Canonical Allele Identifier: CA340818039
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761213C>G , CM000663.2:g.75761213C>G GRCh38
NC_000001.10:g.76226898C>G , CM000663.1:g.76226898C>G GRCh37
NC_000001.9:g.75999486C>G NCBI36
NG_007045.2:g.41856C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1037C>G MANE Select ENSP00000359878.5:p.Ser346Cys
ENST00000473018.3:n.3161C>G
ENST00000532207.6:n.2048C>G
ENST00000541113.6:c.941C>G ENSP00000442324.2:p.Ser314Cys
ENST00000679509.1:n.1999C>G
ENST00000679530.1:c.*805C>G ENSP00000506454.1:n.*805C>G
ENST00000679615.1:n.3052C>G
ENST00000679687.1:c.599C>G ENSP00000506598.1:p.Ser200Cys
ENST00000679704.1:c.*803C>G ENSP00000505117.1:n.*803C>G
ENST00000679709.1:c.*1000C>G ENSP00000506623.1:n.*1000C>G
ENST00000679976.1:c.*621C>G ENSP00000505565.1:n.*621C>G
ENST00000680166.1:n.4326C>G
ENST00000680315.1:n.920C>G
ENST00000680517.1:c.*425C>G ENSP00000505803.1:n.*425C>G
ENST00000680582.1:n.1999C>G
ENST00000680613.1:c.*530C>G ENSP00000506114.1:n.*530C>G
ENST00000680662.1:c.*951C>G ENSP00000505080.1:n.*951C>G
ENST00000680691.1:c.*700C>G ENSP00000506487.1:n.*700C>G
ENST00000680694.1:c.*625C>G ENSP00000505658.1:n.*625C>G
ENST00000680743.1:c.*826C>G ENSP00000505073.1:n.*826C>G
ENST00000680749.1:c.*322C>G ENSP00000505122.1:n.*322C>G
ENST00000680798.1:c.*512C>G ENSP00000505670.1:n.*512C>G
ENST00000680805.1:c.896C>G ENSP00000505447.1:p.Ser299Cys
ENST00000680844.1:c.*821C>G ENSP00000506541.1:n.*821C>G
ENST00000680948.1:c.*904C>G ENSP00000505441.1:n.*904C>G
ENST00000680964.1:c.*130C>G ENSP00000505961.1:n.*130C>G
ENST00000681037.1:c.*2521C>G ENSP00000506025.1:n.*2521C>G
ENST00000681063.1:c.*306C>G ENSP00000506616.1:n.*306C>G
ENST00000681209.1:c.*692C>G ENSP00000505877.1:n.*692C>G
ENST00000681278.1:n.1739C>G
ENST00000681289.1:n.5032C>G
ENST00000681361.1:c.*704C>G ENSP00000506679.1:n.*704C>G
ENST00000681430.1:c.*130C>G ENSP00000506301.1:n.*130C>G
ENST00000681446.1:c.*741C>G ENSP00000506244.1:n.*741C>G
ENST00000681450.1:c.*708C>G ENSP00000505660.1:n.*708C>G
ENST00000681548.1:c.*623C>G ENSP00000505275.1:n.*623C>G
ENST00000681616.1:c.*696C>G ENSP00000505111.1:n.*696C>G
ENST00000681621.1:c.*621C>G ENSP00000505770.1:n.*621C>G
ENST00000681680.1:n.3132C>G
ENST00000681720.1:c.*492C>G ENSP00000505438.1:n.*492C>G
ENST00000681730.1:n.1259C>G
ENST00000681790.1:c.779C>G ENSP00000505130.1:p.Ser260Cys
ENST00000681837.1:n.1653C>G
ENST00000681913.1:n.3283C>G
ENST00000681916.1:c.*805C>G ENSP00000506477.1:n.*805C>G
ENST00000681930.1:n.3161C>G
ENST00000370834.9:c.1136C>G ENSP00000359871.5:p.Ser379Cys
ENST00000370841.8:c.1037C>G ENSP00000359878.4:p.Ser346Cys
ENST00000420607.6:c.1049C>G ENSP00000409612.2:p.Ser350Cys
ENST00000481374.1:n.310C>G
ENST00000525808.5:c.*623C>G ENSP00000434823.1:n.*623C>G
ENST00000526129.5:c.*821C>G ENSP00000434092.1:n.*821C>G
ENST00000526196.5:c.*805C>G ENSP00000431953.1:n.*805C>G
ENST00000528016.1:c.160-7964C>G ENSP00000434284.1:n.160-7964C>G
ENST00000529059.5:n.946C>G
ENST00000534334.5:c.*778C>G ENSP00000435584.1:n.*778C>G
ENST00000541113.5:c.929C>G ENSP00000442324.1:p.Ser310Cys
NM_000016.5:c.1037C>G NP_000007.1:p.Ser346Cys
NM_001127328.2:c.1049C>G NP_001120800.1:p.Ser350Cys
NM_001286042.1:c.929C>G NP_001272971.1:p.Ser310Cys
NM_001286043.1:c.1136C>G NP_001272972.1:p.Ser379Cys
NM_001286044.1:c.470C>G NP_001272973.1:p.Ser157Cys
NM_000016.6:c.1037C>G MANE Select NP_000007.1:p.Ser346Cys
NM_001127328.3:c.1049C>G NP_001120800.1:p.Ser350Cys
NM_001286042.2:c.929C>G NP_001272971.1:p.Ser310Cys
NM_001286043.2:c.1136C>G NP_001272972.1:p.Ser379Cys
NM_001286044.2:c.470C>G NP_001272973.1:p.Ser157Cys