Canonical Allele Identifier: CA1176727413
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762726T= , CM000663.2:g.75762726T= GRCh38
NC_000001.10:g.76228411T= , CM000663.1:g.76228411T= GRCh37
NC_000001.9:g.76000999T= NCBI36
NG_007045.2:g.43369T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1229T= MANE Select ENSP00000359878.5:p.Ile410=
ENST00000473018.3:n.3353T=
ENST00000532207.6:n.3561T=
ENST00000541113.6:c.1133T= ENSP00000442324.2:p.Ile378=
ENST00000679509.1:n.3512T=
ENST00000679530.1:c.*997T= ENSP00000506454.1:n.*997T=
ENST00000679615.1:n.4565T=
ENST00000679687.1:c.791T= ENSP00000506598.1:p.Ile264=
ENST00000679704.1:c.*995T= ENSP00000505117.1:n.*995T=
ENST00000679709.1:c.*1192T= ENSP00000506623.1:n.*1192T=
ENST00000679976.1:c.*813T= ENSP00000505565.1:n.*813T=
ENST00000680166.1:n.4518T=
ENST00000680582.1:n.2191T=
ENST00000680613.1:c.*722T= ENSP00000506114.1:n.*722T=
ENST00000680662.1:c.*1143T= ENSP00000505080.1:n.*1143T=
ENST00000680691.1:c.*892T= ENSP00000506487.1:n.*892T=
ENST00000680694.1:c.*817T= ENSP00000505658.1:n.*817T=
ENST00000680743.1:c.*1018T= ENSP00000505073.1:n.*1018T=
ENST00000680749.1:c.*514T= ENSP00000505122.1:n.*514T=
ENST00000680798.1:c.*2025T= ENSP00000505670.1:n.*2025T=
ENST00000680805.1:c.1088T= ENSP00000505447.1:p.Ile363=
ENST00000680844.1:c.*2334T= ENSP00000506541.1:n.*2334T=
ENST00000680948.1:c.*1096T= ENSP00000505441.1:n.*1096T=
ENST00000680964.1:c.*1643T= ENSP00000505961.1:n.*1643T=
ENST00000681037.1:c.*2713T= ENSP00000506025.1:n.*2713T=
ENST00000681063.1:c.*498T= ENSP00000506616.1:n.*498T=
ENST00000681209.1:c.*884T= ENSP00000505877.1:n.*884T=
ENST00000681278.1:n.1931T=
ENST00000681289.1:n.5224T=
ENST00000681361.1:c.*2217T= ENSP00000506679.1:n.*2217T=
ENST00000681430.1:c.*322T= ENSP00000506301.1:n.*322T=
ENST00000681446.1:c.*2254T= ENSP00000506244.1:n.*2254T=
ENST00000681450.1:c.*900T= ENSP00000505660.1:n.*900T=
ENST00000681548.1:c.*2136T= ENSP00000505275.1:n.*2136T=
ENST00000681616.1:c.*2209T= ENSP00000505111.1:n.*2209T=
ENST00000681621.1:c.*2134T= ENSP00000505770.1:n.*2134T=
ENST00000681680.1:n.4645T=
ENST00000681720.1:c.*684T= ENSP00000505438.1:n.*684T=
ENST00000681730.1:n.1451T=
ENST00000681790.1:c.971T= ENSP00000505130.1:p.Ile324=
ENST00000681837.1:n.3166T=
ENST00000681913.1:n.3475T=
ENST00000681916.1:c.*997T= ENSP00000506477.1:n.*997T=
ENST00000681930.1:n.4674T=
ENST00000370834.9:c.1328T= ENSP00000359871.5:p.Ile443=
ENST00000370841.8:c.1229T= ENSP00000359878.4:p.Ile410=
ENST00000420607.6:c.1241T= ENSP00000409612.2:p.Ile414=
ENST00000481374.1:n.468-567T=
ENST00000525808.5:c.*815T= ENSP00000434823.1:n.*815T=
ENST00000526196.5:c.*997T= ENSP00000431953.1:n.*997T=
ENST00000528016.1:c.160-6451T= ENSP00000434284.1:n.160-6451T=
ENST00000529059.5:n.1138T=
ENST00000541113.5:c.1121T= ENSP00000442324.1:p.Ile374=
NM_000016.5:c.1229T= NP_000007.1:p.Ile410=
NM_001127328.2:c.1241T= NP_001120800.1:p.Ile414=
NM_001286042.1:c.1121T= NP_001272971.1:p.Ile374=
NM_001286043.1:c.1328T= NP_001272972.1:p.Ile443=
NM_001286044.1:c.662T= NP_001272973.1:p.Ile221=
NM_000016.6:c.1229T= MANE Select NP_000007.1:p.Ile410=
NM_001127328.3:c.1241T= NP_001120800.1:p.Ile414=
NM_001286042.2:c.1121T= NP_001272971.1:p.Ile374=
NM_001286043.2:c.1328T= NP_001272972.1:p.Ile443=
NM_001286044.2:c.662T= NP_001272973.1:p.Ile221=