENSP00000506454.1:n.*893A>G
ENST00000679615.1:n.3140A>G
ENST00000679687.1:c.687A>G ENSP00000506598.1:p.Ile229Met
ENST00000679704.1:c.*891A>G ENSP00000505117.1:n.*891A>G
ENST00000679709.1:c.*1088A>G ENSP00000506623.1:n.*1088A>G
ENST00000679976.1:c.*709A>G ENSP00000505565.1:n.*709A>G
ENST00000680166.1:n.4414A>G
ENST00000680315.1:n.1008A>G
ENST00000680517.1:c.*513A>G ENSP00000505803.1:n.*513A>G
ENST00000680582.1:n.2087A>G
ENST00000680613.1:c.*618A>G ENSP00000506114.1:n.*618A>G
ENST00000680662.1:c.*1039A>G ENSP00000505080.1:n.*1039A>G
ENST00000680691.1:c.*788A>G ENSP00000506487.1:n.*788A>G
ENST00000680694.1:c.*713A>G ENSP00000505658.1:n.*713A>G
ENST00000680743.1:c.*914A>G ENSP00000505073.1:n.*914A>G
ENST00000680749.1:c.*410A>G ENSP00000505122.1:n.*410A>G
ENST00000680798.1:c.*600A>G ENSP00000505670.1:n.*600A>G
ENST00000680805.1:c.984A>G ENSP00000505447.1:p.Ile328Met
ENST00000680844.1:c.*909A>G ENSP00000506541.1:n.*909A>G
ENST00000680948.1:c.*992A>G ENSP00000505441.1:n.*992A>G
ENST00000680964.1:c.*218A>G ENSP00000505961.1:n.*218A>G
ENST00000681037.1:c.*2609A>G ENSP00000506025.1:n.*2609A>G
ENST00000681063.1:c.*394A>G ENSP00000506616.1:n.*394A>G
ENST00000681209.1:c.*780A>G ENSP00000505877.1:n.*780A>G
ENST00000681278.1:n.1827A>G
ENST00000681289.1:n.5120A>G
ENST00000681361.1:c.*792A>G ENSP00000506679.1:n.*792A>G
ENST00000681430.1:c.*218A>G ENSP00000506301.1:n.*218A>G
ENST00000681446.1:c.*829A>G ENSP00000506244.1:n.*829A>G
ENST00000681450.1:c.*796A>G ENSP00000505660.1:n.*796A>G
ENST00000681548.1:c.*711A>G ENSP00000505275.1:n.*711A>G
ENST00000681616.1:c.*784A>G ENSP00000505111.1:n.*784A>G
ENST00000681621.1:c.*709A>G ENSP00000505770.1:n.*709A>G
ENST00000681680.1:n.3220A>G
ENST00000681720.1:c.*580A>G ENSP00000505438.1:n.*580A>G
ENST00000681730.1:n.1347A>G
ENST00000681790.1:c.867A>G ENSP00000505130.1:p.Ile289Met
ENST00000681837.1:n.1741A>G
ENST00000681913.1:n.3371A>G
ENST00000681916.1:c.*893A>G ENSP00000506477.1:n.*893A>G
ENST00000681930.1:n.3249A>G
ENST00000370834.9:c.1224A>G ENSP00000359871.5:p.Ile408Met
ENST00000370841.8:c.1125A>G ENSP00000359878.4:p.Ile375Met
ENST00000420607.6:c.1137A>G ENSP00000409612.2:p.Ile379Met
ENST00000481374.1:n.398A>G
ENST00000525808.5:c.*711A>G ENSP00000434823.1:n.*711A>G
ENST00000526129.5:c.*909A>G ENSP00000434092.1:n.*909A>G
ENST00000526196.5:c.*893A>G ENSP00000431953.1:n.*893A>G
ENST00000528016.1:c.160-7876A>G ENSP00000434284.1:n.160-7876A>G
ENST00000529059.5:n.1034A>G
ENST00000541113.5:c.1017A>G ENSP00000442324.1:p.Ile339Met
NM_000016.5:c.1125A>G NP_000007.1:p.Ile375Met
NM_001127328.2:c.1137A>G NP_001120800.1:p.Ile379Met
NM_001286042.1:c.1017A>G NP_001272971.1:p.Ile339Met
NM_001286043.1:c.1224A>G NP_001272972.1:p.Ile408Met
NM_001286044.1:c.558A>G NP_001272973.1:p.Ile186Met
NM_000016.6:c.1125A>G MANE Select NP_000007.1:p.Ile375Met
NM_001127328.3:c.1137A>G NP_001120800.1:p.Ile379Met
NM_001286042.2:c.1017A>G NP_001272971.1:p.Ile339Met
NM_001286043.2:c.1224A>G NP_001272972.1:p.Ile408Met
NM_001286044.2:c.558A>G NP_001272973.1:p.Ile186Met