Canonical Allele Identifier: CA1145495456
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761190G= , CM000663.2:g.75761190G= GRCh38
NC_000001.10:g.76226875G= , CM000663.1:g.76226875G= GRCh37
NC_000001.9:g.75999463G= NCBI36
NG_007045.2:g.41833G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1014G= MANE Select ENSP00000359878.5:p.Gln338=
ENST00000473018.3:n.3138G=
ENST00000532207.6:n.2025G=
ENST00000541113.6:c.918G= ENSP00000442324.2:p.Gln306=
ENST00000679509.1:n.1976G=
ENST00000679530.1:c.*782G= ENSP00000506454.1:n.*782G=
ENST00000679615.1:n.3029G=
ENST00000679687.1:c.576G= ENSP00000506598.1:p.Gln192=
ENST00000679704.1:c.*780G= ENSP00000505117.1:n.*780G=
ENST00000679709.1:c.*977G= ENSP00000506623.1:n.*977G=
ENST00000679976.1:c.*598G= ENSP00000505565.1:n.*598G=
ENST00000680166.1:n.4303G=
ENST00000680315.1:n.897G=
ENST00000680517.1:c.*402G= ENSP00000505803.1:n.*402G=
ENST00000680582.1:n.1976G=
ENST00000680613.1:c.*507G= ENSP00000506114.1:n.*507G=
ENST00000680662.1:c.*928G= ENSP00000505080.1:n.*928G=
ENST00000680691.1:c.*677G= ENSP00000506487.1:n.*677G=
ENST00000680694.1:c.*602G= ENSP00000505658.1:n.*602G=
ENST00000680743.1:c.*803G= ENSP00000505073.1:n.*803G=
ENST00000680749.1:c.*299G= ENSP00000505122.1:n.*299G=
ENST00000680798.1:c.*489G= ENSP00000505670.1:n.*489G=
ENST00000680805.1:c.873G= ENSP00000505447.1:p.Gln291=
ENST00000680844.1:c.*798G= ENSP00000506541.1:n.*798G=
ENST00000680948.1:c.*881G= ENSP00000505441.1:n.*881G=
ENST00000680964.1:c.*107G= ENSP00000505961.1:n.*107G=
ENST00000681037.1:c.*2498G= ENSP00000506025.1:n.*2498G=
ENST00000681063.1:c.*283G= ENSP00000506616.1:n.*283G=
ENST00000681209.1:c.*669G= ENSP00000505877.1:n.*669G=
ENST00000681278.1:n.1716G=
ENST00000681289.1:n.5009G=
ENST00000681361.1:c.*681G= ENSP00000506679.1:n.*681G=
ENST00000681430.1:c.*107G= ENSP00000506301.1:n.*107G=
ENST00000681446.1:c.*718G= ENSP00000506244.1:n.*718G=
ENST00000681450.1:c.*685G= ENSP00000505660.1:n.*685G=
ENST00000681548.1:c.*600G= ENSP00000505275.1:n.*600G=
ENST00000681616.1:c.*673G= ENSP00000505111.1:n.*673G=
ENST00000681621.1:c.*598G= ENSP00000505770.1:n.*598G=
ENST00000681680.1:n.3109G=
ENST00000681720.1:c.*469G= ENSP00000505438.1:n.*469G=
ENST00000681730.1:n.1236G=
ENST00000681790.1:c.756G= ENSP00000505130.1:p.Gln252=
ENST00000681837.1:n.1630G=
ENST00000681913.1:n.3260G=
ENST00000681916.1:c.*782G= ENSP00000506477.1:n.*782G=
ENST00000681930.1:n.3138G=
ENST00000370834.9:c.1113G= ENSP00000359871.5:p.Gln371=
ENST00000370841.8:c.1014G= ENSP00000359878.4:p.Gln338=
ENST00000420607.6:c.1026G= ENSP00000409612.2:p.Gln342=
ENST00000481374.1:n.287G=
ENST00000525808.5:c.*600G= ENSP00000434823.1:n.*600G=
ENST00000526129.5:c.*798G= ENSP00000434092.1:n.*798G=
ENST00000526196.5:c.*782G= ENSP00000431953.1:n.*782G=
ENST00000528016.1:c.160-7987G= ENSP00000434284.1:n.160-7987G=
ENST00000529059.5:n.923G=
ENST00000532207.5:n.744G=
ENST00000534334.5:c.*755G= ENSP00000435584.1:n.*755G=
ENST00000541113.5:c.906G= ENSP00000442324.1:p.Gln302=
NM_000016.5:c.1014G= NP_000007.1:p.Gln338=
NM_001127328.2:c.1026G= NP_001120800.1:p.Gln342=
NM_001286042.1:c.906G= NP_001272971.1:p.Gln302=
NM_001286043.1:c.1113G= NP_001272972.1:p.Gln371=
NM_001286044.1:c.447G= NP_001272973.1:p.Gln149=
NM_000016.6:c.1014G= MANE Select NP_000007.1:p.Gln338=
NM_001127328.3:c.1026G= NP_001120800.1:p.Gln342=
NM_001286042.2:c.906G= NP_001272971.1:p.Gln302=
NM_001286043.2:c.1113G= NP_001272972.1:p.Gln371=
NM_001286044.2:c.447G= NP_001272973.1:p.Gln149=