Canonical Allele Identifier: CA340818321
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761349G>C , CM000663.2:g.75761349G>C GRCh38
NC_000001.10:g.76227034G>C , CM000663.1:g.76227034G>C GRCh37
NC_000001.9:g.75999622G>C NCBI36
NG_007045.2:g.41992G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1173G>C MANE Select ENSP00000359878.5:p.Met391Ile
ENST00000473018.3:n.3297G>C
ENST00000532207.6:n.2184G>C
ENST00000541113.6:c.1077G>C ENSP00000442324.2:p.Met359Ile
ENST00000679509.1:n.2135G>C
ENST00000679530.1:c.*941G>C ENSP00000506454.1:n.*941G>C
ENST00000679615.1:n.3188G>C
ENST00000679687.1:c.735G>C ENSP00000506598.1:p.Met245Ile
ENST00000679704.1:c.*939G>C ENSP00000505117.1:n.*939G>C
ENST00000679709.1:c.*1136G>C ENSP00000506623.1:n.*1136G>C
ENST00000679976.1:c.*757G>C ENSP00000505565.1:n.*757G>C
ENST00000680166.1:n.4462G>C
ENST00000680315.1:n.1056G>C
ENST00000680517.1:c.*561G>C ENSP00000505803.1:n.*561G>C
ENST00000680582.1:n.2135G>C
ENST00000680613.1:c.*666G>C ENSP00000506114.1:n.*666G>C
ENST00000680662.1:c.*1087G>C ENSP00000505080.1:n.*1087G>C
ENST00000680691.1:c.*836G>C ENSP00000506487.1:n.*836G>C
ENST00000680694.1:c.*761G>C ENSP00000505658.1:n.*761G>C
ENST00000680743.1:c.*962G>C ENSP00000505073.1:n.*962G>C
ENST00000680749.1:c.*458G>C ENSP00000505122.1:n.*458G>C
ENST00000680798.1:c.*648G>C ENSP00000505670.1:n.*648G>C
ENST00000680805.1:c.1032G>C ENSP00000505447.1:p.Met344Ile
ENST00000680844.1:c.*957G>C ENSP00000506541.1:n.*957G>C
ENST00000680948.1:c.*1040G>C ENSP00000505441.1:n.*1040G>C
ENST00000680964.1:c.*266G>C ENSP00000505961.1:n.*266G>C
ENST00000681037.1:c.*2657G>C ENSP00000506025.1:n.*2657G>C
ENST00000681063.1:c.*442G>C ENSP00000506616.1:n.*442G>C
ENST00000681209.1:c.*828G>C ENSP00000505877.1:n.*828G>C
ENST00000681278.1:n.1875G>C
ENST00000681289.1:n.5168G>C
ENST00000681361.1:c.*840G>C ENSP00000506679.1:n.*840G>C
ENST00000681430.1:c.*266G>C ENSP00000506301.1:n.*266G>C
ENST00000681446.1:c.*877G>C ENSP00000506244.1:n.*877G>C
ENST00000681450.1:c.*844G>C ENSP00000505660.1:n.*844G>C
ENST00000681548.1:c.*759G>C ENSP00000505275.1:n.*759G>C
ENST00000681616.1:c.*832G>C ENSP00000505111.1:n.*832G>C
ENST00000681621.1:c.*757G>C ENSP00000505770.1:n.*757G>C
ENST00000681680.1:n.3268G>C
ENST00000681720.1:c.*628G>C ENSP00000505438.1:n.*628G>C
ENST00000681730.1:n.1395G>C
ENST00000681790.1:c.915G>C ENSP00000505130.1:p.Met305Ile
ENST00000681837.1:n.1789G>C
ENST00000681913.1:n.3419G>C
ENST00000681916.1:c.*941G>C ENSP00000506477.1:n.*941G>C
ENST00000681930.1:n.3297G>C
ENST00000370834.9:c.1272G>C ENSP00000359871.5:p.Met424Ile
ENST00000370841.8:c.1173G>C ENSP00000359878.4:p.Met391Ile
ENST00000420607.6:c.1185G>C ENSP00000409612.2:p.Met395Ile
ENST00000481374.1:n.446G>C
ENST00000525808.5:c.*759G>C ENSP00000434823.1:n.*759G>C
ENST00000526129.5:c.*957G>C ENSP00000434092.1:n.*957G>C
ENST00000526196.5:c.*941G>C ENSP00000431953.1:n.*941G>C
ENST00000528016.1:c.160-7828G>C ENSP00000434284.1:n.160-7828G>C
ENST00000529059.5:n.1082G>C
ENST00000541113.5:c.1065G>C ENSP00000442324.1:p.Met355Ile
NM_000016.5:c.1173G>C NP_000007.1:p.Met391Ile
NM_001127328.2:c.1185G>C NP_001120800.1:p.Met395Ile
NM_001286042.1:c.1065G>C NP_001272971.1:p.Met355Ile
NM_001286043.1:c.1272G>C NP_001272972.1:p.Met424Ile
NM_001286044.1:c.606G>C NP_001272973.1:p.Met202Ile
NM_000016.6:c.1173G>C MANE Select NP_000007.1:p.Met391Ile
NM_001127328.3:c.1185G>C NP_001120800.1:p.Met395Ile
NM_001286042.2:c.1065G>C NP_001272971.1:p.Met355Ile
NM_001286043.2:c.1272G>C NP_001272972.1:p.Met424Ile
NM_001286044.2:c.606G>C NP_001272973.1:p.Met202Ile