Canonical Allele Identifier: CA1176726859
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761265T= , CM000663.2:g.75761265T= GRCh38
NC_000001.10:g.76226950T= , CM000663.1:g.76226950T= GRCh37
NC_000001.9:g.75999538T= NCBI36
NG_007045.2:g.41908T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1089T= MANE Select ENSP00000359878.5:p.Asp363=
ENST00000473018.3:n.3213T=
ENST00000532207.6:n.2100T=
ENST00000541113.6:c.993T= ENSP00000442324.2:p.Asp331=
ENST00000679509.1:n.2051T=
ENST00000679530.1:c.*857T= ENSP00000506454.1:n.*857T=
ENST00000679615.1:n.3104T=
ENST00000679687.1:c.651T= ENSP00000506598.1:p.Asp217=
ENST00000679704.1:c.*855T= ENSP00000505117.1:n.*855T=
ENST00000679709.1:c.*1052T= ENSP00000506623.1:n.*1052T=
ENST00000679976.1:c.*673T= ENSP00000505565.1:n.*673T=
ENST00000680166.1:n.4378T=
ENST00000680315.1:n.972T=
ENST00000680517.1:c.*477T= ENSP00000505803.1:n.*477T=
ENST00000680582.1:n.2051T=
ENST00000680613.1:c.*582T= ENSP00000506114.1:n.*582T=
ENST00000680662.1:c.*1003T= ENSP00000505080.1:n.*1003T=
ENST00000680691.1:c.*752T= ENSP00000506487.1:n.*752T=
ENST00000680694.1:c.*677T= ENSP00000505658.1:n.*677T=
ENST00000680743.1:c.*878T= ENSP00000505073.1:n.*878T=
ENST00000680749.1:c.*374T= ENSP00000505122.1:n.*374T=
ENST00000680798.1:c.*564T= ENSP00000505670.1:n.*564T=
ENST00000680805.1:c.948T= ENSP00000505447.1:p.Asp316=
ENST00000680844.1:c.*873T= ENSP00000506541.1:n.*873T=
ENST00000680948.1:c.*956T= ENSP00000505441.1:n.*956T=
ENST00000680964.1:c.*182T= ENSP00000505961.1:n.*182T=
ENST00000681037.1:c.*2573T= ENSP00000506025.1:n.*2573T=
ENST00000681063.1:c.*358T= ENSP00000506616.1:n.*358T=
ENST00000681209.1:c.*744T= ENSP00000505877.1:n.*744T=
ENST00000681278.1:n.1791T=
ENST00000681289.1:n.5084T=
ENST00000681361.1:c.*756T= ENSP00000506679.1:n.*756T=
ENST00000681430.1:c.*182T= ENSP00000506301.1:n.*182T=
ENST00000681446.1:c.*793T= ENSP00000506244.1:n.*793T=
ENST00000681450.1:c.*760T= ENSP00000505660.1:n.*760T=
ENST00000681548.1:c.*675T= ENSP00000505275.1:n.*675T=
ENST00000681616.1:c.*748T= ENSP00000505111.1:n.*748T=
ENST00000681621.1:c.*673T= ENSP00000505770.1:n.*673T=
ENST00000681680.1:n.3184T=
ENST00000681720.1:c.*544T= ENSP00000505438.1:n.*544T=
ENST00000681730.1:n.1311T=
ENST00000681790.1:c.831T= ENSP00000505130.1:p.Asp277=
ENST00000681837.1:n.1705T=
ENST00000681913.1:n.3335T=
ENST00000681916.1:c.*857T= ENSP00000506477.1:n.*857T=
ENST00000681930.1:n.3213T=
ENST00000370834.9:c.1188T= ENSP00000359871.5:p.Asp396=
ENST00000370841.8:c.1089T= ENSP00000359878.4:p.Asp363=
ENST00000420607.6:c.1101T= ENSP00000409612.2:p.Asp367=
ENST00000481374.1:n.362T=
ENST00000525808.5:c.*675T= ENSP00000434823.1:n.*675T=
ENST00000526129.5:c.*873T= ENSP00000434092.1:n.*873T=
ENST00000526196.5:c.*857T= ENSP00000431953.1:n.*857T=
ENST00000528016.1:c.160-7912T= ENSP00000434284.1:n.160-7912T=
ENST00000529059.5:n.998T=
ENST00000541113.5:c.981T= ENSP00000442324.1:p.Asp327=
NM_000016.5:c.1089T= NP_000007.1:p.Asp363=
NM_001127328.2:c.1101T= NP_001120800.1:p.Asp367=
NM_001286042.1:c.981T= NP_001272971.1:p.Asp327=
NM_001286043.1:c.1188T= NP_001272972.1:p.Asp396=
NM_001286044.1:c.522T= NP_001272973.1:p.Asp174=
NM_000016.6:c.1089T= MANE Select NP_000007.1:p.Asp363=
NM_001127328.3:c.1101T= NP_001120800.1:p.Asp367=
NM_001286042.2:c.981T= NP_001272971.1:p.Asp327=
NM_001286043.2:c.1188T= NP_001272972.1:p.Asp396=
NM_001286044.2:c.522T= NP_001272973.1:p.Asp174=