Canonical Allele Identifier: CA340818007
Gene: ACADM HGNC NCBI

Linked Data

gnomAD v4: 1-75761200-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761200T>C , CM000663.2:g.75761200T>C GRCh38
NC_000001.10:g.76226885T>C , CM000663.1:g.76226885T>C GRCh37
NC_000001.9:g.75999473T>C NCBI36
NG_007045.2:g.41843T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1024T>C MANE Select ENSP00000359878.5:p.Trp342Arg
ENST00000473018.3:n.3148T>C
ENST00000532207.6:n.2035T>C
ENST00000541113.6:c.928T>C ENSP00000442324.2:p.Trp310Arg
ENST00000679509.1:n.1986T>C
ENST00000679530.1:c.*792T>C ENSP00000506454.1:n.*792T>C
ENST00000679615.1:n.3039T>C
ENST00000679687.1:c.586T>C ENSP00000506598.1:p.Trp196Arg
ENST00000679704.1:c.*790T>C ENSP00000505117.1:n.*790T>C
ENST00000679709.1:c.*987T>C ENSP00000506623.1:n.*987T>C
ENST00000679976.1:c.*608T>C ENSP00000505565.1:n.*608T>C
ENST00000680166.1:n.4313T>C
ENST00000680315.1:n.907T>C
ENST00000680517.1:c.*412T>C ENSP00000505803.1:n.*412T>C
ENST00000680582.1:n.1986T>C
ENST00000680613.1:c.*517T>C ENSP00000506114.1:n.*517T>C
ENST00000680662.1:c.*938T>C ENSP00000505080.1:n.*938T>C
ENST00000680691.1:c.*687T>C ENSP00000506487.1:n.*687T>C
ENST00000680694.1:c.*612T>C ENSP00000505658.1:n.*612T>C
ENST00000680743.1:c.*813T>C ENSP00000505073.1:n.*813T>C
ENST00000680749.1:c.*309T>C ENSP00000505122.1:n.*309T>C
ENST00000680798.1:c.*499T>C ENSP00000505670.1:n.*499T>C
ENST00000680805.1:c.883T>C ENSP00000505447.1:p.Trp295Arg
ENST00000680844.1:c.*808T>C ENSP00000506541.1:n.*808T>C
ENST00000680948.1:c.*891T>C ENSP00000505441.1:n.*891T>C
ENST00000680964.1:c.*117T>C ENSP00000505961.1:n.*117T>C
ENST00000681037.1:c.*2508T>C ENSP00000506025.1:n.*2508T>C
ENST00000681063.1:c.*293T>C ENSP00000506616.1:n.*293T>C
ENST00000681209.1:c.*679T>C ENSP00000505877.1:n.*679T>C
ENST00000681278.1:n.1726T>C
ENST00000681289.1:n.5019T>C
ENST00000681361.1:c.*691T>C ENSP00000506679.1:n.*691T>C
ENST00000681430.1:c.*117T>C ENSP00000506301.1:n.*117T>C
ENST00000681446.1:c.*728T>C ENSP00000506244.1:n.*728T>C
ENST00000681450.1:c.*695T>C ENSP00000505660.1:n.*695T>C
ENST00000681548.1:c.*610T>C ENSP00000505275.1:n.*610T>C
ENST00000681616.1:c.*683T>C ENSP00000505111.1:n.*683T>C
ENST00000681621.1:c.*608T>C ENSP00000505770.1:n.*608T>C
ENST00000681680.1:n.3119T>C
ENST00000681720.1:c.*479T>C ENSP00000505438.1:n.*479T>C
ENST00000681730.1:n.1246T>C
ENST00000681790.1:c.766T>C ENSP00000505130.1:p.Trp256Arg
ENST00000681837.1:n.1640T>C
ENST00000681913.1:n.3270T>C
ENST00000681916.1:c.*792T>C ENSP00000506477.1:n.*792T>C
ENST00000681930.1:n.3148T>C
ENST00000370834.9:c.1123T>C ENSP00000359871.5:p.Trp375Arg
ENST00000370841.8:c.1024T>C ENSP00000359878.4:p.Trp342Arg
ENST00000420607.6:c.1036T>C ENSP00000409612.2:p.Trp346Arg
ENST00000481374.1:n.297T>C
ENST00000525808.5:c.*610T>C ENSP00000434823.1:n.*610T>C
ENST00000526129.5:c.*808T>C ENSP00000434092.1:n.*808T>C
ENST00000526196.5:c.*792T>C ENSP00000431953.1:n.*792T>C
ENST00000528016.1:c.160-7977T>C ENSP00000434284.1:n.160-7977T>C
ENST00000529059.5:n.933T>C
ENST00000532207.5:n.754T>C
ENST00000534334.5:c.*765T>C ENSP00000435584.1:n.*765T>C
ENST00000541113.5:c.916T>C ENSP00000442324.1:p.Trp306Arg
NM_000016.5:c.1024T>C NP_000007.1:p.Trp342Arg
NM_001127328.2:c.1036T>C NP_001120800.1:p.Trp346Arg
NM_001286042.1:c.916T>C NP_001272971.1:p.Trp306Arg
NM_001286043.1:c.1123T>C NP_001272972.1:p.Trp375Arg
NM_001286044.1:c.457T>C NP_001272973.1:p.Trp153Arg
NM_000016.6:c.1024T>C MANE Select NP_000007.1:p.Trp342Arg
NM_001127328.3:c.1036T>C NP_001120800.1:p.Trp346Arg
NM_001286042.2:c.916T>C NP_001272971.1:p.Trp306Arg
NM_001286043.2:c.1123T>C NP_001272972.1:p.Trp375Arg
NM_001286044.2:c.457T>C NP_001272973.1:p.Trp153Arg