Canonical Allele Identifier: CA340818319
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761348T>G , CM000663.2:g.75761348T>G GRCh38
NC_000001.10:g.76227033T>G , CM000663.1:g.76227033T>G GRCh37
NC_000001.9:g.75999621T>G NCBI36
NG_007045.2:g.41991T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1172T>G MANE Select ENSP00000359878.5:p.Met391Arg
ENST00000473018.3:n.3296T>G
ENST00000532207.6:n.2183T>G
ENST00000541113.6:c.1076T>G ENSP00000442324.2:p.Met359Arg
ENST00000679509.1:n.2134T>G
ENST00000679530.1:c.*940T>G ENSP00000506454.1:n.*940T>G
ENST00000679615.1:n.3187T>G
ENST00000679687.1:c.734T>G ENSP00000506598.1:p.Met245Arg
ENST00000679704.1:c.*938T>G ENSP00000505117.1:n.*938T>G
ENST00000679709.1:c.*1135T>G ENSP00000506623.1:n.*1135T>G
ENST00000679976.1:c.*756T>G ENSP00000505565.1:n.*756T>G
ENST00000680166.1:n.4461T>G
ENST00000680315.1:n.1055T>G
ENST00000680517.1:c.*560T>G ENSP00000505803.1:n.*560T>G
ENST00000680582.1:n.2134T>G
ENST00000680613.1:c.*665T>G ENSP00000506114.1:n.*665T>G
ENST00000680662.1:c.*1086T>G ENSP00000505080.1:n.*1086T>G
ENST00000680691.1:c.*835T>G ENSP00000506487.1:n.*835T>G
ENST00000680694.1:c.*760T>G ENSP00000505658.1:n.*760T>G
ENST00000680743.1:c.*961T>G ENSP00000505073.1:n.*961T>G
ENST00000680749.1:c.*457T>G ENSP00000505122.1:n.*457T>G
ENST00000680798.1:c.*647T>G ENSP00000505670.1:n.*647T>G
ENST00000680805.1:c.1031T>G ENSP00000505447.1:p.Met344Arg
ENST00000680844.1:c.*956T>G ENSP00000506541.1:n.*956T>G
ENST00000680948.1:c.*1039T>G ENSP00000505441.1:n.*1039T>G
ENST00000680964.1:c.*265T>G ENSP00000505961.1:n.*265T>G
ENST00000681037.1:c.*2656T>G ENSP00000506025.1:n.*2656T>G
ENST00000681063.1:c.*441T>G ENSP00000506616.1:n.*441T>G
ENST00000681209.1:c.*827T>G ENSP00000505877.1:n.*827T>G
ENST00000681278.1:n.1874T>G
ENST00000681289.1:n.5167T>G
ENST00000681361.1:c.*839T>G ENSP00000506679.1:n.*839T>G
ENST00000681430.1:c.*265T>G ENSP00000506301.1:n.*265T>G
ENST00000681446.1:c.*876T>G ENSP00000506244.1:n.*876T>G
ENST00000681450.1:c.*843T>G ENSP00000505660.1:n.*843T>G
ENST00000681548.1:c.*758T>G ENSP00000505275.1:n.*758T>G
ENST00000681616.1:c.*831T>G ENSP00000505111.1:n.*831T>G
ENST00000681621.1:c.*756T>G ENSP00000505770.1:n.*756T>G
ENST00000681680.1:n.3267T>G
ENST00000681720.1:c.*627T>G ENSP00000505438.1:n.*627T>G
ENST00000681730.1:n.1394T>G
ENST00000681790.1:c.914T>G ENSP00000505130.1:p.Met305Arg
ENST00000681837.1:n.1788T>G
ENST00000681913.1:n.3418T>G
ENST00000681916.1:c.*940T>G ENSP00000506477.1:n.*940T>G
ENST00000681930.1:n.3296T>G
ENST00000370834.9:c.1271T>G ENSP00000359871.5:p.Met424Arg
ENST00000370841.8:c.1172T>G ENSP00000359878.4:p.Met391Arg
ENST00000420607.6:c.1184T>G ENSP00000409612.2:p.Met395Arg
ENST00000481374.1:n.445T>G
ENST00000525808.5:c.*758T>G ENSP00000434823.1:n.*758T>G
ENST00000526129.5:c.*956T>G ENSP00000434092.1:n.*956T>G
ENST00000526196.5:c.*940T>G ENSP00000431953.1:n.*940T>G
ENST00000528016.1:c.160-7829T>G ENSP00000434284.1:n.160-7829T>G
ENST00000529059.5:n.1081T>G
ENST00000541113.5:c.1064T>G ENSP00000442324.1:p.Met355Arg
NM_000016.5:c.1172T>G NP_000007.1:p.Met391Arg
NM_001127328.2:c.1184T>G NP_001120800.1:p.Met395Arg
NM_001286042.1:c.1064T>G NP_001272971.1:p.Met355Arg
NM_001286043.1:c.1271T>G NP_001272972.1:p.Met424Arg
NM_001286044.1:c.605T>G NP_001272973.1:p.Met202Arg
NM_000016.6:c.1172T>G MANE Select NP_000007.1:p.Met391Arg
NM_001127328.3:c.1184T>G NP_001120800.1:p.Met395Arg
NM_001286042.2:c.1064T>G NP_001272971.1:p.Met355Arg
NM_001286043.2:c.1271T>G NP_001272972.1:p.Met424Arg
NM_001286044.2:c.605T>G NP_001272973.1:p.Met202Arg