Canonical Allele Identifier: CA1176726837
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761216G= , CM000663.2:g.75761216G= GRCh38
NC_000001.10:g.76226901G= , CM000663.1:g.76226901G= GRCh37
NC_000001.9:g.75999489G= NCBI36
NG_007045.2:g.41859G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1040G= MANE Select ENSP00000359878.5:p.Gly347=
ENST00000473018.3:n.3164G=
ENST00000532207.6:n.2051G=
ENST00000541113.6:c.944G= ENSP00000442324.2:p.Gly315=
ENST00000679509.1:n.2002G=
ENST00000679530.1:c.*808G= ENSP00000506454.1:n.*808G=
ENST00000679615.1:n.3055G=
ENST00000679687.1:c.602G= ENSP00000506598.1:p.Gly201=
ENST00000679704.1:c.*806G= ENSP00000505117.1:n.*806G=
ENST00000679709.1:c.*1003G= ENSP00000506623.1:n.*1003G=
ENST00000679976.1:c.*624G= ENSP00000505565.1:n.*624G=
ENST00000680166.1:n.4329G=
ENST00000680315.1:n.923G=
ENST00000680517.1:c.*428G= ENSP00000505803.1:n.*428G=
ENST00000680582.1:n.2002G=
ENST00000680613.1:c.*533G= ENSP00000506114.1:n.*533G=
ENST00000680662.1:c.*954G= ENSP00000505080.1:n.*954G=
ENST00000680691.1:c.*703G= ENSP00000506487.1:n.*703G=
ENST00000680694.1:c.*628G= ENSP00000505658.1:n.*628G=
ENST00000680743.1:c.*829G= ENSP00000505073.1:n.*829G=
ENST00000680749.1:c.*325G= ENSP00000505122.1:n.*325G=
ENST00000680798.1:c.*515G= ENSP00000505670.1:n.*515G=
ENST00000680805.1:c.899G= ENSP00000505447.1:p.Gly300=
ENST00000680844.1:c.*824G= ENSP00000506541.1:n.*824G=
ENST00000680948.1:c.*907G= ENSP00000505441.1:n.*907G=
ENST00000680964.1:c.*133G= ENSP00000505961.1:n.*133G=
ENST00000681037.1:c.*2524G= ENSP00000506025.1:n.*2524G=
ENST00000681063.1:c.*309G= ENSP00000506616.1:n.*309G=
ENST00000681209.1:c.*695G= ENSP00000505877.1:n.*695G=
ENST00000681278.1:n.1742G=
ENST00000681289.1:n.5035G=
ENST00000681361.1:c.*707G= ENSP00000506679.1:n.*707G=
ENST00000681430.1:c.*133G= ENSP00000506301.1:n.*133G=
ENST00000681446.1:c.*744G= ENSP00000506244.1:n.*744G=
ENST00000681450.1:c.*711G= ENSP00000505660.1:n.*711G=
ENST00000681548.1:c.*626G= ENSP00000505275.1:n.*626G=
ENST00000681616.1:c.*699G= ENSP00000505111.1:n.*699G=
ENST00000681621.1:c.*624G= ENSP00000505770.1:n.*624G=
ENST00000681680.1:n.3135G=
ENST00000681720.1:c.*495G= ENSP00000505438.1:n.*495G=
ENST00000681730.1:n.1262G=
ENST00000681790.1:c.782G= ENSP00000505130.1:p.Gly261=
ENST00000681837.1:n.1656G=
ENST00000681913.1:n.3286G=
ENST00000681916.1:c.*808G= ENSP00000506477.1:n.*808G=
ENST00000681930.1:n.3164G=
ENST00000370834.9:c.1139G= ENSP00000359871.5:p.Gly380=
ENST00000370841.8:c.1040G= ENSP00000359878.4:p.Gly347=
ENST00000420607.6:c.1052G= ENSP00000409612.2:p.Gly351=
ENST00000481374.1:n.313G=
ENST00000525808.5:c.*626G= ENSP00000434823.1:n.*626G=
ENST00000526129.5:c.*824G= ENSP00000434092.1:n.*824G=
ENST00000526196.5:c.*808G= ENSP00000431953.1:n.*808G=
ENST00000528016.1:c.160-7961G= ENSP00000434284.1:n.160-7961G=
ENST00000529059.5:n.949G=
ENST00000534334.5:c.*781G= ENSP00000435584.1:n.*781G=
ENST00000541113.5:c.932G= ENSP00000442324.1:p.Gly311=
NM_000016.5:c.1040G= NP_000007.1:p.Gly347=
NM_001127328.2:c.1052G= NP_001120800.1:p.Gly351=
NM_001286042.1:c.932G= NP_001272971.1:p.Gly311=
NM_001286043.1:c.1139G= NP_001272972.1:p.Gly380=
NM_001286044.1:c.473G= NP_001272973.1:p.Gly158=
NM_000016.6:c.1040G= MANE Select NP_000007.1:p.Gly347=
NM_001127328.3:c.1052G= NP_001120800.1:p.Gly351=
NM_001286042.2:c.932G= NP_001272971.1:p.Gly311=
NM_001286043.2:c.1139G= NP_001272972.1:p.Gly380=
NM_001286044.2:c.473G= NP_001272973.1:p.Gly158=