Canonical Allele Identifier: CA1148448905
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750529G= , CM000663.2:g.75750529G= GRCh38
NC_000001.10:g.76216214G= , CM000663.1:g.76216214G= GRCh37
NC_000001.9:g.75988802G= NCBI36
NG_007045.2:g.31172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.928G= MANE Select ENSP00000359878.5:p.Gly310=
ENST00000473018.3:n.3052G=
ENST00000532207.6:n.1817G=
ENST00000541113.6:c.849+970G= ENSP00000442324.2:n.849+970G=
ENST00000679509.1:n.1890G=
ENST00000679530.1:c.*696G= ENSP00000506454.1:n.*696G=
ENST00000679615.1:n.2943G=
ENST00000679687.1:c.490G= ENSP00000506598.1:p.Gly164=
ENST00000679704.1:c.*694G= ENSP00000505117.1:n.*694G=
ENST00000679709.1:c.*891G= ENSP00000506623.1:n.*891G=
ENST00000679976.1:c.*512G= ENSP00000505565.1:n.*512G=
ENST00000680166.1:n.4217G=
ENST00000680315.1:n.811G=
ENST00000680517.1:c.*316G= ENSP00000505803.1:n.*316G=
ENST00000680582.1:n.1890G=
ENST00000680613.1:c.*299G= ENSP00000506114.1:n.*299G=
ENST00000680662.1:c.*842G= ENSP00000505080.1:n.*842G=
ENST00000680691.1:c.*591G= ENSP00000506487.1:n.*591G=
ENST00000680694.1:c.*516G= ENSP00000505658.1:n.*516G=
ENST00000680743.1:c.*595G= ENSP00000505073.1:n.*595G=
ENST00000680749.1:c.*213G= ENSP00000505122.1:n.*213G=
ENST00000680798.1:c.*403G= ENSP00000505670.1:n.*403G=
ENST00000680805.1:c.787G= ENSP00000505447.1:p.Gly263=
ENST00000680844.1:c.*712G= ENSP00000506541.1:n.*712G=
ENST00000680948.1:c.*795G= ENSP00000505441.1:n.*795G=
ENST00000680964.1:c.928G= ENSP00000505961.1:p.Gly310=
ENST00000681037.1:c.*2412G= ENSP00000506025.1:n.*2412G=
ENST00000681063.1:c.*75G= ENSP00000506616.1:n.*75G=
ENST00000681209.1:c.*583G= ENSP00000505877.1:n.*583G=
ENST00000681278.1:n.1285G=
ENST00000681289.1:n.4923G=
ENST00000681361.1:c.*595G= ENSP00000506679.1:n.*595G=
ENST00000681430.1:c.928G= ENSP00000506301.1:p.Gly310=
ENST00000681446.1:c.*510G= ENSP00000506244.1:n.*510G=
ENST00000681450.1:c.*599G= ENSP00000505660.1:n.*599G=
ENST00000681548.1:c.*514G= ENSP00000505275.1:n.*514G=
ENST00000681616.1:c.*587G= ENSP00000505111.1:n.*587G=
ENST00000681621.1:c.*512G= ENSP00000505770.1:n.*512G=
ENST00000681680.1:n.3023G=
ENST00000681720.1:c.*383G= ENSP00000505438.1:n.*383G=
ENST00000681730.1:n.1150G=
ENST00000681790.1:c.670G= ENSP00000505130.1:p.Gly224=
ENST00000681837.1:n.1544G=
ENST00000681913.1:n.3052G=
ENST00000681916.1:c.*696G= ENSP00000506477.1:n.*696G=
ENST00000681930.1:n.3052G=
ENST00000370834.9:c.1027G= ENSP00000359871.5:p.Gly343=
ENST00000370841.8:c.928G= ENSP00000359878.4:p.Gly310=
ENST00000420607.6:c.940G= ENSP00000409612.2:p.Gly314=
ENST00000481374.1:n.79G=
ENST00000525808.5:c.*514G= ENSP00000434823.1:n.*514G=
ENST00000526129.5:c.*712G= ENSP00000434092.1:n.*712G=
ENST00000526196.5:c.*696G= ENSP00000431953.1:n.*696G=
ENST00000528016.1:c.142G= ENSP00000434284.1:p.Gly48=
ENST00000529059.5:n.837G=
ENST00000532207.5:n.658G=
ENST00000534334.5:c.*512G= ENSP00000435584.1:n.*512G=
ENST00000541113.5:c.820G= ENSP00000442324.1:p.Gly274=
NM_000016.5:c.928G= NP_000007.1:p.Gly310=
NM_001127328.2:c.940G= NP_001120800.1:p.Gly314=
NM_001286042.1:c.820G= NP_001272971.1:p.Gly274=
NM_001286043.1:c.1027G= NP_001272972.1:p.Gly343=
NM_001286044.1:c.361G= NP_001272973.1:p.Gly121=
NM_000016.6:c.928G= MANE Select NP_000007.1:p.Gly310=
NM_001127328.3:c.940G= NP_001120800.1:p.Gly314=
NM_001286042.2:c.820G= NP_001272971.1:p.Gly274=
NM_001286043.2:c.1027G= NP_001272972.1:p.Gly343=
NM_001286044.2:c.361G= NP_001272973.1:p.Gly121=