Canonical Allele Identifier: CA340817928
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761164G>A , CM000663.2:g.75761164G>A GRCh38
NC_000001.10:g.76226849G>A , CM000663.1:g.76226849G>A GRCh37
NC_000001.9:g.75999437G>A NCBI36
NG_007045.2:g.41807G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.988G>A MANE Select ENSP00000359878.5:p.Val330Ile
ENST00000473018.3:n.3112G>A
ENST00000532207.6:n.1999G>A
ENST00000541113.6:c.892G>A ENSP00000442324.2:p.Val298Ile
ENST00000679509.1:n.1950G>A
ENST00000679530.1:c.*756G>A ENSP00000506454.1:n.*756G>A
ENST00000679615.1:n.3003G>A
ENST00000679687.1:c.550G>A ENSP00000506598.1:p.Val184Ile
ENST00000679704.1:c.*754G>A ENSP00000505117.1:n.*754G>A
ENST00000679709.1:c.*951G>A ENSP00000506623.1:n.*951G>A
ENST00000679976.1:c.*572G>A ENSP00000505565.1:n.*572G>A
ENST00000680166.1:n.4277G>A
ENST00000680315.1:n.871G>A
ENST00000680517.1:c.*376G>A ENSP00000505803.1:n.*376G>A
ENST00000680582.1:n.1950G>A
ENST00000680613.1:c.*481G>A ENSP00000506114.1:n.*481G>A
ENST00000680662.1:c.*902G>A ENSP00000505080.1:n.*902G>A
ENST00000680691.1:c.*651G>A ENSP00000506487.1:n.*651G>A
ENST00000680694.1:c.*576G>A ENSP00000505658.1:n.*576G>A
ENST00000680743.1:c.*777G>A ENSP00000505073.1:n.*777G>A
ENST00000680749.1:c.*273G>A ENSP00000505122.1:n.*273G>A
ENST00000680798.1:c.*463G>A ENSP00000505670.1:n.*463G>A
ENST00000680805.1:c.847G>A ENSP00000505447.1:p.Val283Ile
ENST00000680844.1:c.*772G>A ENSP00000506541.1:n.*772G>A
ENST00000680948.1:c.*855G>A ENSP00000505441.1:n.*855G>A
ENST00000680964.1:c.*81G>A ENSP00000505961.1:n.*81G>A
ENST00000681037.1:c.*2472G>A ENSP00000506025.1:n.*2472G>A
ENST00000681063.1:c.*257G>A ENSP00000506616.1:n.*257G>A
ENST00000681209.1:c.*643G>A ENSP00000505877.1:n.*643G>A
ENST00000681278.1:n.1690G>A
ENST00000681289.1:n.4983G>A
ENST00000681361.1:c.*655G>A ENSP00000506679.1:n.*655G>A
ENST00000681430.1:c.*81G>A ENSP00000506301.1:n.*81G>A
ENST00000681446.1:c.*692G>A ENSP00000506244.1:n.*692G>A
ENST00000681450.1:c.*659G>A ENSP00000505660.1:n.*659G>A
ENST00000681548.1:c.*574G>A ENSP00000505275.1:n.*574G>A
ENST00000681616.1:c.*647G>A ENSP00000505111.1:n.*647G>A
ENST00000681621.1:c.*572G>A ENSP00000505770.1:n.*572G>A
ENST00000681680.1:n.3083G>A
ENST00000681720.1:c.*443G>A ENSP00000505438.1:n.*443G>A
ENST00000681730.1:n.1210G>A
ENST00000681790.1:c.730G>A ENSP00000505130.1:p.Val244Ile
ENST00000681837.1:n.1604G>A
ENST00000681913.1:n.3234G>A
ENST00000681916.1:c.*756G>A ENSP00000506477.1:n.*756G>A
ENST00000681930.1:n.3112G>A
ENST00000370834.9:c.1087G>A ENSP00000359871.5:p.Val363Ile
ENST00000370841.8:c.988G>A ENSP00000359878.4:p.Val330Ile
ENST00000420607.6:c.1000G>A ENSP00000409612.2:p.Val334Ile
ENST00000481374.1:n.261G>A
ENST00000525808.5:c.*574G>A ENSP00000434823.1:n.*574G>A
ENST00000526129.5:c.*772G>A ENSP00000434092.1:n.*772G>A
ENST00000526196.5:c.*756G>A ENSP00000431953.1:n.*756G>A
ENST00000528016.1:c.160-8013G>A ENSP00000434284.1:n.160-8013G>A
ENST00000529059.5:n.897G>A
ENST00000532207.5:n.718G>A
ENST00000534334.5:c.*729G>A ENSP00000435584.1:n.*729G>A
ENST00000541113.5:c.880G>A ENSP00000442324.1:p.Val294Ile
NM_000016.5:c.988G>A NP_000007.1:p.Val330Ile
NM_001127328.2:c.1000G>A NP_001120800.1:p.Val334Ile
NM_001286042.1:c.880G>A NP_001272971.1:p.Val294Ile
NM_001286043.1:c.1087G>A NP_001272972.1:p.Val363Ile
NM_001286044.1:c.421G>A NP_001272973.1:p.Val141Ile
NM_000016.6:c.988G>A MANE Select NP_000007.1:p.Val330Ile
NM_001127328.3:c.1000G>A NP_001120800.1:p.Val334Ile
NM_001286042.2:c.880G>A NP_001272971.1:p.Val294Ile
NM_001286043.2:c.1087G>A NP_001272972.1:p.Val363Ile
NM_001286044.2:c.421G>A NP_001272973.1:p.Val141Ile