Canonical Allele Identifier: CA340818195
Gene: ACADM HGNC NCBI

Linked Data

gnomAD v4: 1-75761288-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761288A>G , CM000663.2:g.75761288A>G GRCh38
NC_000001.10:g.76226973A>G , CM000663.1:g.76226973A>G GRCh37
NC_000001.9:g.75999561A>G NCBI36
NG_007045.2:g.41931A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1112A>G MANE Select ENSP00000359878.5:p.Asp371Gly
ENST00000473018.3:n.3236A>G
ENST00000532207.6:n.2123A>G
ENST00000541113.6:c.1016A>G ENSP00000442324.2:p.Asp339Gly
ENST00000679509.1:n.2074A>G
ENST00000679530.1:c.*880A>G ENSP00000506454.1:n.*880A>G
ENST00000679615.1:n.3127A>G
ENST00000679687.1:c.674A>G ENSP00000506598.1:p.Asp225Gly
ENST00000679704.1:c.*878A>G ENSP00000505117.1:n.*878A>G
ENST00000679709.1:c.*1075A>G ENSP00000506623.1:n.*1075A>G
ENST00000679976.1:c.*696A>G ENSP00000505565.1:n.*696A>G
ENST00000680166.1:n.4401A>G
ENST00000680315.1:n.995A>G
ENST00000680517.1:c.*500A>G ENSP00000505803.1:n.*500A>G
ENST00000680582.1:n.2074A>G
ENST00000680613.1:c.*605A>G ENSP00000506114.1:n.*605A>G
ENST00000680662.1:c.*1026A>G ENSP00000505080.1:n.*1026A>G
ENST00000680691.1:c.*775A>G ENSP00000506487.1:n.*775A>G
ENST00000680694.1:c.*700A>G ENSP00000505658.1:n.*700A>G
ENST00000680743.1:c.*901A>G ENSP00000505073.1:n.*901A>G
ENST00000680749.1:c.*397A>G ENSP00000505122.1:n.*397A>G
ENST00000680798.1:c.*587A>G ENSP00000505670.1:n.*587A>G
ENST00000680805.1:c.971A>G ENSP00000505447.1:p.Asp324Gly
ENST00000680844.1:c.*896A>G ENSP00000506541.1:n.*896A>G
ENST00000680948.1:c.*979A>G ENSP00000505441.1:n.*979A>G
ENST00000680964.1:c.*205A>G ENSP00000505961.1:n.*205A>G
ENST00000681037.1:c.*2596A>G ENSP00000506025.1:n.*2596A>G
ENST00000681063.1:c.*381A>G ENSP00000506616.1:n.*381A>G
ENST00000681209.1:c.*767A>G ENSP00000505877.1:n.*767A>G
ENST00000681278.1:n.1814A>G
ENST00000681289.1:n.5107A>G
ENST00000681361.1:c.*779A>G ENSP00000506679.1:n.*779A>G
ENST00000681430.1:c.*205A>G ENSP00000506301.1:n.*205A>G
ENST00000681446.1:c.*816A>G ENSP00000506244.1:n.*816A>G
ENST00000681450.1:c.*783A>G ENSP00000505660.1:n.*783A>G
ENST00000681548.1:c.*698A>G ENSP00000505275.1:n.*698A>G
ENST00000681616.1:c.*771A>G ENSP00000505111.1:n.*771A>G
ENST00000681621.1:c.*696A>G ENSP00000505770.1:n.*696A>G
ENST00000681680.1:n.3207A>G
ENST00000681720.1:c.*567A>G ENSP00000505438.1:n.*567A>G
ENST00000681730.1:n.1334A>G
ENST00000681790.1:c.854A>G ENSP00000505130.1:p.Asp285Gly
ENST00000681837.1:n.1728A>G
ENST00000681913.1:n.3358A>G
ENST00000681916.1:c.*880A>G ENSP00000506477.1:n.*880A>G
ENST00000681930.1:n.3236A>G
ENST00000370834.9:c.1211A>G ENSP00000359871.5:p.Asp404Gly
ENST00000370841.8:c.1112A>G ENSP00000359878.4:p.Asp371Gly
ENST00000420607.6:c.1124A>G ENSP00000409612.2:p.Asp375Gly
ENST00000481374.1:n.385A>G
ENST00000525808.5:c.*698A>G ENSP00000434823.1:n.*698A>G
ENST00000526129.5:c.*896A>G ENSP00000434092.1:n.*896A>G
ENST00000526196.5:c.*880A>G ENSP00000431953.1:n.*880A>G
ENST00000528016.1:c.160-7889A>G ENSP00000434284.1:n.160-7889A>G
ENST00000529059.5:n.1021A>G
ENST00000541113.5:c.1004A>G ENSP00000442324.1:p.Asp335Gly
NM_000016.5:c.1112A>G NP_000007.1:p.Asp371Gly
NM_001127328.2:c.1124A>G NP_001120800.1:p.Asp375Gly
NM_001286042.1:c.1004A>G NP_001272971.1:p.Asp335Gly
NM_001286043.1:c.1211A>G NP_001272972.1:p.Asp404Gly
NM_001286044.1:c.545A>G NP_001272973.1:p.Asp182Gly
NM_000016.6:c.1112A>G MANE Select NP_000007.1:p.Asp371Gly
NM_001127328.3:c.1124A>G NP_001120800.1:p.Asp375Gly
NM_001286042.2:c.1004A>G NP_001272971.1:p.Asp335Gly
NM_001286043.2:c.1211A>G NP_001272972.1:p.Asp404Gly
NM_001286044.2:c.545A>G NP_001272973.1:p.Asp182Gly