Canonical Allele Identifier: CA340818316
Gene: ACADM HGNC NCBI

Linked Data

dbSNP Id: rs1428129658
gnomAD v2: 1-76227032-A-G
gnomAD v3: 1-75761347-A-G
gnomAD v4: 1-75761347-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761347A>G , CM000663.2:g.75761347A>G GRCh38
NC_000001.10:g.76227032A>G , CM000663.1:g.76227032A>G GRCh37
NC_000001.9:g.75999620A>G NCBI36
NG_007045.2:g.41990A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1171A>G MANE Select ENSP00000359878.5:p.Met391Val
ENST00000473018.3:n.3295A>G
ENST00000532207.6:n.2182A>G
ENST00000541113.6:c.1075A>G ENSP00000442324.2:p.Met359Val
ENST00000679509.1:n.2133A>G
ENST00000679530.1:c.*939A>G ENSP00000506454.1:n.*939A>G
ENST00000679615.1:n.3186A>G
ENST00000679687.1:c.733A>G ENSP00000506598.1:p.Met245Val
ENST00000679704.1:c.*937A>G ENSP00000505117.1:n.*937A>G
ENST00000679709.1:c.*1134A>G ENSP00000506623.1:n.*1134A>G
ENST00000679976.1:c.*755A>G ENSP00000505565.1:n.*755A>G
ENST00000680166.1:n.4460A>G
ENST00000680315.1:n.1054A>G
ENST00000680517.1:c.*559A>G ENSP00000505803.1:n.*559A>G
ENST00000680582.1:n.2133A>G
ENST00000680613.1:c.*664A>G ENSP00000506114.1:n.*664A>G
ENST00000680662.1:c.*1085A>G ENSP00000505080.1:n.*1085A>G
ENST00000680691.1:c.*834A>G ENSP00000506487.1:n.*834A>G
ENST00000680694.1:c.*759A>G ENSP00000505658.1:n.*759A>G
ENST00000680743.1:c.*960A>G ENSP00000505073.1:n.*960A>G
ENST00000680749.1:c.*456A>G ENSP00000505122.1:n.*456A>G
ENST00000680798.1:c.*646A>G ENSP00000505670.1:n.*646A>G
ENST00000680805.1:c.1030A>G ENSP00000505447.1:p.Met344Val
ENST00000680844.1:c.*955A>G ENSP00000506541.1:n.*955A>G
ENST00000680948.1:c.*1038A>G ENSP00000505441.1:n.*1038A>G
ENST00000680964.1:c.*264A>G ENSP00000505961.1:n.*264A>G
ENST00000681037.1:c.*2655A>G ENSP00000506025.1:n.*2655A>G
ENST00000681063.1:c.*440A>G ENSP00000506616.1:n.*440A>G
ENST00000681209.1:c.*826A>G ENSP00000505877.1:n.*826A>G
ENST00000681278.1:n.1873A>G
ENST00000681289.1:n.5166A>G
ENST00000681361.1:c.*838A>G ENSP00000506679.1:n.*838A>G
ENST00000681430.1:c.*264A>G ENSP00000506301.1:n.*264A>G
ENST00000681446.1:c.*875A>G ENSP00000506244.1:n.*875A>G
ENST00000681450.1:c.*842A>G ENSP00000505660.1:n.*842A>G
ENST00000681548.1:c.*757A>G ENSP00000505275.1:n.*757A>G
ENST00000681616.1:c.*830A>G ENSP00000505111.1:n.*830A>G
ENST00000681621.1:c.*755A>G ENSP00000505770.1:n.*755A>G
ENST00000681680.1:n.3266A>G
ENST00000681720.1:c.*626A>G ENSP00000505438.1:n.*626A>G
ENST00000681730.1:n.1393A>G
ENST00000681790.1:c.913A>G ENSP00000505130.1:p.Met305Val
ENST00000681837.1:n.1787A>G
ENST00000681913.1:n.3417A>G
ENST00000681916.1:c.*939A>G ENSP00000506477.1:n.*939A>G
ENST00000681930.1:n.3295A>G
ENST00000370834.9:c.1270A>G ENSP00000359871.5:p.Met424Val
ENST00000370841.8:c.1171A>G ENSP00000359878.4:p.Met391Val
ENST00000420607.6:c.1183A>G ENSP00000409612.2:p.Met395Val
ENST00000481374.1:n.444A>G
ENST00000525808.5:c.*757A>G ENSP00000434823.1:n.*757A>G
ENST00000526129.5:c.*955A>G ENSP00000434092.1:n.*955A>G
ENST00000526196.5:c.*939A>G ENSP00000431953.1:n.*939A>G
ENST00000528016.1:c.160-7830A>G ENSP00000434284.1:n.160-7830A>G
ENST00000529059.5:n.1080A>G
ENST00000541113.5:c.1063A>G ENSP00000442324.1:p.Met355Val
NM_000016.5:c.1171A>G NP_000007.1:p.Met391Val
NM_001127328.2:c.1183A>G NP_001120800.1:p.Met395Val
NM_001286042.1:c.1063A>G NP_001272971.1:p.Met355Val
NM_001286043.1:c.1270A>G NP_001272972.1:p.Met424Val
NM_001286044.1:c.604A>G NP_001272973.1:p.Met202Val
NM_000016.6:c.1171A>G MANE Select NP_000007.1:p.Met391Val
NM_001127328.3:c.1183A>G NP_001120800.1:p.Met395Val
NM_001286042.2:c.1063A>G NP_001272971.1:p.Met355Val
NM_001286043.2:c.1270A>G NP_001272972.1:p.Met424Val
NM_001286044.2:c.604A>G NP_001272973.1:p.Met202Val