Canonical Allele Identifier: CA340818370
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761370G>C , CM000663.2:g.75761370G>C GRCh38
NC_000001.10:g.76227055G>C , CM000663.1:g.76227055G>C GRCh37
NC_000001.9:g.75999643G>C NCBI36
NG_007045.2:g.42013G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1194G>C MANE Select ENSP00000359878.5:p.Gln398His
ENST00000473018.3:n.3318G>C
ENST00000532207.6:n.2205G>C
ENST00000541113.6:c.1098G>C ENSP00000442324.2:p.Gln366His
ENST00000679509.1:n.2156G>C
ENST00000679530.1:c.*962G>C ENSP00000506454.1:n.*962G>C
ENST00000679615.1:n.3209G>C
ENST00000679687.1:c.756G>C ENSP00000506598.1:p.Gln252His
ENST00000679704.1:c.*960G>C ENSP00000505117.1:n.*960G>C
ENST00000679709.1:c.*1157G>C ENSP00000506623.1:n.*1157G>C
ENST00000679976.1:c.*778G>C ENSP00000505565.1:n.*778G>C
ENST00000680166.1:n.4483G>C
ENST00000680315.1:n.1077G>C
ENST00000680517.1:c.*582G>C ENSP00000505803.1:n.*582G>C
ENST00000680582.1:n.2156G>C
ENST00000680613.1:c.*687G>C ENSP00000506114.1:n.*687G>C
ENST00000680662.1:c.*1108G>C ENSP00000505080.1:n.*1108G>C
ENST00000680691.1:c.*857G>C ENSP00000506487.1:n.*857G>C
ENST00000680694.1:c.*782G>C ENSP00000505658.1:n.*782G>C
ENST00000680743.1:c.*983G>C ENSP00000505073.1:n.*983G>C
ENST00000680749.1:c.*479G>C ENSP00000505122.1:n.*479G>C
ENST00000680798.1:c.*669G>C ENSP00000505670.1:n.*669G>C
ENST00000680805.1:c.1053G>C ENSP00000505447.1:p.Gln351His
ENST00000680844.1:c.*978G>C ENSP00000506541.1:n.*978G>C
ENST00000680948.1:c.*1061G>C ENSP00000505441.1:n.*1061G>C
ENST00000680964.1:c.*287G>C ENSP00000505961.1:n.*287G>C
ENST00000681037.1:c.*2678G>C ENSP00000506025.1:n.*2678G>C
ENST00000681063.1:c.*463G>C ENSP00000506616.1:n.*463G>C
ENST00000681209.1:c.*849G>C ENSP00000505877.1:n.*849G>C
ENST00000681278.1:n.1896G>C
ENST00000681289.1:n.5189G>C
ENST00000681361.1:c.*861G>C ENSP00000506679.1:n.*861G>C
ENST00000681430.1:c.*287G>C ENSP00000506301.1:n.*287G>C
ENST00000681446.1:c.*898G>C ENSP00000506244.1:n.*898G>C
ENST00000681450.1:c.*865G>C ENSP00000505660.1:n.*865G>C
ENST00000681548.1:c.*780G>C ENSP00000505275.1:n.*780G>C
ENST00000681616.1:c.*853G>C ENSP00000505111.1:n.*853G>C
ENST00000681621.1:c.*778G>C ENSP00000505770.1:n.*778G>C
ENST00000681680.1:n.3289G>C
ENST00000681720.1:c.*649G>C ENSP00000505438.1:n.*649G>C
ENST00000681730.1:n.1416G>C
ENST00000681790.1:c.936G>C ENSP00000505130.1:p.Gln312His
ENST00000681837.1:n.1810G>C
ENST00000681913.1:n.3440G>C
ENST00000681916.1:c.*962G>C ENSP00000506477.1:n.*962G>C
ENST00000681930.1:n.3318G>C
ENST00000370834.9:c.1293G>C ENSP00000359871.5:p.Gln431His
ENST00000370841.8:c.1194G>C ENSP00000359878.4:p.Gln398His
ENST00000420607.6:c.1206G>C ENSP00000409612.2:p.Gln402His
ENST00000481374.1:n.467G>C
ENST00000525808.5:c.*780G>C ENSP00000434823.1:n.*780G>C
ENST00000526129.5:c.*978G>C ENSP00000434092.1:n.*978G>C
ENST00000526196.5:c.*962G>C ENSP00000431953.1:n.*962G>C
ENST00000528016.1:c.160-7807G>C ENSP00000434284.1:n.160-7807G>C
ENST00000529059.5:n.1103G>C
ENST00000541113.5:c.1086G>C ENSP00000442324.1:p.Gln362His
NM_000016.5:c.1194G>C NP_000007.1:p.Gln398His
NM_001127328.2:c.1206G>C NP_001120800.1:p.Gln402His
NM_001286042.1:c.1086G>C NP_001272971.1:p.Gln362His
NM_001286043.1:c.1293G>C NP_001272972.1:p.Gln431His
NM_001286044.1:c.627G>C NP_001272973.1:p.Gln209His
NM_000016.6:c.1194G>C MANE Select NP_000007.1:p.Gln398His
NM_001127328.3:c.1206G>C NP_001120800.1:p.Gln402His
NM_001286042.2:c.1086G>C NP_001272971.1:p.Gln362His
NM_001286043.2:c.1293G>C NP_001272972.1:p.Gln431His
NM_001286044.2:c.627G>C NP_001272973.1:p.Gln209His