Canonical Allele Identifier: CA340817906
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761154G>C , CM000663.2:g.75761154G>C GRCh38
NC_000001.10:g.76226839G>C , CM000663.1:g.76226839G>C GRCh37
NC_000001.9:g.75999427G>C NCBI36
NG_007045.2:g.41797G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.978G>C MANE Select ENSP00000359878.5:p.Met326Ile
ENST00000473018.3:n.3102G>C
ENST00000532207.6:n.1989G>C
ENST00000541113.6:c.882G>C ENSP00000442324.2:p.Met294Ile
ENST00000679509.1:n.1940G>C
ENST00000679530.1:c.*746G>C ENSP00000506454.1:n.*746G>C
ENST00000679615.1:n.2993G>C
ENST00000679687.1:c.540G>C ENSP00000506598.1:p.Met180Ile
ENST00000679704.1:c.*744G>C ENSP00000505117.1:n.*744G>C
ENST00000679709.1:c.*941G>C ENSP00000506623.1:n.*941G>C
ENST00000679976.1:c.*562G>C ENSP00000505565.1:n.*562G>C
ENST00000680166.1:n.4267G>C
ENST00000680315.1:n.861G>C
ENST00000680517.1:c.*366G>C ENSP00000505803.1:n.*366G>C
ENST00000680582.1:n.1940G>C
ENST00000680613.1:c.*471G>C ENSP00000506114.1:n.*471G>C
ENST00000680662.1:c.*892G>C ENSP00000505080.1:n.*892G>C
ENST00000680691.1:c.*641G>C ENSP00000506487.1:n.*641G>C
ENST00000680694.1:c.*566G>C ENSP00000505658.1:n.*566G>C
ENST00000680743.1:c.*767G>C ENSP00000505073.1:n.*767G>C
ENST00000680749.1:c.*263G>C ENSP00000505122.1:n.*263G>C
ENST00000680798.1:c.*453G>C ENSP00000505670.1:n.*453G>C
ENST00000680805.1:c.837G>C ENSP00000505447.1:p.Met279Ile
ENST00000680844.1:c.*762G>C ENSP00000506541.1:n.*762G>C
ENST00000680948.1:c.*845G>C ENSP00000505441.1:n.*845G>C
ENST00000680964.1:c.*71G>C ENSP00000505961.1:n.*71G>C
ENST00000681037.1:c.*2462G>C ENSP00000506025.1:n.*2462G>C
ENST00000681063.1:c.*247G>C ENSP00000506616.1:n.*247G>C
ENST00000681209.1:c.*633G>C ENSP00000505877.1:n.*633G>C
ENST00000681278.1:n.1680G>C
ENST00000681289.1:n.4973G>C
ENST00000681361.1:c.*645G>C ENSP00000506679.1:n.*645G>C
ENST00000681430.1:c.*71G>C ENSP00000506301.1:n.*71G>C
ENST00000681446.1:c.*682G>C ENSP00000506244.1:n.*682G>C
ENST00000681450.1:c.*649G>C ENSP00000505660.1:n.*649G>C
ENST00000681548.1:c.*564G>C ENSP00000505275.1:n.*564G>C
ENST00000681616.1:c.*637G>C ENSP00000505111.1:n.*637G>C
ENST00000681621.1:c.*562G>C ENSP00000505770.1:n.*562G>C
ENST00000681680.1:n.3073G>C
ENST00000681720.1:c.*433G>C ENSP00000505438.1:n.*433G>C
ENST00000681730.1:n.1200G>C
ENST00000681790.1:c.720G>C ENSP00000505130.1:p.Met240Ile
ENST00000681837.1:n.1594G>C
ENST00000681913.1:n.3224G>C
ENST00000681916.1:c.*746G>C ENSP00000506477.1:n.*746G>C
ENST00000681930.1:n.3102G>C
ENST00000370834.9:c.1077G>C ENSP00000359871.5:p.Met359Ile
ENST00000370841.8:c.978G>C ENSP00000359878.4:p.Met326Ile
ENST00000420607.6:c.990G>C ENSP00000409612.2:p.Met330Ile
ENST00000481374.1:n.251G>C
ENST00000525808.5:c.*564G>C ENSP00000434823.1:n.*564G>C
ENST00000526129.5:c.*762G>C ENSP00000434092.1:n.*762G>C
ENST00000526196.5:c.*746G>C ENSP00000431953.1:n.*746G>C
ENST00000528016.1:c.160-8023G>C ENSP00000434284.1:n.160-8023G>C
ENST00000529059.5:n.887G>C
ENST00000532207.5:n.708G>C
ENST00000534334.5:c.*719G>C ENSP00000435584.1:n.*719G>C
ENST00000541113.5:c.870G>C ENSP00000442324.1:p.Met290Ile
NM_000016.5:c.978G>C NP_000007.1:p.Met326Ile
NM_001127328.2:c.990G>C NP_001120800.1:p.Met330Ile
NM_001286042.1:c.870G>C NP_001272971.1:p.Met290Ile
NM_001286043.1:c.1077G>C NP_001272972.1:p.Met359Ile
NM_001286044.1:c.411G>C NP_001272973.1:p.Met137Ile
NM_000016.6:c.978G>C MANE Select NP_000007.1:p.Met326Ile
NM_001127328.3:c.990G>C NP_001120800.1:p.Met330Ile
NM_001286042.2:c.870G>C NP_001272971.1:p.Met290Ile
NM_001286043.2:c.1077G>C NP_001272972.1:p.Met359Ile
NM_001286044.2:c.411G>C NP_001272973.1:p.Met137Ile