Canonical Allele Identifier: CA1148721691
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761209G= , CM000663.2:g.75761209G= GRCh38
NC_000001.10:g.76226894G= , CM000663.1:g.76226894G= GRCh37
NC_000001.9:g.75999482G= NCBI36
NG_007045.2:g.41852G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1033G= MANE Select ENSP00000359878.5:p.Asp345=
ENST00000473018.3:n.3157G=
ENST00000532207.6:n.2044G=
ENST00000541113.6:c.937G= ENSP00000442324.2:p.Asp313=
ENST00000679509.1:n.1995G=
ENST00000679530.1:c.*801G= ENSP00000506454.1:n.*801G=
ENST00000679615.1:n.3048G=
ENST00000679687.1:c.595G= ENSP00000506598.1:p.Asp199=
ENST00000679704.1:c.*799G= ENSP00000505117.1:n.*799G=
ENST00000679709.1:c.*996G= ENSP00000506623.1:n.*996G=
ENST00000679976.1:c.*617G= ENSP00000505565.1:n.*617G=
ENST00000680166.1:n.4322G=
ENST00000680315.1:n.916G=
ENST00000680517.1:c.*421G= ENSP00000505803.1:n.*421G=
ENST00000680582.1:n.1995G=
ENST00000680613.1:c.*526G= ENSP00000506114.1:n.*526G=
ENST00000680662.1:c.*947G= ENSP00000505080.1:n.*947G=
ENST00000680691.1:c.*696G= ENSP00000506487.1:n.*696G=
ENST00000680694.1:c.*621G= ENSP00000505658.1:n.*621G=
ENST00000680743.1:c.*822G= ENSP00000505073.1:n.*822G=
ENST00000680749.1:c.*318G= ENSP00000505122.1:n.*318G=
ENST00000680798.1:c.*508G= ENSP00000505670.1:n.*508G=
ENST00000680805.1:c.892G= ENSP00000505447.1:p.Asp298=
ENST00000680844.1:c.*817G= ENSP00000506541.1:n.*817G=
ENST00000680948.1:c.*900G= ENSP00000505441.1:n.*900G=
ENST00000680964.1:c.*126G= ENSP00000505961.1:n.*126G=
ENST00000681037.1:c.*2517G= ENSP00000506025.1:n.*2517G=
ENST00000681063.1:c.*302G= ENSP00000506616.1:n.*302G=
ENST00000681209.1:c.*688G= ENSP00000505877.1:n.*688G=
ENST00000681278.1:n.1735G=
ENST00000681289.1:n.5028G=
ENST00000681361.1:c.*700G= ENSP00000506679.1:n.*700G=
ENST00000681430.1:c.*126G= ENSP00000506301.1:n.*126G=
ENST00000681446.1:c.*737G= ENSP00000506244.1:n.*737G=
ENST00000681450.1:c.*704G= ENSP00000505660.1:n.*704G=
ENST00000681548.1:c.*619G= ENSP00000505275.1:n.*619G=
ENST00000681616.1:c.*692G= ENSP00000505111.1:n.*692G=
ENST00000681621.1:c.*617G= ENSP00000505770.1:n.*617G=
ENST00000681680.1:n.3128G=
ENST00000681720.1:c.*488G= ENSP00000505438.1:n.*488G=
ENST00000681730.1:n.1255G=
ENST00000681790.1:c.775G= ENSP00000505130.1:p.Asp259=
ENST00000681837.1:n.1649G=
ENST00000681913.1:n.3279G=
ENST00000681916.1:c.*801G= ENSP00000506477.1:n.*801G=
ENST00000681930.1:n.3157G=
ENST00000370834.9:c.1132G= ENSP00000359871.5:p.Asp378=
ENST00000370841.8:c.1033G= ENSP00000359878.4:p.Asp345=
ENST00000420607.6:c.1045G= ENSP00000409612.2:p.Asp349=
ENST00000481374.1:n.306G=
ENST00000525808.5:c.*619G= ENSP00000434823.1:n.*619G=
ENST00000526129.5:c.*817G= ENSP00000434092.1:n.*817G=
ENST00000526196.5:c.*801G= ENSP00000431953.1:n.*801G=
ENST00000528016.1:c.160-7968G= ENSP00000434284.1:n.160-7968G=
ENST00000529059.5:n.942G=
ENST00000534334.5:c.*774G= ENSP00000435584.1:n.*774G=
ENST00000541113.5:c.925G= ENSP00000442324.1:p.Asp309=
NM_000016.5:c.1033G= NP_000007.1:p.Asp345=
NM_001127328.2:c.1045G= NP_001120800.1:p.Asp349=
NM_001286042.1:c.925G= NP_001272971.1:p.Asp309=
NM_001286043.1:c.1132G= NP_001272972.1:p.Asp378=
NM_001286044.1:c.466G= NP_001272973.1:p.Asp156=
NM_000016.6:c.1033G= MANE Select NP_000007.1:p.Asp345=
NM_001127328.3:c.1045G= NP_001120800.1:p.Asp349=
NM_001286042.2:c.925G= NP_001272971.1:p.Asp309=
NM_001286043.2:c.1132G= NP_001272972.1:p.Asp378=
NM_001286044.2:c.466G= NP_001272973.1:p.Asp156=