Canonical Allele Identifier: CA1176721857
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750466G= , CM000663.2:g.75750466G= GRCh38
NC_000001.10:g.76216151G= , CM000663.1:g.76216151G= GRCh37
NC_000001.9:g.75988739G= NCBI36
NG_007045.2:g.31109G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.865G= MANE Select ENSP00000359878.5:p.Val289=
ENST00000473018.3:n.2989G=
ENST00000532207.6:n.1754G=
ENST00000541113.6:c.849+907G= ENSP00000442324.2:n.849+907G=
ENST00000679509.1:n.1827G=
ENST00000679530.1:c.*633G= ENSP00000506454.1:n.*633G=
ENST00000679615.1:n.2880G=
ENST00000679687.1:c.427G= ENSP00000506598.1:p.Val143=
ENST00000679704.1:c.*631G= ENSP00000505117.1:n.*631G=
ENST00000679709.1:c.*828G= ENSP00000506623.1:n.*828G=
ENST00000679976.1:c.*449G= ENSP00000505565.1:n.*449G=
ENST00000680166.1:n.4154G=
ENST00000680315.1:n.748G=
ENST00000680517.1:c.*253G= ENSP00000505803.1:n.*253G=
ENST00000680582.1:n.1827G=
ENST00000680613.1:c.*236G= ENSP00000506114.1:n.*236G=
ENST00000680662.1:c.*779G= ENSP00000505080.1:n.*779G=
ENST00000680691.1:c.*528G= ENSP00000506487.1:n.*528G=
ENST00000680694.1:c.*453G= ENSP00000505658.1:n.*453G=
ENST00000680743.1:c.*532G= ENSP00000505073.1:n.*532G=
ENST00000680749.1:c.*150G= ENSP00000505122.1:n.*150G=
ENST00000680798.1:c.*340G= ENSP00000505670.1:n.*340G=
ENST00000680805.1:c.724G= ENSP00000505447.1:p.Val242=
ENST00000680844.1:c.*649G= ENSP00000506541.1:n.*649G=
ENST00000680948.1:c.*732G= ENSP00000505441.1:n.*732G=
ENST00000680964.1:c.865G= ENSP00000505961.1:p.Val289=
ENST00000681037.1:c.*2349G= ENSP00000506025.1:n.*2349G=
ENST00000681063.1:c.*12G= ENSP00000506616.1:n.*12G=
ENST00000681209.1:c.*520G= ENSP00000505877.1:n.*520G=
ENST00000681278.1:n.1222G=
ENST00000681289.1:n.4860G=
ENST00000681361.1:c.*532G= ENSP00000506679.1:n.*532G=
ENST00000681430.1:c.865G= ENSP00000506301.1:p.Val289=
ENST00000681446.1:c.*447G= ENSP00000506244.1:n.*447G=
ENST00000681450.1:c.*536G= ENSP00000505660.1:n.*536G=
ENST00000681548.1:c.*451G= ENSP00000505275.1:n.*451G=
ENST00000681616.1:c.*524G= ENSP00000505111.1:n.*524G=
ENST00000681621.1:c.*449G= ENSP00000505770.1:n.*449G=
ENST00000681680.1:n.2960G=
ENST00000681720.1:c.*320G= ENSP00000505438.1:n.*320G=
ENST00000681730.1:n.1087G=
ENST00000681790.1:c.607G= ENSP00000505130.1:p.Val203=
ENST00000681837.1:n.1481G=
ENST00000681913.1:n.2989G=
ENST00000681916.1:c.*633G= ENSP00000506477.1:n.*633G=
ENST00000681930.1:n.2989G=
ENST00000370834.9:c.964G= ENSP00000359871.5:p.Val322=
ENST00000370841.8:c.865G= ENSP00000359878.4:p.Val289=
ENST00000420607.6:c.877G= ENSP00000409612.2:p.Val293=
ENST00000481374.1:n.16G=
ENST00000525808.5:c.*451G= ENSP00000434823.1:n.*451G=
ENST00000526129.5:c.*649G= ENSP00000434092.1:n.*649G=
ENST00000526196.5:c.*633G= ENSP00000431953.1:n.*633G=
ENST00000528016.1:c.79G= ENSP00000434284.1:p.Val27=
ENST00000529059.5:n.774G=
ENST00000532207.5:n.595G=
ENST00000534334.5:c.*449G= ENSP00000435584.1:n.*449G=
ENST00000541113.5:c.757G= ENSP00000442324.1:p.Val253=
NM_000016.5:c.865G= NP_000007.1:p.Val289=
NM_001127328.2:c.877G= NP_001120800.1:p.Val293=
NM_001286042.1:c.757G= NP_001272971.1:p.Val253=
NM_001286043.1:c.964G= NP_001272972.1:p.Val322=
NM_001286044.1:c.298G= NP_001272973.1:p.Val100=
NM_000016.6:c.865G= MANE Select NP_000007.1:p.Val289=
NM_001127328.3:c.877G= NP_001120800.1:p.Val293=
NM_001286042.2:c.757G= NP_001272971.1:p.Val253=
NM_001286043.2:c.964G= NP_001272972.1:p.Val322=
NM_001286044.2:c.298G= NP_001272973.1:p.Val100=