Canonical Allele Identifier: CA913267
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 458788
ClinVar RCV Id: RCV000543549
dbSNP Id: rs771978135
gnomAD v2: 1-76226895-A-T
gnomAD v4: 1-75761210-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761210A>T , CM000663.2:g.75761210A>T GRCh38
NC_000001.10:g.76226895A>T , CM000663.1:g.76226895A>T GRCh37
NC_000001.9:g.75999483A>T NCBI36
NG_007045.2:g.41853A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1034A>T MANE Select ENSP00000359878.5:p.Asp345Val
ENST00000473018.3:n.3158A>T
ENST00000532207.6:n.2045A>T
ENST00000541113.6:c.938A>T ENSP00000442324.2:p.Asp313Val
ENST00000679509.1:n.1996A>T
ENST00000679530.1:c.*802A>T ENSP00000506454.1:n.*802A>T
ENST00000679615.1:n.3049A>T
ENST00000679687.1:c.596A>T ENSP00000506598.1:p.Asp199Val
ENST00000679704.1:c.*800A>T ENSP00000505117.1:n.*800A>T
ENST00000679709.1:c.*997A>T ENSP00000506623.1:n.*997A>T
ENST00000679976.1:c.*618A>T ENSP00000505565.1:n.*618A>T
ENST00000680166.1:n.4323A>T
ENST00000680315.1:n.917A>T
ENST00000680517.1:c.*422A>T ENSP00000505803.1:n.*422A>T
ENST00000680582.1:n.1996A>T
ENST00000680613.1:c.*527A>T ENSP00000506114.1:n.*527A>T
ENST00000680662.1:c.*948A>T ENSP00000505080.1:n.*948A>T
ENST00000680691.1:c.*697A>T ENSP00000506487.1:n.*697A>T
ENST00000680694.1:c.*622A>T ENSP00000505658.1:n.*622A>T
ENST00000680743.1:c.*823A>T ENSP00000505073.1:n.*823A>T
ENST00000680749.1:c.*319A>T ENSP00000505122.1:n.*319A>T
ENST00000680798.1:c.*509A>T ENSP00000505670.1:n.*509A>T
ENST00000680805.1:c.893A>T ENSP00000505447.1:p.Asp298Val
ENST00000680844.1:c.*818A>T ENSP00000506541.1:n.*818A>T
ENST00000680948.1:c.*901A>T ENSP00000505441.1:n.*901A>T
ENST00000680964.1:c.*127A>T ENSP00000505961.1:n.*127A>T
ENST00000681037.1:c.*2518A>T ENSP00000506025.1:n.*2518A>T
ENST00000681063.1:c.*303A>T ENSP00000506616.1:n.*303A>T
ENST00000681209.1:c.*689A>T ENSP00000505877.1:n.*689A>T
ENST00000681278.1:n.1736A>T
ENST00000681289.1:n.5029A>T
ENST00000681361.1:c.*701A>T ENSP00000506679.1:n.*701A>T
ENST00000681430.1:c.*127A>T ENSP00000506301.1:n.*127A>T
ENST00000681446.1:c.*738A>T ENSP00000506244.1:n.*738A>T
ENST00000681450.1:c.*705A>T ENSP00000505660.1:n.*705A>T
ENST00000681548.1:c.*620A>T ENSP00000505275.1:n.*620A>T
ENST00000681616.1:c.*693A>T ENSP00000505111.1:n.*693A>T
ENST00000681621.1:c.*618A>T ENSP00000505770.1:n.*618A>T
ENST00000681680.1:n.3129A>T
ENST00000681720.1:c.*489A>T ENSP00000505438.1:n.*489A>T
ENST00000681730.1:n.1256A>T
ENST00000681790.1:c.776A>T ENSP00000505130.1:p.Asp259Val
ENST00000681837.1:n.1650A>T
ENST00000681913.1:n.3280A>T
ENST00000681916.1:c.*802A>T ENSP00000506477.1:n.*802A>T
ENST00000681930.1:n.3158A>T
ENST00000370834.9:c.1133A>T ENSP00000359871.5:p.Asp378Val
ENST00000370841.8:c.1034A>T ENSP00000359878.4:p.Asp345Val
ENST00000420607.6:c.1046A>T ENSP00000409612.2:p.Asp349Val
ENST00000481374.1:n.307A>T
ENST00000525808.5:c.*620A>T ENSP00000434823.1:n.*620A>T
ENST00000526129.5:c.*818A>T ENSP00000434092.1:n.*818A>T
ENST00000526196.5:c.*802A>T ENSP00000431953.1:n.*802A>T
ENST00000528016.1:c.160-7967A>T ENSP00000434284.1:n.160-7967A>T
ENST00000529059.5:n.943A>T
ENST00000534334.5:c.*775A>T ENSP00000435584.1:n.*775A>T
ENST00000541113.5:c.926A>T ENSP00000442324.1:p.Asp309Val
NM_000016.5:c.1034A>T NP_000007.1:p.Asp345Val
NM_001127328.2:c.1046A>T NP_001120800.1:p.Asp349Val
NM_001286042.1:c.926A>T NP_001272971.1:p.Asp309Val
NM_001286043.1:c.1133A>T NP_001272972.1:p.Asp378Val
NM_001286044.1:c.467A>T NP_001272973.1:p.Asp156Val
NM_000016.6:c.1034A>T MANE Select NP_000007.1:p.Asp345Val
NM_001127328.3:c.1046A>T NP_001120800.1:p.Asp349Val
NM_001286042.2:c.926A>T NP_001272971.1:p.Asp309Val
NM_001286043.2:c.1133A>T NP_001272972.1:p.Asp378Val
NM_001286044.2:c.467A>T NP_001272973.1:p.Asp156Val