Canonical Allele Identifier: CA340818441
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762717A>G , CM000663.2:g.75762717A>G GRCh38
NC_000001.10:g.76228402A>G , CM000663.1:g.76228402A>G GRCh37
NC_000001.9:g.76000990A>G NCBI36
NG_007045.2:g.43360A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1220A>G MANE Select ENSP00000359878.5:p.Gln407Arg
ENST00000473018.3:n.3344A>G
ENST00000532207.6:n.3552A>G
ENST00000541113.6:c.1124A>G ENSP00000442324.2:p.Gln375Arg
ENST00000679509.1:n.3503A>G
ENST00000679530.1:c.*988A>G ENSP00000506454.1:n.*988A>G
ENST00000679615.1:n.4556A>G
ENST00000679687.1:c.782A>G ENSP00000506598.1:p.Gln261Arg
ENST00000679704.1:c.*986A>G ENSP00000505117.1:n.*986A>G
ENST00000679709.1:c.*1183A>G ENSP00000506623.1:n.*1183A>G
ENST00000679976.1:c.*804A>G ENSP00000505565.1:n.*804A>G
ENST00000680166.1:n.4509A>G
ENST00000680517.1:c.*1929A>G ENSP00000505803.1:n.*1929A>G
ENST00000680582.1:n.2182A>G
ENST00000680613.1:c.*713A>G ENSP00000506114.1:n.*713A>G
ENST00000680662.1:c.*1134A>G ENSP00000505080.1:n.*1134A>G
ENST00000680691.1:c.*883A>G ENSP00000506487.1:n.*883A>G
ENST00000680694.1:c.*808A>G ENSP00000505658.1:n.*808A>G
ENST00000680743.1:c.*1009A>G ENSP00000505073.1:n.*1009A>G
ENST00000680749.1:c.*505A>G ENSP00000505122.1:n.*505A>G
ENST00000680798.1:c.*2016A>G ENSP00000505670.1:n.*2016A>G
ENST00000680805.1:c.1079A>G ENSP00000505447.1:p.Gln360Arg
ENST00000680844.1:c.*2325A>G ENSP00000506541.1:n.*2325A>G
ENST00000680948.1:c.*1087A>G ENSP00000505441.1:n.*1087A>G
ENST00000680964.1:c.*1634A>G ENSP00000505961.1:n.*1634A>G
ENST00000681037.1:c.*2704A>G ENSP00000506025.1:n.*2704A>G
ENST00000681063.1:c.*489A>G ENSP00000506616.1:n.*489A>G
ENST00000681209.1:c.*875A>G ENSP00000505877.1:n.*875A>G
ENST00000681278.1:n.1922A>G
ENST00000681289.1:n.5215A>G
ENST00000681361.1:c.*2208A>G ENSP00000506679.1:n.*2208A>G
ENST00000681430.1:c.*313A>G ENSP00000506301.1:n.*313A>G
ENST00000681446.1:c.*2245A>G ENSP00000506244.1:n.*2245A>G
ENST00000681450.1:c.*891A>G ENSP00000505660.1:n.*891A>G
ENST00000681548.1:c.*2127A>G ENSP00000505275.1:n.*2127A>G
ENST00000681616.1:c.*2200A>G ENSP00000505111.1:n.*2200A>G
ENST00000681621.1:c.*2125A>G ENSP00000505770.1:n.*2125A>G
ENST00000681680.1:n.4636A>G
ENST00000681720.1:c.*675A>G ENSP00000505438.1:n.*675A>G
ENST00000681730.1:n.1442A>G
ENST00000681790.1:c.962A>G ENSP00000505130.1:p.Gln321Arg
ENST00000681837.1:n.3157A>G
ENST00000681913.1:n.3466A>G
ENST00000681916.1:c.*988A>G ENSP00000506477.1:n.*988A>G
ENST00000681930.1:n.4665A>G
ENST00000370834.9:c.1319A>G ENSP00000359871.5:p.Gln440Arg
ENST00000370841.8:c.1220A>G ENSP00000359878.4:p.Gln407Arg
ENST00000420607.6:c.1232A>G ENSP00000409612.2:p.Gln411Arg
ENST00000481374.1:n.468-576A>G
ENST00000525808.5:c.*806A>G ENSP00000434823.1:n.*806A>G
ENST00000526196.5:c.*988A>G ENSP00000431953.1:n.*988A>G
ENST00000528016.1:c.160-6460A>G ENSP00000434284.1:n.160-6460A>G
ENST00000529059.5:n.1129A>G
ENST00000541113.5:c.1112A>G ENSP00000442324.1:p.Gln371Arg
NM_000016.5:c.1220A>G NP_000007.1:p.Gln407Arg
NM_001127328.2:c.1232A>G NP_001120800.1:p.Gln411Arg
NM_001286042.1:c.1112A>G NP_001272971.1:p.Gln371Arg
NM_001286043.1:c.1319A>G NP_001272972.1:p.Gln440Arg
NM_001286044.1:c.653A>G NP_001272973.1:p.Gln218Arg
NM_000016.6:c.1220A>G MANE Select NP_000007.1:p.Gln407Arg
NM_001127328.3:c.1232A>G NP_001120800.1:p.Gln411Arg
NM_001286042.2:c.1112A>G NP_001272971.1:p.Gln371Arg
NM_001286043.2:c.1319A>G NP_001272972.1:p.Gln440Arg
NM_001286044.2:c.653A>G NP_001272973.1:p.Gln218Arg