Canonical Allele Identifier: CA1176726867
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761290G= , CM000663.2:g.75761290G= GRCh38
NC_000001.10:g.76226975G= , CM000663.1:g.76226975G= GRCh37
NC_000001.9:g.75999563G= NCBI36
NG_007045.2:g.41933G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1114G= MANE Select ENSP00000359878.5:p.Ala372=
ENST00000473018.3:n.3238G=
ENST00000532207.6:n.2125G=
ENST00000541113.6:c.1018G= ENSP00000442324.2:p.Ala340=
ENST00000679509.1:n.2076G=
ENST00000679530.1:c.*882G= ENSP00000506454.1:n.*882G=
ENST00000679615.1:n.3129G=
ENST00000679687.1:c.676G= ENSP00000506598.1:p.Ala226=
ENST00000679704.1:c.*880G= ENSP00000505117.1:n.*880G=
ENST00000679709.1:c.*1077G= ENSP00000506623.1:n.*1077G=
ENST00000679976.1:c.*698G= ENSP00000505565.1:n.*698G=
ENST00000680166.1:n.4403G=
ENST00000680315.1:n.997G=
ENST00000680517.1:c.*502G= ENSP00000505803.1:n.*502G=
ENST00000680582.1:n.2076G=
ENST00000680613.1:c.*607G= ENSP00000506114.1:n.*607G=
ENST00000680662.1:c.*1028G= ENSP00000505080.1:n.*1028G=
ENST00000680691.1:c.*777G= ENSP00000506487.1:n.*777G=
ENST00000680694.1:c.*702G= ENSP00000505658.1:n.*702G=
ENST00000680743.1:c.*903G= ENSP00000505073.1:n.*903G=
ENST00000680749.1:c.*399G= ENSP00000505122.1:n.*399G=
ENST00000680798.1:c.*589G= ENSP00000505670.1:n.*589G=
ENST00000680805.1:c.973G= ENSP00000505447.1:p.Ala325=
ENST00000680844.1:c.*898G= ENSP00000506541.1:n.*898G=
ENST00000680948.1:c.*981G= ENSP00000505441.1:n.*981G=
ENST00000680964.1:c.*207G= ENSP00000505961.1:n.*207G=
ENST00000681037.1:c.*2598G= ENSP00000506025.1:n.*2598G=
ENST00000681063.1:c.*383G= ENSP00000506616.1:n.*383G=
ENST00000681209.1:c.*769G= ENSP00000505877.1:n.*769G=
ENST00000681278.1:n.1816G=
ENST00000681289.1:n.5109G=
ENST00000681361.1:c.*781G= ENSP00000506679.1:n.*781G=
ENST00000681430.1:c.*207G= ENSP00000506301.1:n.*207G=
ENST00000681446.1:c.*818G= ENSP00000506244.1:n.*818G=
ENST00000681450.1:c.*785G= ENSP00000505660.1:n.*785G=
ENST00000681548.1:c.*700G= ENSP00000505275.1:n.*700G=
ENST00000681616.1:c.*773G= ENSP00000505111.1:n.*773G=
ENST00000681621.1:c.*698G= ENSP00000505770.1:n.*698G=
ENST00000681680.1:n.3209G=
ENST00000681720.1:c.*569G= ENSP00000505438.1:n.*569G=
ENST00000681730.1:n.1336G=
ENST00000681790.1:c.856G= ENSP00000505130.1:p.Ala286=
ENST00000681837.1:n.1730G=
ENST00000681913.1:n.3360G=
ENST00000681916.1:c.*882G= ENSP00000506477.1:n.*882G=
ENST00000681930.1:n.3238G=
ENST00000370834.9:c.1213G= ENSP00000359871.5:p.Ala405=
ENST00000370841.8:c.1114G= ENSP00000359878.4:p.Ala372=
ENST00000420607.6:c.1126G= ENSP00000409612.2:p.Ala376=
ENST00000481374.1:n.387G=
ENST00000525808.5:c.*700G= ENSP00000434823.1:n.*700G=
ENST00000526129.5:c.*898G= ENSP00000434092.1:n.*898G=
ENST00000526196.5:c.*882G= ENSP00000431953.1:n.*882G=
ENST00000528016.1:c.160-7887G= ENSP00000434284.1:n.160-7887G=
ENST00000529059.5:n.1023G=
ENST00000541113.5:c.1006G= ENSP00000442324.1:p.Ala336=
NM_000016.5:c.1114G= NP_000007.1:p.Ala372=
NM_001127328.2:c.1126G= NP_001120800.1:p.Ala376=
NM_001286042.1:c.1006G= NP_001272971.1:p.Ala336=
NM_001286043.1:c.1213G= NP_001272972.1:p.Ala405=
NM_001286044.1:c.547G= NP_001272973.1:p.Ala183=
NM_000016.6:c.1114G= MANE Select NP_000007.1:p.Ala372=
NM_001127328.3:c.1126G= NP_001120800.1:p.Ala376=
NM_001286042.2:c.1006G= NP_001272971.1:p.Ala336=
NM_001286043.2:c.1213G= NP_001272972.1:p.Ala405=
NM_001286044.2:c.547G= NP_001272973.1:p.Ala183=