Canonical Allele Identifier: CA340818350
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1186A>C MANE Select ENSP00000359878.5:p.Ile396Leu
ENST00000473018.3:n.3310A>C
ENST00000532207.6:n.2197A>C
ENST00000541113.6:c.1090A>C ENSP00000442324.2:p.Ile364Leu
ENST00000679509.1:n.2148A>C
ENST00000679530.1:c.*954A>C ENSP00000506454.1:n.*954A>C
ENST00000679615.1:n.3201A>C
ENST00000679687.1:c.748A>C ENSP00000506598.1:p.Ile250Leu
ENST00000679704.1:c.*952A>C ENSP00000505117.1:n.*952A>C
ENST00000679709.1:c.*1149A>C ENSP00000506623.1:n.*1149A>C
ENST00000679976.1:c.*770A>C ENSP00000505565.1:n.*770A>C
ENST00000680166.1:n.4475A>C
ENST00000680315.1:n.1069A>C
ENST00000680517.1:c.*574A>C ENSP00000505803.1:n.*574A>C
ENST00000680582.1:n.2148A>C
ENST00000680613.1:c.*679A>C ENSP00000506114.1:n.*679A>C
ENST00000680662.1:c.*1100A>C ENSP00000505080.1:n.*1100A>C
ENST00000680691.1:c.*849A>C ENSP00000506487.1:n.*849A>C
ENST00000680694.1:c.*774A>C ENSP00000505658.1:n.*774A>C
ENST00000680743.1:c.*975A>C ENSP00000505073.1:n.*975A>C
ENST00000680749.1:c.*471A>C ENSP00000505122.1:n.*471A>C
ENST00000680798.1:c.*661A>C ENSP00000505670.1:n.*661A>C
ENST00000680805.1:c.1045A>C ENSP00000505447.1:p.Ile349Leu
ENST00000680844.1:c.*970A>C ENSP00000506541.1:n.*970A>C
ENST00000680948.1:c.*1053A>C ENSP00000505441.1:n.*1053A>C
ENST00000680964.1:c.*279A>C ENSP00000505961.1:n.*279A>C
ENST00000681037.1:c.*2670A>C ENSP00000506025.1:n.*2670A>C
ENST00000681063.1:c.*455A>C ENSP00000506616.1:n.*455A>C
ENST00000681209.1:c.*841A>C ENSP00000505877.1:n.*841A>C
ENST00000681278.1:n.1888A>C
ENST00000681289.1:n.5181A>C
ENST00000681361.1:c.*853A>C ENSP00000506679.1:n.*853A>C
ENST00000681430.1:c.*279A>C ENSP00000506301.1:n.*279A>C
ENST00000681446.1:c.*890A>C ENSP00000506244.1:n.*890A>C
ENST00000681450.1:c.*857A>C ENSP00000505660.1:n.*857A>C
ENST00000681548.1:c.*772A>C ENSP00000505275.1:n.*772A>C
ENST00000681616.1:c.*845A>C ENSP00000505111.1:n.*845A>C
ENST00000681621.1:c.*770A>C ENSP00000505770.1:n.*770A>C
ENST00000681680.1:n.3281A>C
ENST00000681720.1:c.*641A>C ENSP00000505438.1:n.*641A>C
ENST00000681730.1:n.1408A>C
ENST00000681790.1:c.928A>C ENSP00000505130.1:p.Ile310Leu
ENST00000681837.1:n.1802A>C
ENST00000681913.1:n.3432A>C
ENST00000681916.1:c.*954A>C ENSP00000506477.1:n.*954A>C
ENST00000681930.1:n.3310A>C
ENST00000370834.9:c.1285A>C ENSP00000359871.5:p.Ile429Leu
ENST00000370841.8:c.1186A>C ENSP00000359878.4:p.Ile396Leu
ENST00000420607.6:c.1198A>C ENSP00000409612.2:p.Ile400Leu
ENST00000481374.1:n.459A>C
ENST00000525808.5:c.*772A>C ENSP00000434823.1:n.*772A>C
ENST00000526129.5:c.*970A>C ENSP00000434092.1:n.*970A>C
ENST00000526196.5:c.*954A>C ENSP00000431953.1:n.*954A>C
ENST00000528016.1:c.160-7815A>C ENSP00000434284.1:n.160-7815A>C
ENST00000529059.5:n.1095A>C
ENST00000541113.5:c.1078A>C ENSP00000442324.1:p.Ile360Leu
NM_000016.5:c.1186A>C NP_000007.1:p.Ile396Leu
NM_001127328.2:c.1198A>C NP_001120800.1:p.Ile400Leu
NM_001286042.1:c.1078A>C NP_001272971.1:p.Ile360Leu
NM_001286043.1:c.1285A>C NP_001272972.1:p.Ile429Leu
NM_001286044.1:c.619A>C NP_001272973.1:p.Ile207Leu
NM_000016.6:c.1186A>C MANE Select NP_000007.1:p.Ile396Leu
NM_001127328.3:c.1198A>C NP_001120800.1:p.Ile400Leu
NM_001286042.2:c.1078A>C NP_001272971.1:p.Ile360Leu
NM_001286043.2:c.1285A>C NP_001272972.1:p.Ile429Leu
NM_001286044.2:c.619A>C NP_001272973.1:p.Ile207Leu