Canonical Allele Identifier: CA340818198
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1114G>C MANE Select ENSP00000359878.5:p.Ala372Pro
ENST00000473018.3:n.3238G>C
ENST00000532207.6:n.2125G>C
ENST00000541113.6:c.1018G>C ENSP00000442324.2:p.Ala340Pro
ENST00000679509.1:n.2076G>C
ENST00000679530.1:c.*882G>C ENSP00000506454.1:n.*882G>C
ENST00000679615.1:n.3129G>C
ENST00000679687.1:c.676G>C ENSP00000506598.1:p.Ala226Pro
ENST00000679704.1:c.*880G>C ENSP00000505117.1:n.*880G>C
ENST00000679709.1:c.*1077G>C ENSP00000506623.1:n.*1077G>C
ENST00000679976.1:c.*698G>C ENSP00000505565.1:n.*698G>C
ENST00000680166.1:n.4403G>C
ENST00000680315.1:n.997G>C
ENST00000680517.1:c.*502G>C ENSP00000505803.1:n.*502G>C
ENST00000680582.1:n.2076G>C
ENST00000680613.1:c.*607G>C ENSP00000506114.1:n.*607G>C
ENST00000680662.1:c.*1028G>C ENSP00000505080.1:n.*1028G>C
ENST00000680691.1:c.*777G>C ENSP00000506487.1:n.*777G>C
ENST00000680694.1:c.*702G>C ENSP00000505658.1:n.*702G>C
ENST00000680743.1:c.*903G>C ENSP00000505073.1:n.*903G>C
ENST00000680749.1:c.*399G>C ENSP00000505122.1:n.*399G>C
ENST00000680798.1:c.*589G>C ENSP00000505670.1:n.*589G>C
ENST00000680805.1:c.973G>C ENSP00000505447.1:p.Ala325Pro
ENST00000680844.1:c.*898G>C ENSP00000506541.1:n.*898G>C
ENST00000680948.1:c.*981G>C ENSP00000505441.1:n.*981G>C
ENST00000680964.1:c.*207G>C ENSP00000505961.1:n.*207G>C
ENST00000681037.1:c.*2598G>C ENSP00000506025.1:n.*2598G>C
ENST00000681063.1:c.*383G>C ENSP00000506616.1:n.*383G>C
ENST00000681209.1:c.*769G>C ENSP00000505877.1:n.*769G>C
ENST00000681278.1:n.1816G>C
ENST00000681289.1:n.5109G>C
ENST00000681361.1:c.*781G>C ENSP00000506679.1:n.*781G>C
ENST00000681430.1:c.*207G>C ENSP00000506301.1:n.*207G>C
ENST00000681446.1:c.*818G>C ENSP00000506244.1:n.*818G>C
ENST00000681450.1:c.*785G>C ENSP00000505660.1:n.*785G>C
ENST00000681548.1:c.*700G>C ENSP00000505275.1:n.*700G>C
ENST00000681616.1:c.*773G>C ENSP00000505111.1:n.*773G>C
ENST00000681621.1:c.*698G>C ENSP00000505770.1:n.*698G>C
ENST00000681680.1:n.3209G>C
ENST00000681720.1:c.*569G>C ENSP00000505438.1:n.*569G>C
ENST00000681730.1:n.1336G>C
ENST00000681790.1:c.856G>C ENSP00000505130.1:p.Ala286Pro
ENST00000681837.1:n.1730G>C
ENST00000681913.1:n.3360G>C
ENST00000681916.1:c.*882G>C ENSP00000506477.1:n.*882G>C
ENST00000681930.1:n.3238G>C
ENST00000370834.9:c.1213G>C ENSP00000359871.5:p.Ala405Pro
ENST00000370841.8:c.1114G>C ENSP00000359878.4:p.Ala372Pro
ENST00000420607.6:c.1126G>C ENSP00000409612.2:p.Ala376Pro
ENST00000481374.1:n.387G>C
ENST00000525808.5:c.*700G>C ENSP00000434823.1:n.*700G>C
ENST00000526129.5:c.*898G>C ENSP00000434092.1:n.*898G>C
ENST00000526196.5:c.*882G>C ENSP00000431953.1:n.*882G>C
ENST00000528016.1:c.160-7887G>C ENSP00000434284.1:n.160-7887G>C
ENST00000529059.5:n.1023G>C
ENST00000541113.5:c.1006G>C ENSP00000442324.1:p.Ala336Pro
NM_000016.5:c.1114G>C NP_000007.1:p.Ala372Pro
NM_001127328.2:c.1126G>C NP_001120800.1:p.Ala376Pro
NM_001286042.1:c.1006G>C NP_001272971.1:p.Ala336Pro
NM_001286043.1:c.1213G>C NP_001272972.1:p.Ala405Pro
NM_001286044.1:c.547G>C NP_001272973.1:p.Ala183Pro
NM_000016.6:c.1114G>C MANE Select NP_000007.1:p.Ala372Pro
NM_001127328.3:c.1126G>C NP_001120800.1:p.Ala376Pro
NM_001286042.2:c.1006G>C NP_001272971.1:p.Ala336Pro
NM_001286043.2:c.1213G>C NP_001272972.1:p.Ala405Pro
NM_001286044.2:c.547G>C NP_001272973.1:p.Ala183Pro