Canonical Allele Identifier: CA340816606
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749468A>T , CM000663.2:g.75749468A>T GRCh38
NC_000001.10:g.76215153A>T , CM000663.1:g.76215153A>T GRCh37
NC_000001.9:g.75987741A>T NCBI36
NG_007045.2:g.30111A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.758A>T MANE Select ENSP00000359878.5:p.Glu253Val
ENST00000473018.3:n.2882A>T
ENST00000532207.6:n.1647A>T
ENST00000541113.6:c.758A>T ENSP00000442324.2:p.Glu253Val
ENST00000679509.1:n.1720A>T
ENST00000679530.1:c.*526A>T ENSP00000506454.1:n.*526A>T
ENST00000679615.1:n.2773A>T
ENST00000679687.1:c.320A>T ENSP00000506598.1:p.Glu107Val
ENST00000679704.1:c.*524A>T ENSP00000505117.1:n.*524A>T
ENST00000679709.1:c.*721A>T ENSP00000506623.1:n.*721A>T
ENST00000679976.1:c.*342A>T ENSP00000505565.1:n.*342A>T
ENST00000680166.1:n.4047A>T
ENST00000680517.1:c.*146A>T ENSP00000505803.1:n.*146A>T
ENST00000680582.1:n.1720A>T
ENST00000680613.1:c.*129A>T ENSP00000506114.1:n.*129A>T
ENST00000680662.1:c.*672A>T ENSP00000505080.1:n.*672A>T
ENST00000680691.1:c.*421A>T ENSP00000506487.1:n.*421A>T
ENST00000680694.1:c.*346A>T ENSP00000505658.1:n.*346A>T
ENST00000680743.1:c.*425A>T ENSP00000505073.1:n.*425A>T
ENST00000680749.1:c.*43A>T ENSP00000505122.1:n.*43A>T
ENST00000680798.1:c.*233A>T ENSP00000505670.1:n.*233A>T
ENST00000680805.1:c.709-983A>T ENSP00000505447.1:n.709-983A>T
ENST00000680844.1:c.*542A>T ENSP00000506541.1:n.*542A>T
ENST00000680948.1:c.*625A>T ENSP00000505441.1:n.*625A>T
ENST00000680964.1:c.758A>T ENSP00000505961.1:p.Glu253Val
ENST00000681037.1:c.*2242A>T ENSP00000506025.1:n.*2242A>T
ENST00000681063.1:c.600-983A>T ENSP00000506616.1:n.600-983A>T
ENST00000681209.1:c.*413A>T ENSP00000505877.1:n.*413A>T
ENST00000681278.1:n.1115A>T
ENST00000681289.1:n.4753A>T
ENST00000681361.1:c.*425A>T ENSP00000506679.1:n.*425A>T
ENST00000681430.1:c.758A>T ENSP00000506301.1:p.Glu253Val
ENST00000681446.1:c.*340A>T ENSP00000506244.1:n.*340A>T
ENST00000681450.1:c.*429A>T ENSP00000505660.1:n.*429A>T
ENST00000681548.1:c.*344A>T ENSP00000505275.1:n.*344A>T
ENST00000681616.1:c.*417A>T ENSP00000505111.1:n.*417A>T
ENST00000681621.1:c.*342A>T ENSP00000505770.1:n.*342A>T
ENST00000681680.1:n.2853A>T
ENST00000681720.1:c.*213A>T ENSP00000505438.1:n.*213A>T
ENST00000681730.1:n.980A>T
ENST00000681790.1:c.500A>T ENSP00000505130.1:p.Glu167Val
ENST00000681837.1:n.1374A>T
ENST00000681913.1:n.2882A>T
ENST00000681916.1:c.*526A>T ENSP00000506477.1:n.*526A>T
ENST00000681930.1:n.2882A>T
ENST00000370834.9:c.857A>T ENSP00000359871.5:p.Glu286Val
ENST00000370841.8:c.758A>T ENSP00000359878.4:p.Glu253Val
ENST00000420607.6:c.770A>T ENSP00000409612.2:p.Glu257Val
ENST00000525808.5:c.*344A>T ENSP00000434823.1:n.*344A>T
ENST00000526129.5:c.*542A>T ENSP00000434092.1:n.*542A>T
ENST00000526196.5:c.*526A>T ENSP00000431953.1:n.*526A>T
ENST00000526930.1:n.531A>T
ENST00000529059.5:n.667A>T
ENST00000530953.6:c.*255A>T ENSP00000431372.1:n.*255A>T
ENST00000532207.5:n.488A>T
ENST00000532509.5:c.*522A>T ENSP00000432522.1:n.*522A>T
ENST00000534334.5:c.*342A>T ENSP00000435584.1:n.*342A>T
ENST00000541113.5:c.650A>T ENSP00000442324.1:p.Glu217Val
NM_000016.5:c.758A>T NP_000007.1:p.Glu253Val
NM_001127328.2:c.770A>T NP_001120800.1:p.Glu257Val
NM_001286042.1:c.650A>T NP_001272971.1:p.Glu217Val
NM_001286043.1:c.857A>T NP_001272972.1:p.Glu286Val
NM_001286044.1:c.191A>T NP_001272973.1:p.Glu64Val
NM_000016.6:c.758A>T MANE Select NP_000007.1:p.Glu253Val
NM_001127328.3:c.770A>T NP_001120800.1:p.Glu257Val
NM_001286042.2:c.650A>T NP_001272971.1:p.Glu217Val
NM_001286043.2:c.857A>T NP_001272972.1:p.Glu286Val
NM_001286044.2:c.191A>T NP_001272973.1:p.Glu64Val