Canonical Allele Identifier: CA418707732
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76226986A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761301A>T , CM000663.2:g.75761301A>T GRCh38
NC_000001.10:g.76226986A>T , CM000663.1:g.76226986A>T GRCh37
NC_000001.9:g.75999574A>T NCBI36
NG_007045.2:g.41944A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1125A>T MANE Select ENSP00000359878.5:p.Ile375=
ENST00000473018.3:n.3249A>T
ENST00000532207.6:n.2136A>T
ENST00000541113.6:c.1029A>T ENSP00000442324.2:p.Ile343=
ENST00000679509.1:n.2087A>T
ENST00000679530.1:c.*893A>T ENSP00000506454.1:n.*893A>T
ENST00000679615.1:n.3140A>T
ENST00000679687.1:c.687A>T ENSP00000506598.1:p.Ile229=
ENST00000679704.1:c.*891A>T ENSP00000505117.1:n.*891A>T
ENST00000679709.1:c.*1088A>T ENSP00000506623.1:n.*1088A>T
ENST00000679976.1:c.*709A>T ENSP00000505565.1:n.*709A>T
ENST00000680166.1:n.4414A>T
ENST00000680315.1:n.1008A>T
ENST00000680517.1:c.*513A>T ENSP00000505803.1:n.*513A>T
ENST00000680582.1:n.2087A>T
ENST00000680613.1:c.*618A>T ENSP00000506114.1:n.*618A>T
ENST00000680662.1:c.*1039A>T ENSP00000505080.1:n.*1039A>T
ENST00000680691.1:c.*788A>T ENSP00000506487.1:n.*788A>T
ENST00000680694.1:c.*713A>T ENSP00000505658.1:n.*713A>T
ENST00000680743.1:c.*914A>T ENSP00000505073.1:n.*914A>T
ENST00000680749.1:c.*410A>T ENSP00000505122.1:n.*410A>T
ENST00000680798.1:c.*600A>T ENSP00000505670.1:n.*600A>T
ENST00000680805.1:c.984A>T ENSP00000505447.1:p.Ile328=
ENST00000680844.1:c.*909A>T ENSP00000506541.1:n.*909A>T
ENST00000680948.1:c.*992A>T ENSP00000505441.1:n.*992A>T
ENST00000680964.1:c.*218A>T ENSP00000505961.1:n.*218A>T
ENST00000681037.1:c.*2609A>T ENSP00000506025.1:n.*2609A>T
ENST00000681063.1:c.*394A>T ENSP00000506616.1:n.*394A>T
ENST00000681209.1:c.*780A>T ENSP00000505877.1:n.*780A>T
ENST00000681278.1:n.1827A>T
ENST00000681289.1:n.5120A>T
ENST00000681361.1:c.*792A>T ENSP00000506679.1:n.*792A>T
ENST00000681430.1:c.*218A>T ENSP00000506301.1:n.*218A>T
ENST00000681446.1:c.*829A>T ENSP00000506244.1:n.*829A>T
ENST00000681450.1:c.*796A>T ENSP00000505660.1:n.*796A>T
ENST00000681548.1:c.*711A>T ENSP00000505275.1:n.*711A>T
ENST00000681616.1:c.*784A>T ENSP00000505111.1:n.*784A>T
ENST00000681621.1:c.*709A>T ENSP00000505770.1:n.*709A>T
ENST00000681680.1:n.3220A>T
ENST00000681720.1:c.*580A>T ENSP00000505438.1:n.*580A>T
ENST00000681730.1:n.1347A>T
ENST00000681790.1:c.867A>T ENSP00000505130.1:p.Ile289=
ENST00000681837.1:n.1741A>T
ENST00000681913.1:n.3371A>T
ENST00000681916.1:c.*893A>T ENSP00000506477.1:n.*893A>T
ENST00000681930.1:n.3249A>T
ENST00000370834.9:c.1224A>T ENSP00000359871.5:p.Ile408=
ENST00000370841.8:c.1125A>T ENSP00000359878.4:p.Ile375=
ENST00000420607.6:c.1137A>T ENSP00000409612.2:p.Ile379=
ENST00000481374.1:n.398A>T
ENST00000525808.5:c.*711A>T ENSP00000434823.1:n.*711A>T
ENST00000526129.5:c.*909A>T ENSP00000434092.1:n.*909A>T
ENST00000526196.5:c.*893A>T ENSP00000431953.1:n.*893A>T
ENST00000528016.1:c.160-7876A>T ENSP00000434284.1:n.160-7876A>T
ENST00000529059.5:n.1034A>T
ENST00000541113.5:c.1017A>T ENSP00000442324.1:p.Ile339=
NM_000016.5:c.1125A>T NP_000007.1:p.Ile375=
NM_001127328.2:c.1137A>T NP_001120800.1:p.Ile379=
NM_001286042.1:c.1017A>T NP_001272971.1:p.Ile339=
NM_001286043.1:c.1224A>T NP_001272972.1:p.Ile408=
NM_001286044.1:c.558A>T NP_001272973.1:p.Ile186=
NM_000016.6:c.1125A>T MANE Select NP_000007.1:p.Ile375=
NM_001127328.3:c.1137A>T NP_001120800.1:p.Ile379=
NM_001286042.2:c.1017A>T NP_001272971.1:p.Ile339=
NM_001286043.2:c.1224A>T NP_001272972.1:p.Ile408=
NM_001286044.2:c.558A>T NP_001272973.1:p.Ile186=