Canonical Allele Identifier: CA1176715857
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740106A= , CM000663.2:g.75740106A= GRCh38
NC_000001.10:g.76205791A= , CM000663.1:g.76205791A= GRCh37
NC_000001.9:g.75978379A= NCBI36
NG_007045.2:g.20749A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.595A= MANE Select ENSP00000359878.5:p.Asn199=
ENST00000473018.3:n.2719A=
ENST00000541113.6:c.595A= ENSP00000442324.2:p.Asn199=
ENST00000679509.1:n.1557A=
ENST00000679530.1:c.*363A= ENSP00000506454.1:n.*363A=
ENST00000679615.1:n.2719A=
ENST00000679687.1:c.157A= ENSP00000506598.1:p.Asn53=
ENST00000679704.1:c.*361A= ENSP00000505117.1:n.*361A=
ENST00000679709.1:c.*558A= ENSP00000506623.1:n.*558A=
ENST00000679804.1:n.334A=
ENST00000679976.1:c.*179A= ENSP00000505565.1:n.*179A=
ENST00000680166.1:n.3884A=
ENST00000680517.1:c.*92A= ENSP00000505803.1:n.*92A=
ENST00000680582.1:n.1557A=
ENST00000680613.1:c.595A= ENSP00000506114.1:p.Asn199=
ENST00000680662.1:c.*509A= ENSP00000505080.1:n.*509A=
ENST00000680691.1:c.*258A= ENSP00000506487.1:n.*258A=
ENST00000680694.1:c.*183A= ENSP00000505658.1:n.*183A=
ENST00000680743.1:c.*262A= ENSP00000505073.1:n.*262A=
ENST00000680749.1:c.595A= ENSP00000505122.1:p.Asn199=
ENST00000680798.1:c.*179A= ENSP00000505670.1:n.*179A=
ENST00000680805.1:c.595A= ENSP00000505447.1:p.Asn199=
ENST00000680844.1:c.*379A= ENSP00000506541.1:n.*379A=
ENST00000680948.1:c.*462A= ENSP00000505441.1:n.*462A=
ENST00000680964.1:c.595A= ENSP00000505961.1:p.Asn199=
ENST00000681037.1:c.595A= ENSP00000506025.1:p.Asn199=
ENST00000681063.1:c.595A= ENSP00000506616.1:p.Asn199=
ENST00000681209.1:c.*359A= ENSP00000505877.1:n.*359A=
ENST00000681278.1:n.952A=
ENST00000681289.1:n.952A=
ENST00000681361.1:c.*262A= ENSP00000506679.1:n.*262A=
ENST00000681430.1:c.595A= ENSP00000506301.1:p.Asn199=
ENST00000681446.1:c.*177A= ENSP00000506244.1:n.*177A=
ENST00000681450.1:c.*266A= ENSP00000505660.1:n.*266A=
ENST00000681548.1:c.*181A= ENSP00000505275.1:n.*181A=
ENST00000681616.1:c.*363A= ENSP00000505111.1:n.*363A=
ENST00000681621.1:c.*179A= ENSP00000505770.1:n.*179A=
ENST00000681680.1:n.2719A=
ENST00000681720.1:c.*55-5700A= ENSP00000505438.1:n.*55-5700A=
ENST00000681730.1:n.817A=
ENST00000681790.1:c.337A= ENSP00000505130.1:p.Asn113=
ENST00000681837.1:n.1211A=
ENST00000681913.1:n.2719A=
ENST00000681916.1:c.*363A= ENSP00000506477.1:n.*363A=
ENST00000681930.1:n.2719A=
ENST00000370834.9:c.694A= ENSP00000359871.5:p.Asn232=
ENST00000370841.8:c.595A= ENSP00000359878.4:p.Asn199=
ENST00000420607.6:c.607A= ENSP00000409612.2:p.Asn203=
ENST00000525808.5:c.*181A= ENSP00000434823.1:n.*181A=
ENST00000526129.5:c.*379A= ENSP00000434092.1:n.*379A=
ENST00000526196.5:c.*363A= ENSP00000431953.1:n.*363A=
ENST00000526930.1:n.368A=
ENST00000529059.5:n.504A=
ENST00000530953.6:c.*92A= ENSP00000431372.1:n.*92A=
ENST00000532509.5:c.*359A= ENSP00000432522.1:n.*359A=
ENST00000534334.5:c.*179A= ENSP00000435584.1:n.*179A=
ENST00000541113.5:c.487A= ENSP00000442324.1:p.Asn163=
NM_000016.5:c.595A= NP_000007.1:p.Asn199=
NM_001127328.2:c.607A= NP_001120800.1:p.Asn203=
NM_001286042.1:c.487A= NP_001272971.1:p.Asn163=
NM_001286043.1:c.694A= NP_001272972.1:p.Asn232=
NM_001286044.1:c.28A= NP_001272973.1:p.Asn10=
NM_000016.6:c.595A= MANE Select NP_000007.1:p.Asn199=
NM_001127328.3:c.607A= NP_001120800.1:p.Asn203=
NM_001286042.2:c.487A= NP_001272971.1:p.Asn163=
NM_001286043.2:c.694A= NP_001272972.1:p.Asn232=
NM_001286044.2:c.28A= NP_001272973.1:p.Asn10=