Canonical Allele Identifier: CA340817908
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761155G>A , CM000663.2:g.75761155G>A GRCh38
NC_000001.10:g.76226840G>A , CM000663.1:g.76226840G>A GRCh37
NC_000001.9:g.75999428G>A NCBI36
NG_007045.2:g.41798G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.979G>A MANE Select ENSP00000359878.5:p.Ala327Thr
ENST00000473018.3:n.3103G>A
ENST00000532207.6:n.1990G>A
ENST00000541113.6:c.883G>A ENSP00000442324.2:p.Ala295Thr
ENST00000679509.1:n.1941G>A
ENST00000679530.1:c.*747G>A ENSP00000506454.1:n.*747G>A
ENST00000679615.1:n.2994G>A
ENST00000679687.1:c.541G>A ENSP00000506598.1:p.Ala181Thr
ENST00000679704.1:c.*745G>A ENSP00000505117.1:n.*745G>A
ENST00000679709.1:c.*942G>A ENSP00000506623.1:n.*942G>A
ENST00000679976.1:c.*563G>A ENSP00000505565.1:n.*563G>A
ENST00000680166.1:n.4268G>A
ENST00000680315.1:n.862G>A
ENST00000680517.1:c.*367G>A ENSP00000505803.1:n.*367G>A
ENST00000680582.1:n.1941G>A
ENST00000680613.1:c.*472G>A ENSP00000506114.1:n.*472G>A
ENST00000680662.1:c.*893G>A ENSP00000505080.1:n.*893G>A
ENST00000680691.1:c.*642G>A ENSP00000506487.1:n.*642G>A
ENST00000680694.1:c.*567G>A ENSP00000505658.1:n.*567G>A
ENST00000680743.1:c.*768G>A ENSP00000505073.1:n.*768G>A
ENST00000680749.1:c.*264G>A ENSP00000505122.1:n.*264G>A
ENST00000680798.1:c.*454G>A ENSP00000505670.1:n.*454G>A
ENST00000680805.1:c.838G>A ENSP00000505447.1:p.Ala280Thr
ENST00000680844.1:c.*763G>A ENSP00000506541.1:n.*763G>A
ENST00000680948.1:c.*846G>A ENSP00000505441.1:n.*846G>A
ENST00000680964.1:c.*72G>A ENSP00000505961.1:n.*72G>A
ENST00000681037.1:c.*2463G>A ENSP00000506025.1:n.*2463G>A
ENST00000681063.1:c.*248G>A ENSP00000506616.1:n.*248G>A
ENST00000681209.1:c.*634G>A ENSP00000505877.1:n.*634G>A
ENST00000681278.1:n.1681G>A
ENST00000681289.1:n.4974G>A
ENST00000681361.1:c.*646G>A ENSP00000506679.1:n.*646G>A
ENST00000681430.1:c.*72G>A ENSP00000506301.1:n.*72G>A
ENST00000681446.1:c.*683G>A ENSP00000506244.1:n.*683G>A
ENST00000681450.1:c.*650G>A ENSP00000505660.1:n.*650G>A
ENST00000681548.1:c.*565G>A ENSP00000505275.1:n.*565G>A
ENST00000681616.1:c.*638G>A ENSP00000505111.1:n.*638G>A
ENST00000681621.1:c.*563G>A ENSP00000505770.1:n.*563G>A
ENST00000681680.1:n.3074G>A
ENST00000681720.1:c.*434G>A ENSP00000505438.1:n.*434G>A
ENST00000681730.1:n.1201G>A
ENST00000681790.1:c.721G>A ENSP00000505130.1:p.Ala241Thr
ENST00000681837.1:n.1595G>A
ENST00000681913.1:n.3225G>A
ENST00000681916.1:c.*747G>A ENSP00000506477.1:n.*747G>A
ENST00000681930.1:n.3103G>A
ENST00000370834.9:c.1078G>A ENSP00000359871.5:p.Ala360Thr
ENST00000370841.8:c.979G>A ENSP00000359878.4:p.Ala327Thr
ENST00000420607.6:c.991G>A ENSP00000409612.2:p.Ala331Thr
ENST00000481374.1:n.252G>A
ENST00000525808.5:c.*565G>A ENSP00000434823.1:n.*565G>A
ENST00000526129.5:c.*763G>A ENSP00000434092.1:n.*763G>A
ENST00000526196.5:c.*747G>A ENSP00000431953.1:n.*747G>A
ENST00000528016.1:c.160-8022G>A ENSP00000434284.1:n.160-8022G>A
ENST00000529059.5:n.888G>A
ENST00000532207.5:n.709G>A
ENST00000534334.5:c.*720G>A ENSP00000435584.1:n.*720G>A
ENST00000541113.5:c.871G>A ENSP00000442324.1:p.Ala291Thr
NM_000016.5:c.979G>A NP_000007.1:p.Ala327Thr
NM_001127328.2:c.991G>A NP_001120800.1:p.Ala331Thr
NM_001286042.1:c.871G>A NP_001272971.1:p.Ala291Thr
NM_001286043.1:c.1078G>A NP_001272972.1:p.Ala360Thr
NM_001286044.1:c.412G>A NP_001272973.1:p.Ala138Thr
NM_000016.6:c.979G>A MANE Select NP_000007.1:p.Ala327Thr
NM_001127328.3:c.991G>A NP_001120800.1:p.Ala331Thr
NM_001286042.2:c.871G>A NP_001272971.1:p.Ala291Thr
NM_001286043.2:c.1078G>A NP_001272972.1:p.Ala360Thr
NM_001286044.2:c.412G>A NP_001272973.1:p.Ala138Thr