Canonical Allele Identifier: CA340816928
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750457G>C , CM000663.2:g.75750457G>C GRCh38
NC_000001.10:g.76216142G>C , CM000663.1:g.76216142G>C GRCh37
NC_000001.9:g.75988730G>C NCBI36
NG_007045.2:g.31100G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.856G>C MANE Select ENSP00000359878.5:p.Ala286Pro
ENST00000473018.3:n.2980G>C
ENST00000532207.6:n.1745G>C
ENST00000541113.6:c.849+898G>C ENSP00000442324.2:n.849+898G>C
ENST00000679509.1:n.1818G>C
ENST00000679530.1:c.*624G>C ENSP00000506454.1:n.*624G>C
ENST00000679615.1:n.2871G>C
ENST00000679687.1:c.418G>C ENSP00000506598.1:p.Ala140Pro
ENST00000679704.1:c.*622G>C ENSP00000505117.1:n.*622G>C
ENST00000679709.1:c.*819G>C ENSP00000506623.1:n.*819G>C
ENST00000679976.1:c.*440G>C ENSP00000505565.1:n.*440G>C
ENST00000680166.1:n.4145G>C
ENST00000680315.1:n.739G>C
ENST00000680517.1:c.*244G>C ENSP00000505803.1:n.*244G>C
ENST00000680582.1:n.1818G>C
ENST00000680613.1:c.*227G>C ENSP00000506114.1:n.*227G>C
ENST00000680662.1:c.*770G>C ENSP00000505080.1:n.*770G>C
ENST00000680691.1:c.*519G>C ENSP00000506487.1:n.*519G>C
ENST00000680694.1:c.*444G>C ENSP00000505658.1:n.*444G>C
ENST00000680743.1:c.*523G>C ENSP00000505073.1:n.*523G>C
ENST00000680749.1:c.*141G>C ENSP00000505122.1:n.*141G>C
ENST00000680798.1:c.*331G>C ENSP00000505670.1:n.*331G>C
ENST00000680805.1:c.715G>C ENSP00000505447.1:p.Ala239Pro
ENST00000680844.1:c.*640G>C ENSP00000506541.1:n.*640G>C
ENST00000680948.1:c.*723G>C ENSP00000505441.1:n.*723G>C
ENST00000680964.1:c.856G>C ENSP00000505961.1:p.Ala286Pro
ENST00000681037.1:c.*2340G>C ENSP00000506025.1:n.*2340G>C
ENST00000681063.1:c.*3G>C ENSP00000506616.1:n.*3G>C
ENST00000681209.1:c.*511G>C ENSP00000505877.1:n.*511G>C
ENST00000681278.1:n.1213G>C
ENST00000681289.1:n.4851G>C
ENST00000681361.1:c.*523G>C ENSP00000506679.1:n.*523G>C
ENST00000681430.1:c.856G>C ENSP00000506301.1:p.Ala286Pro
ENST00000681446.1:c.*438G>C ENSP00000506244.1:n.*438G>C
ENST00000681450.1:c.*527G>C ENSP00000505660.1:n.*527G>C
ENST00000681548.1:c.*442G>C ENSP00000505275.1:n.*442G>C
ENST00000681616.1:c.*515G>C ENSP00000505111.1:n.*515G>C
ENST00000681621.1:c.*440G>C ENSP00000505770.1:n.*440G>C
ENST00000681680.1:n.2951G>C
ENST00000681720.1:c.*311G>C ENSP00000505438.1:n.*311G>C
ENST00000681730.1:n.1078G>C
ENST00000681790.1:c.598G>C ENSP00000505130.1:p.Ala200Pro
ENST00000681837.1:n.1472G>C
ENST00000681913.1:n.2980G>C
ENST00000681916.1:c.*624G>C ENSP00000506477.1:n.*624G>C
ENST00000681930.1:n.2980G>C
ENST00000370834.9:c.955G>C ENSP00000359871.5:p.Ala319Pro
ENST00000370841.8:c.856G>C ENSP00000359878.4:p.Ala286Pro
ENST00000420607.6:c.868G>C ENSP00000409612.2:p.Ala290Pro
ENST00000481374.1:n.7G>C
ENST00000525808.5:c.*442G>C ENSP00000434823.1:n.*442G>C
ENST00000526129.5:c.*640G>C ENSP00000434092.1:n.*640G>C
ENST00000526196.5:c.*624G>C ENSP00000431953.1:n.*624G>C
ENST00000528016.1:c.70G>C ENSP00000434284.1:p.Ala24Pro
ENST00000529059.5:n.765G>C
ENST00000532207.5:n.586G>C
ENST00000534334.5:c.*440G>C ENSP00000435584.1:n.*440G>C
ENST00000541113.5:c.748G>C ENSP00000442324.1:p.Ala250Pro
NM_000016.5:c.856G>C NP_000007.1:p.Ala286Pro
NM_001127328.2:c.868G>C NP_001120800.1:p.Ala290Pro
NM_001286042.1:c.748G>C NP_001272971.1:p.Ala250Pro
NM_001286043.1:c.955G>C NP_001272972.1:p.Ala319Pro
NM_001286044.1:c.289G>C NP_001272973.1:p.Ala97Pro
NM_000016.6:c.856G>C MANE Select NP_000007.1:p.Ala286Pro
NM_001127328.3:c.868G>C NP_001120800.1:p.Ala290Pro
NM_001286042.2:c.748G>C NP_001272971.1:p.Ala250Pro
NM_001286043.2:c.955G>C NP_001272972.1:p.Ala319Pro
NM_001286044.2:c.289G>C NP_001272973.1:p.Ala97Pro