Canonical Allele Identifier: CA340817938
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761168A>G , CM000663.2:g.75761168A>G GRCh38
NC_000001.10:g.76226853A>G , CM000663.1:g.76226853A>G GRCh37
NC_000001.9:g.75999441A>G NCBI36
NG_007045.2:g.41811A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.992A>G MANE Select ENSP00000359878.5:p.Glu331Gly
ENST00000473018.3:n.3116A>G
ENST00000532207.6:n.2003A>G
ENST00000541113.6:c.896A>G ENSP00000442324.2:p.Glu299Gly
ENST00000679509.1:n.1954A>G
ENST00000679530.1:c.*760A>G ENSP00000506454.1:n.*760A>G
ENST00000679615.1:n.3007A>G
ENST00000679687.1:c.554A>G ENSP00000506598.1:p.Glu185Gly
ENST00000679704.1:c.*758A>G ENSP00000505117.1:n.*758A>G
ENST00000679709.1:c.*955A>G ENSP00000506623.1:n.*955A>G
ENST00000679976.1:c.*576A>G ENSP00000505565.1:n.*576A>G
ENST00000680166.1:n.4281A>G
ENST00000680315.1:n.875A>G
ENST00000680517.1:c.*380A>G ENSP00000505803.1:n.*380A>G
ENST00000680582.1:n.1954A>G
ENST00000680613.1:c.*485A>G ENSP00000506114.1:n.*485A>G
ENST00000680662.1:c.*906A>G ENSP00000505080.1:n.*906A>G
ENST00000680691.1:c.*655A>G ENSP00000506487.1:n.*655A>G
ENST00000680694.1:c.*580A>G ENSP00000505658.1:n.*580A>G
ENST00000680743.1:c.*781A>G ENSP00000505073.1:n.*781A>G
ENST00000680749.1:c.*277A>G ENSP00000505122.1:n.*277A>G
ENST00000680798.1:c.*467A>G ENSP00000505670.1:n.*467A>G
ENST00000680805.1:c.851A>G ENSP00000505447.1:p.Glu284Gly
ENST00000680844.1:c.*776A>G ENSP00000506541.1:n.*776A>G
ENST00000680948.1:c.*859A>G ENSP00000505441.1:n.*859A>G
ENST00000680964.1:c.*85A>G ENSP00000505961.1:n.*85A>G
ENST00000681037.1:c.*2476A>G ENSP00000506025.1:n.*2476A>G
ENST00000681063.1:c.*261A>G ENSP00000506616.1:n.*261A>G
ENST00000681209.1:c.*647A>G ENSP00000505877.1:n.*647A>G
ENST00000681278.1:n.1694A>G
ENST00000681289.1:n.4987A>G
ENST00000681361.1:c.*659A>G ENSP00000506679.1:n.*659A>G
ENST00000681430.1:c.*85A>G ENSP00000506301.1:n.*85A>G
ENST00000681446.1:c.*696A>G ENSP00000506244.1:n.*696A>G
ENST00000681450.1:c.*663A>G ENSP00000505660.1:n.*663A>G
ENST00000681548.1:c.*578A>G ENSP00000505275.1:n.*578A>G
ENST00000681616.1:c.*651A>G ENSP00000505111.1:n.*651A>G
ENST00000681621.1:c.*576A>G ENSP00000505770.1:n.*576A>G
ENST00000681680.1:n.3087A>G
ENST00000681720.1:c.*447A>G ENSP00000505438.1:n.*447A>G
ENST00000681730.1:n.1214A>G
ENST00000681790.1:c.734A>G ENSP00000505130.1:p.Glu245Gly
ENST00000681837.1:n.1608A>G
ENST00000681913.1:n.3238A>G
ENST00000681916.1:c.*760A>G ENSP00000506477.1:n.*760A>G
ENST00000681930.1:n.3116A>G
ENST00000370834.9:c.1091A>G ENSP00000359871.5:p.Glu364Gly
ENST00000370841.8:c.992A>G ENSP00000359878.4:p.Glu331Gly
ENST00000420607.6:c.1004A>G ENSP00000409612.2:p.Glu335Gly
ENST00000481374.1:n.265A>G
ENST00000525808.5:c.*578A>G ENSP00000434823.1:n.*578A>G
ENST00000526129.5:c.*776A>G ENSP00000434092.1:n.*776A>G
ENST00000526196.5:c.*760A>G ENSP00000431953.1:n.*760A>G
ENST00000528016.1:c.160-8009A>G ENSP00000434284.1:n.160-8009A>G
ENST00000529059.5:n.901A>G
ENST00000532207.5:n.722A>G
ENST00000534334.5:c.*733A>G ENSP00000435584.1:n.*733A>G
ENST00000541113.5:c.884A>G ENSP00000442324.1:p.Glu295Gly
NM_000016.5:c.992A>G NP_000007.1:p.Glu331Gly
NM_001127328.2:c.1004A>G NP_001120800.1:p.Glu335Gly
NM_001286042.1:c.884A>G NP_001272971.1:p.Glu295Gly
NM_001286043.1:c.1091A>G NP_001272972.1:p.Glu364Gly
NM_001286044.1:c.425A>G NP_001272973.1:p.Glu142Gly
NM_000016.6:c.992A>G MANE Select NP_000007.1:p.Glu331Gly
NM_001127328.3:c.1004A>G NP_001120800.1:p.Glu335Gly
NM_001286042.2:c.884A>G NP_001272971.1:p.Glu295Gly
NM_001286043.2:c.1091A>G NP_001272972.1:p.Glu364Gly
NM_001286044.2:c.425A>G NP_001272973.1:p.Glu142Gly