Canonical Allele Identifier: CA340817978
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761185T>G , CM000663.2:g.75761185T>G GRCh38
NC_000001.10:g.76226870T>G , CM000663.1:g.76226870T>G GRCh37
NC_000001.9:g.75999458T>G NCBI36
NG_007045.2:g.41828T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1009T>G MANE Select ENSP00000359878.5:p.Tyr337Asp
ENST00000473018.3:n.3133T>G
ENST00000532207.6:n.2020T>G
ENST00000541113.6:c.913T>G ENSP00000442324.2:p.Tyr305Asp
ENST00000679509.1:n.1971T>G
ENST00000679530.1:c.*777T>G ENSP00000506454.1:n.*777T>G
ENST00000679615.1:n.3024T>G
ENST00000679687.1:c.571T>G ENSP00000506598.1:p.Tyr191Asp
ENST00000679704.1:c.*775T>G ENSP00000505117.1:n.*775T>G
ENST00000679709.1:c.*972T>G ENSP00000506623.1:n.*972T>G
ENST00000679976.1:c.*593T>G ENSP00000505565.1:n.*593T>G
ENST00000680166.1:n.4298T>G
ENST00000680315.1:n.892T>G
ENST00000680517.1:c.*397T>G ENSP00000505803.1:n.*397T>G
ENST00000680582.1:n.1971T>G
ENST00000680613.1:c.*502T>G ENSP00000506114.1:n.*502T>G
ENST00000680662.1:c.*923T>G ENSP00000505080.1:n.*923T>G
ENST00000680691.1:c.*672T>G ENSP00000506487.1:n.*672T>G
ENST00000680694.1:c.*597T>G ENSP00000505658.1:n.*597T>G
ENST00000680743.1:c.*798T>G ENSP00000505073.1:n.*798T>G
ENST00000680749.1:c.*294T>G ENSP00000505122.1:n.*294T>G
ENST00000680798.1:c.*484T>G ENSP00000505670.1:n.*484T>G
ENST00000680805.1:c.868T>G ENSP00000505447.1:p.Tyr290Asp
ENST00000680844.1:c.*793T>G ENSP00000506541.1:n.*793T>G
ENST00000680948.1:c.*876T>G ENSP00000505441.1:n.*876T>G
ENST00000680964.1:c.*102T>G ENSP00000505961.1:n.*102T>G
ENST00000681037.1:c.*2493T>G ENSP00000506025.1:n.*2493T>G
ENST00000681063.1:c.*278T>G ENSP00000506616.1:n.*278T>G
ENST00000681209.1:c.*664T>G ENSP00000505877.1:n.*664T>G
ENST00000681278.1:n.1711T>G
ENST00000681289.1:n.5004T>G
ENST00000681361.1:c.*676T>G ENSP00000506679.1:n.*676T>G
ENST00000681430.1:c.*102T>G ENSP00000506301.1:n.*102T>G
ENST00000681446.1:c.*713T>G ENSP00000506244.1:n.*713T>G
ENST00000681450.1:c.*680T>G ENSP00000505660.1:n.*680T>G
ENST00000681548.1:c.*595T>G ENSP00000505275.1:n.*595T>G
ENST00000681616.1:c.*668T>G ENSP00000505111.1:n.*668T>G
ENST00000681621.1:c.*593T>G ENSP00000505770.1:n.*593T>G
ENST00000681680.1:n.3104T>G
ENST00000681720.1:c.*464T>G ENSP00000505438.1:n.*464T>G
ENST00000681730.1:n.1231T>G
ENST00000681790.1:c.751T>G ENSP00000505130.1:p.Tyr251Asp
ENST00000681837.1:n.1625T>G
ENST00000681913.1:n.3255T>G
ENST00000681916.1:c.*777T>G ENSP00000506477.1:n.*777T>G
ENST00000681930.1:n.3133T>G
ENST00000370834.9:c.1108T>G ENSP00000359871.5:p.Tyr370Asp
ENST00000370841.8:c.1009T>G ENSP00000359878.4:p.Tyr337Asp
ENST00000420607.6:c.1021T>G ENSP00000409612.2:p.Tyr341Asp
ENST00000481374.1:n.282T>G
ENST00000525808.5:c.*595T>G ENSP00000434823.1:n.*595T>G
ENST00000526129.5:c.*793T>G ENSP00000434092.1:n.*793T>G
ENST00000526196.5:c.*777T>G ENSP00000431953.1:n.*777T>G
ENST00000528016.1:c.160-7992T>G ENSP00000434284.1:n.160-7992T>G
ENST00000529059.5:n.918T>G
ENST00000532207.5:n.739T>G
ENST00000534334.5:c.*750T>G ENSP00000435584.1:n.*750T>G
ENST00000541113.5:c.901T>G ENSP00000442324.1:p.Tyr301Asp
NM_000016.5:c.1009T>G NP_000007.1:p.Tyr337Asp
NM_001127328.2:c.1021T>G NP_001120800.1:p.Tyr341Asp
NM_001286042.1:c.901T>G NP_001272971.1:p.Tyr301Asp
NM_001286043.1:c.1108T>G NP_001272972.1:p.Tyr370Asp
NM_001286044.1:c.442T>G NP_001272973.1:p.Tyr148Asp
NM_000016.6:c.1009T>G MANE Select NP_000007.1:p.Tyr337Asp
NM_001127328.3:c.1021T>G NP_001120800.1:p.Tyr341Asp
NM_001286042.2:c.901T>G NP_001272971.1:p.Tyr301Asp
NM_001286043.2:c.1108T>G NP_001272972.1:p.Tyr370Asp
NM_001286044.2:c.442T>G NP_001272973.1:p.Tyr148Asp