Canonical Allele Identifier: CA340818226
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761305G>C , CM000663.2:g.75761305G>C GRCh38
NC_000001.10:g.76226990G>C , CM000663.1:g.76226990G>C GRCh37
NC_000001.9:g.75999578G>C NCBI36
NG_007045.2:g.41948G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1129G>C MANE Select ENSP00000359878.5:p.Gly377Arg
ENST00000473018.3:n.3253G>C
ENST00000532207.6:n.2140G>C
ENST00000541113.6:c.1033G>C ENSP00000442324.2:p.Gly345Arg
ENST00000679509.1:n.2091G>C
ENST00000679530.1:c.*897G>C ENSP00000506454.1:n.*897G>C
ENST00000679615.1:n.3144G>C
ENST00000679687.1:c.691G>C ENSP00000506598.1:p.Gly231Arg
ENST00000679704.1:c.*895G>C ENSP00000505117.1:n.*895G>C
ENST00000679709.1:c.*1092G>C ENSP00000506623.1:n.*1092G>C
ENST00000679976.1:c.*713G>C ENSP00000505565.1:n.*713G>C
ENST00000680166.1:n.4418G>C
ENST00000680315.1:n.1012G>C
ENST00000680517.1:c.*517G>C ENSP00000505803.1:n.*517G>C
ENST00000680582.1:n.2091G>C
ENST00000680613.1:c.*622G>C ENSP00000506114.1:n.*622G>C
ENST00000680662.1:c.*1043G>C ENSP00000505080.1:n.*1043G>C
ENST00000680691.1:c.*792G>C ENSP00000506487.1:n.*792G>C
ENST00000680694.1:c.*717G>C ENSP00000505658.1:n.*717G>C
ENST00000680743.1:c.*918G>C ENSP00000505073.1:n.*918G>C
ENST00000680749.1:c.*414G>C ENSP00000505122.1:n.*414G>C
ENST00000680798.1:c.*604G>C ENSP00000505670.1:n.*604G>C
ENST00000680805.1:c.988G>C ENSP00000505447.1:p.Gly330Arg
ENST00000680844.1:c.*913G>C ENSP00000506541.1:n.*913G>C
ENST00000680948.1:c.*996G>C ENSP00000505441.1:n.*996G>C
ENST00000680964.1:c.*222G>C ENSP00000505961.1:n.*222G>C
ENST00000681037.1:c.*2613G>C ENSP00000506025.1:n.*2613G>C
ENST00000681063.1:c.*398G>C ENSP00000506616.1:n.*398G>C
ENST00000681209.1:c.*784G>C ENSP00000505877.1:n.*784G>C
ENST00000681278.1:n.1831G>C
ENST00000681289.1:n.5124G>C
ENST00000681361.1:c.*796G>C ENSP00000506679.1:n.*796G>C
ENST00000681430.1:c.*222G>C ENSP00000506301.1:n.*222G>C
ENST00000681446.1:c.*833G>C ENSP00000506244.1:n.*833G>C
ENST00000681450.1:c.*800G>C ENSP00000505660.1:n.*800G>C
ENST00000681548.1:c.*715G>C ENSP00000505275.1:n.*715G>C
ENST00000681616.1:c.*788G>C ENSP00000505111.1:n.*788G>C
ENST00000681621.1:c.*713G>C ENSP00000505770.1:n.*713G>C
ENST00000681680.1:n.3224G>C
ENST00000681720.1:c.*584G>C ENSP00000505438.1:n.*584G>C
ENST00000681730.1:n.1351G>C
ENST00000681790.1:c.871G>C ENSP00000505130.1:p.Gly291Arg
ENST00000681837.1:n.1745G>C
ENST00000681913.1:n.3375G>C
ENST00000681916.1:c.*897G>C ENSP00000506477.1:n.*897G>C
ENST00000681930.1:n.3253G>C
ENST00000370834.9:c.1228G>C ENSP00000359871.5:p.Gly410Arg
ENST00000370841.8:c.1129G>C ENSP00000359878.4:p.Gly377Arg
ENST00000420607.6:c.1141G>C ENSP00000409612.2:p.Gly381Arg
ENST00000481374.1:n.402G>C
ENST00000525808.5:c.*715G>C ENSP00000434823.1:n.*715G>C
ENST00000526129.5:c.*913G>C ENSP00000434092.1:n.*913G>C
ENST00000526196.5:c.*897G>C ENSP00000431953.1:n.*897G>C
ENST00000528016.1:c.160-7872G>C ENSP00000434284.1:n.160-7872G>C
ENST00000529059.5:n.1038G>C
ENST00000541113.5:c.1021G>C ENSP00000442324.1:p.Gly341Arg
NM_000016.5:c.1129G>C NP_000007.1:p.Gly377Arg
NM_001127328.2:c.1141G>C NP_001120800.1:p.Gly381Arg
NM_001286042.1:c.1021G>C NP_001272971.1:p.Gly341Arg
NM_001286043.1:c.1228G>C NP_001272972.1:p.Gly410Arg
NM_001286044.1:c.562G>C NP_001272973.1:p.Gly188Arg
NM_000016.6:c.1129G>C MANE Select NP_000007.1:p.Gly377Arg
NM_001127328.3:c.1141G>C NP_001120800.1:p.Gly381Arg
NM_001286042.2:c.1021G>C NP_001272971.1:p.Gly341Arg
NM_001286043.2:c.1228G>C NP_001272972.1:p.Gly410Arg
NM_001286044.2:c.562G>C NP_001272973.1:p.Gly188Arg