Canonical Allele Identifier: CA1176726806
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761144T= , CM000663.2:g.75761144T= GRCh38
NC_000001.10:g.76226829T= , CM000663.1:g.76226829T= GRCh37
NC_000001.9:g.75999417T= NCBI36
NG_007045.2:g.41787T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.968T= MANE Select ENSP00000359878.5:p.Leu323=
ENST00000473018.3:n.3092T=
ENST00000532207.6:n.1979T=
ENST00000541113.6:c.872T= ENSP00000442324.2:p.Leu291=
ENST00000679509.1:n.1930T=
ENST00000679530.1:c.*736T= ENSP00000506454.1:n.*736T=
ENST00000679615.1:n.2983T=
ENST00000679687.1:c.530T= ENSP00000506598.1:p.Leu177=
ENST00000679704.1:c.*734T= ENSP00000505117.1:n.*734T=
ENST00000679709.1:c.*931T= ENSP00000506623.1:n.*931T=
ENST00000679976.1:c.*552T= ENSP00000505565.1:n.*552T=
ENST00000680166.1:n.4257T=
ENST00000680315.1:n.851T=
ENST00000680517.1:c.*356T= ENSP00000505803.1:n.*356T=
ENST00000680582.1:n.1930T=
ENST00000680613.1:c.*461T= ENSP00000506114.1:n.*461T=
ENST00000680662.1:c.*882T= ENSP00000505080.1:n.*882T=
ENST00000680691.1:c.*631T= ENSP00000506487.1:n.*631T=
ENST00000680694.1:c.*556T= ENSP00000505658.1:n.*556T=
ENST00000680743.1:c.*757T= ENSP00000505073.1:n.*757T=
ENST00000680749.1:c.*253T= ENSP00000505122.1:n.*253T=
ENST00000680798.1:c.*443T= ENSP00000505670.1:n.*443T=
ENST00000680805.1:c.827T= ENSP00000505447.1:p.Leu276=
ENST00000680844.1:c.*752T= ENSP00000506541.1:n.*752T=
ENST00000680948.1:c.*835T= ENSP00000505441.1:n.*835T=
ENST00000680964.1:c.*61T= ENSP00000505961.1:n.*61T=
ENST00000681037.1:c.*2452T= ENSP00000506025.1:n.*2452T=
ENST00000681063.1:c.*237T= ENSP00000506616.1:n.*237T=
ENST00000681209.1:c.*623T= ENSP00000505877.1:n.*623T=
ENST00000681278.1:n.1670T=
ENST00000681289.1:n.4963T=
ENST00000681361.1:c.*635T= ENSP00000506679.1:n.*635T=
ENST00000681430.1:c.*61T= ENSP00000506301.1:n.*61T=
ENST00000681446.1:c.*672T= ENSP00000506244.1:n.*672T=
ENST00000681450.1:c.*639T= ENSP00000505660.1:n.*639T=
ENST00000681548.1:c.*554T= ENSP00000505275.1:n.*554T=
ENST00000681616.1:c.*627T= ENSP00000505111.1:n.*627T=
ENST00000681621.1:c.*552T= ENSP00000505770.1:n.*552T=
ENST00000681680.1:n.3063T=
ENST00000681720.1:c.*423T= ENSP00000505438.1:n.*423T=
ENST00000681730.1:n.1190T=
ENST00000681790.1:c.710T= ENSP00000505130.1:p.Leu237=
ENST00000681837.1:n.1584T=
ENST00000681913.1:n.3214T=
ENST00000681916.1:c.*736T= ENSP00000506477.1:n.*736T=
ENST00000681930.1:n.3092T=
ENST00000370834.9:c.1067T= ENSP00000359871.5:p.Leu356=
ENST00000370841.8:c.968T= ENSP00000359878.4:p.Leu323=
ENST00000420607.6:c.980T= ENSP00000409612.2:p.Leu327=
ENST00000481374.1:n.241T=
ENST00000525808.5:c.*554T= ENSP00000434823.1:n.*554T=
ENST00000526129.5:c.*752T= ENSP00000434092.1:n.*752T=
ENST00000526196.5:c.*736T= ENSP00000431953.1:n.*736T=
ENST00000528016.1:c.160-8033T= ENSP00000434284.1:n.160-8033T=
ENST00000529059.5:n.877T=
ENST00000532207.5:n.698T=
ENST00000534334.5:c.*709T= ENSP00000435584.1:n.*709T=
ENST00000541113.5:c.860T= ENSP00000442324.1:p.Leu287=
NM_000016.5:c.968T= NP_000007.1:p.Leu323=
NM_001127328.2:c.980T= NP_001120800.1:p.Leu327=
NM_001286042.1:c.860T= NP_001272971.1:p.Leu287=
NM_001286043.1:c.1067T= NP_001272972.1:p.Leu356=
NM_001286044.1:c.401T= NP_001272973.1:p.Leu134=
NM_000016.6:c.968T= MANE Select NP_000007.1:p.Leu323=
NM_001127328.3:c.980T= NP_001120800.1:p.Leu327=
NM_001286042.2:c.860T= NP_001272971.1:p.Leu287=
NM_001286043.2:c.1067T= NP_001272972.1:p.Leu356=
NM_001286044.2:c.401T= NP_001272973.1:p.Leu134=