Canonical Allele Identifier: CA1176726826
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761193A= , CM000663.2:g.75761193A= GRCh38
NC_000001.10:g.76226878A= , CM000663.1:g.76226878A= GRCh37
NC_000001.9:g.75999466A= NCBI36
NG_007045.2:g.41836A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1017A= MANE Select ENSP00000359878.5:p.Arg339=
ENST00000473018.3:n.3141A=
ENST00000532207.6:n.2028A=
ENST00000541113.6:c.921A= ENSP00000442324.2:p.Arg307=
ENST00000679509.1:n.1979A=
ENST00000679530.1:c.*785A= ENSP00000506454.1:n.*785A=
ENST00000679615.1:n.3032A=
ENST00000679687.1:c.579A= ENSP00000506598.1:p.Arg193=
ENST00000679704.1:c.*783A= ENSP00000505117.1:n.*783A=
ENST00000679709.1:c.*980A= ENSP00000506623.1:n.*980A=
ENST00000679976.1:c.*601A= ENSP00000505565.1:n.*601A=
ENST00000680166.1:n.4306A=
ENST00000680315.1:n.900A=
ENST00000680517.1:c.*405A= ENSP00000505803.1:n.*405A=
ENST00000680582.1:n.1979A=
ENST00000680613.1:c.*510A= ENSP00000506114.1:n.*510A=
ENST00000680662.1:c.*931A= ENSP00000505080.1:n.*931A=
ENST00000680691.1:c.*680A= ENSP00000506487.1:n.*680A=
ENST00000680694.1:c.*605A= ENSP00000505658.1:n.*605A=
ENST00000680743.1:c.*806A= ENSP00000505073.1:n.*806A=
ENST00000680749.1:c.*302A= ENSP00000505122.1:n.*302A=
ENST00000680798.1:c.*492A= ENSP00000505670.1:n.*492A=
ENST00000680805.1:c.876A= ENSP00000505447.1:p.Arg292=
ENST00000680844.1:c.*801A= ENSP00000506541.1:n.*801A=
ENST00000680948.1:c.*884A= ENSP00000505441.1:n.*884A=
ENST00000680964.1:c.*110A= ENSP00000505961.1:n.*110A=
ENST00000681037.1:c.*2501A= ENSP00000506025.1:n.*2501A=
ENST00000681063.1:c.*286A= ENSP00000506616.1:n.*286A=
ENST00000681209.1:c.*672A= ENSP00000505877.1:n.*672A=
ENST00000681278.1:n.1719A=
ENST00000681289.1:n.5012A=
ENST00000681361.1:c.*684A= ENSP00000506679.1:n.*684A=
ENST00000681430.1:c.*110A= ENSP00000506301.1:n.*110A=
ENST00000681446.1:c.*721A= ENSP00000506244.1:n.*721A=
ENST00000681450.1:c.*688A= ENSP00000505660.1:n.*688A=
ENST00000681548.1:c.*603A= ENSP00000505275.1:n.*603A=
ENST00000681616.1:c.*676A= ENSP00000505111.1:n.*676A=
ENST00000681621.1:c.*601A= ENSP00000505770.1:n.*601A=
ENST00000681680.1:n.3112A=
ENST00000681720.1:c.*472A= ENSP00000505438.1:n.*472A=
ENST00000681730.1:n.1239A=
ENST00000681790.1:c.759A= ENSP00000505130.1:p.Arg253=
ENST00000681837.1:n.1633A=
ENST00000681913.1:n.3263A=
ENST00000681916.1:c.*785A= ENSP00000506477.1:n.*785A=
ENST00000681930.1:n.3141A=
ENST00000370834.9:c.1116A= ENSP00000359871.5:p.Arg372=
ENST00000370841.8:c.1017A= ENSP00000359878.4:p.Arg339=
ENST00000420607.6:c.1029A= ENSP00000409612.2:p.Arg343=
ENST00000481374.1:n.290A=
ENST00000525808.5:c.*603A= ENSP00000434823.1:n.*603A=
ENST00000526129.5:c.*801A= ENSP00000434092.1:n.*801A=
ENST00000526196.5:c.*785A= ENSP00000431953.1:n.*785A=
ENST00000528016.1:c.160-7984A= ENSP00000434284.1:n.160-7984A=
ENST00000529059.5:n.926A=
ENST00000532207.5:n.747A=
ENST00000534334.5:c.*758A= ENSP00000435584.1:n.*758A=
ENST00000541113.5:c.909A= ENSP00000442324.1:p.Arg303=
NM_000016.5:c.1017A= NP_000007.1:p.Arg339=
NM_001127328.2:c.1029A= NP_001120800.1:p.Arg343=
NM_001286042.1:c.909A= NP_001272971.1:p.Arg303=
NM_001286043.1:c.1116A= NP_001272972.1:p.Arg372=
NM_001286044.1:c.450A= NP_001272973.1:p.Arg150=
NM_000016.6:c.1017A= MANE Select NP_000007.1:p.Arg339=
NM_001127328.3:c.1029A= NP_001120800.1:p.Arg343=
NM_001286042.2:c.909A= NP_001272971.1:p.Arg303=
NM_001286043.2:c.1116A= NP_001272972.1:p.Arg372=
NM_001286044.2:c.450A= NP_001272973.1:p.Arg150=