Canonical Allele Identifier: CA1176726888
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761362A= , CM000663.2:g.75761362A= GRCh38
NC_000001.10:g.76227047A= , CM000663.1:g.76227047A= GRCh37
NC_000001.9:g.75999635A= NCBI36
NG_007045.2:g.42005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1186A= MANE Select ENSP00000359878.5:p.Ile396=
ENST00000473018.3:n.3310A=
ENST00000532207.6:n.2197A=
ENST00000541113.6:c.1090A= ENSP00000442324.2:p.Ile364=
ENST00000679509.1:n.2148A=
ENST00000679530.1:c.*954A= ENSP00000506454.1:n.*954A=
ENST00000679615.1:n.3201A=
ENST00000679687.1:c.748A= ENSP00000506598.1:p.Ile250=
ENST00000679704.1:c.*952A= ENSP00000505117.1:n.*952A=
ENST00000679709.1:c.*1149A= ENSP00000506623.1:n.*1149A=
ENST00000679976.1:c.*770A= ENSP00000505565.1:n.*770A=
ENST00000680166.1:n.4475A=
ENST00000680315.1:n.1069A=
ENST00000680517.1:c.*574A= ENSP00000505803.1:n.*574A=
ENST00000680582.1:n.2148A=
ENST00000680613.1:c.*679A= ENSP00000506114.1:n.*679A=
ENST00000680662.1:c.*1100A= ENSP00000505080.1:n.*1100A=
ENST00000680691.1:c.*849A= ENSP00000506487.1:n.*849A=
ENST00000680694.1:c.*774A= ENSP00000505658.1:n.*774A=
ENST00000680743.1:c.*975A= ENSP00000505073.1:n.*975A=
ENST00000680749.1:c.*471A= ENSP00000505122.1:n.*471A=
ENST00000680798.1:c.*661A= ENSP00000505670.1:n.*661A=
ENST00000680805.1:c.1045A= ENSP00000505447.1:p.Ile349=
ENST00000680844.1:c.*970A= ENSP00000506541.1:n.*970A=
ENST00000680948.1:c.*1053A= ENSP00000505441.1:n.*1053A=
ENST00000680964.1:c.*279A= ENSP00000505961.1:n.*279A=
ENST00000681037.1:c.*2670A= ENSP00000506025.1:n.*2670A=
ENST00000681063.1:c.*455A= ENSP00000506616.1:n.*455A=
ENST00000681209.1:c.*841A= ENSP00000505877.1:n.*841A=
ENST00000681278.1:n.1888A=
ENST00000681289.1:n.5181A=
ENST00000681361.1:c.*853A= ENSP00000506679.1:n.*853A=
ENST00000681430.1:c.*279A= ENSP00000506301.1:n.*279A=
ENST00000681446.1:c.*890A= ENSP00000506244.1:n.*890A=
ENST00000681450.1:c.*857A= ENSP00000505660.1:n.*857A=
ENST00000681548.1:c.*772A= ENSP00000505275.1:n.*772A=
ENST00000681616.1:c.*845A= ENSP00000505111.1:n.*845A=
ENST00000681621.1:c.*770A= ENSP00000505770.1:n.*770A=
ENST00000681680.1:n.3281A=
ENST00000681720.1:c.*641A= ENSP00000505438.1:n.*641A=
ENST00000681730.1:n.1408A=
ENST00000681790.1:c.928A= ENSP00000505130.1:p.Ile310=
ENST00000681837.1:n.1802A=
ENST00000681913.1:n.3432A=
ENST00000681916.1:c.*954A= ENSP00000506477.1:n.*954A=
ENST00000681930.1:n.3310A=
ENST00000370834.9:c.1285A= ENSP00000359871.5:p.Ile429=
ENST00000370841.8:c.1186A= ENSP00000359878.4:p.Ile396=
ENST00000420607.6:c.1198A= ENSP00000409612.2:p.Ile400=
ENST00000481374.1:n.459A=
ENST00000525808.5:c.*772A= ENSP00000434823.1:n.*772A=
ENST00000526129.5:c.*970A= ENSP00000434092.1:n.*970A=
ENST00000526196.5:c.*954A= ENSP00000431953.1:n.*954A=
ENST00000528016.1:c.160-7815A= ENSP00000434284.1:n.160-7815A=
ENST00000529059.5:n.1095A=
ENST00000541113.5:c.1078A= ENSP00000442324.1:p.Ile360=
NM_000016.5:c.1186A= NP_000007.1:p.Ile396=
NM_001127328.2:c.1198A= NP_001120800.1:p.Ile400=
NM_001286042.1:c.1078A= NP_001272971.1:p.Ile360=
NM_001286043.1:c.1285A= NP_001272972.1:p.Ile429=
NM_001286044.1:c.619A= NP_001272973.1:p.Ile207=
NM_000016.6:c.1186A= MANE Select NP_000007.1:p.Ile396=
NM_001127328.3:c.1198A= NP_001120800.1:p.Ile400=
NM_001286042.2:c.1078A= NP_001272971.1:p.Ile360=
NM_001286043.2:c.1285A= NP_001272972.1:p.Ile429=
NM_001286044.2:c.619A= NP_001272973.1:p.Ile207=