Canonical Allele Identifier: CA340818313
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761345T>G , CM000663.2:g.75761345T>G GRCh38
NC_000001.10:g.76227030T>G , CM000663.1:g.76227030T>G GRCh37
NC_000001.9:g.75999618T>G NCBI36
NG_007045.2:g.41988T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1169T>G MANE Select ENSP00000359878.5:p.Leu390Arg
ENST00000473018.3:n.3293T>G
ENST00000532207.6:n.2180T>G
ENST00000541113.6:c.1073T>G ENSP00000442324.2:p.Leu358Arg
ENST00000679509.1:n.2131T>G
ENST00000679530.1:c.*937T>G ENSP00000506454.1:n.*937T>G
ENST00000679615.1:n.3184T>G
ENST00000679687.1:c.731T>G ENSP00000506598.1:p.Leu244Arg
ENST00000679704.1:c.*935T>G ENSP00000505117.1:n.*935T>G
ENST00000679709.1:c.*1132T>G ENSP00000506623.1:n.*1132T>G
ENST00000679976.1:c.*753T>G ENSP00000505565.1:n.*753T>G
ENST00000680166.1:n.4458T>G
ENST00000680315.1:n.1052T>G
ENST00000680517.1:c.*557T>G ENSP00000505803.1:n.*557T>G
ENST00000680582.1:n.2131T>G
ENST00000680613.1:c.*662T>G ENSP00000506114.1:n.*662T>G
ENST00000680662.1:c.*1083T>G ENSP00000505080.1:n.*1083T>G
ENST00000680691.1:c.*832T>G ENSP00000506487.1:n.*832T>G
ENST00000680694.1:c.*757T>G ENSP00000505658.1:n.*757T>G
ENST00000680743.1:c.*958T>G ENSP00000505073.1:n.*958T>G
ENST00000680749.1:c.*454T>G ENSP00000505122.1:n.*454T>G
ENST00000680798.1:c.*644T>G ENSP00000505670.1:n.*644T>G
ENST00000680805.1:c.1028T>G ENSP00000505447.1:p.Leu343Arg
ENST00000680844.1:c.*953T>G ENSP00000506541.1:n.*953T>G
ENST00000680948.1:c.*1036T>G ENSP00000505441.1:n.*1036T>G
ENST00000680964.1:c.*262T>G ENSP00000505961.1:n.*262T>G
ENST00000681037.1:c.*2653T>G ENSP00000506025.1:n.*2653T>G
ENST00000681063.1:c.*438T>G ENSP00000506616.1:n.*438T>G
ENST00000681209.1:c.*824T>G ENSP00000505877.1:n.*824T>G
ENST00000681278.1:n.1871T>G
ENST00000681289.1:n.5164T>G
ENST00000681361.1:c.*836T>G ENSP00000506679.1:n.*836T>G
ENST00000681430.1:c.*262T>G ENSP00000506301.1:n.*262T>G
ENST00000681446.1:c.*873T>G ENSP00000506244.1:n.*873T>G
ENST00000681450.1:c.*840T>G ENSP00000505660.1:n.*840T>G
ENST00000681548.1:c.*755T>G ENSP00000505275.1:n.*755T>G
ENST00000681616.1:c.*828T>G ENSP00000505111.1:n.*828T>G
ENST00000681621.1:c.*753T>G ENSP00000505770.1:n.*753T>G
ENST00000681680.1:n.3264T>G
ENST00000681720.1:c.*624T>G ENSP00000505438.1:n.*624T>G
ENST00000681730.1:n.1391T>G
ENST00000681790.1:c.911T>G ENSP00000505130.1:p.Leu304Arg
ENST00000681837.1:n.1785T>G
ENST00000681913.1:n.3415T>G
ENST00000681916.1:c.*937T>G ENSP00000506477.1:n.*937T>G
ENST00000681930.1:n.3293T>G
ENST00000370834.9:c.1268T>G ENSP00000359871.5:p.Leu423Arg
ENST00000370841.8:c.1169T>G ENSP00000359878.4:p.Leu390Arg
ENST00000420607.6:c.1181T>G ENSP00000409612.2:p.Leu394Arg
ENST00000481374.1:n.442T>G
ENST00000525808.5:c.*755T>G ENSP00000434823.1:n.*755T>G
ENST00000526129.5:c.*953T>G ENSP00000434092.1:n.*953T>G
ENST00000526196.5:c.*937T>G ENSP00000431953.1:n.*937T>G
ENST00000528016.1:c.160-7832T>G ENSP00000434284.1:n.160-7832T>G
ENST00000529059.5:n.1078T>G
ENST00000541113.5:c.1061T>G ENSP00000442324.1:p.Leu354Arg
NM_000016.5:c.1169T>G NP_000007.1:p.Leu390Arg
NM_001127328.2:c.1181T>G NP_001120800.1:p.Leu394Arg
NM_001286042.1:c.1061T>G NP_001272971.1:p.Leu354Arg
NM_001286043.1:c.1268T>G NP_001272972.1:p.Leu423Arg
NM_001286044.1:c.602T>G NP_001272973.1:p.Leu201Arg
NM_000016.6:c.1169T>G MANE Select NP_000007.1:p.Leu390Arg
NM_001127328.3:c.1181T>G NP_001120800.1:p.Leu394Arg
NM_001286042.2:c.1061T>G NP_001272971.1:p.Leu354Arg
NM_001286043.2:c.1268T>G NP_001272972.1:p.Leu423Arg
NM_001286044.2:c.602T>G NP_001272973.1:p.Leu201Arg