Canonical Allele Identifier: CA340815793
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745810T>G , CM000663.2:g.75745810T>G GRCh38
NC_000001.10:g.76211495T>G , CM000663.1:g.76211495T>G GRCh37
NC_000001.9:g.75984083T>G NCBI36
NG_007045.2:g.26453T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.604T>G MANE Select ENSP00000359878.5:p.Phe202Val
ENST00000473018.3:n.2728T>G
ENST00000532207.6:n.1493T>G
ENST00000541113.6:c.604T>G ENSP00000442324.2:p.Phe202Val
ENST00000679509.1:n.1566T>G
ENST00000679530.1:c.*372T>G ENSP00000506454.1:n.*372T>G
ENST00000679615.1:n.2724-3609T>G
ENST00000679687.1:c.166T>G ENSP00000506598.1:p.Phe56Val
ENST00000679704.1:c.*370T>G ENSP00000505117.1:n.*370T>G
ENST00000679709.1:c.*567T>G ENSP00000506623.1:n.*567T>G
ENST00000679976.1:c.*188T>G ENSP00000505565.1:n.*188T>G
ENST00000680166.1:n.3893T>G
ENST00000680517.1:c.*97-3609T>G ENSP00000505803.1:n.*97-3609T>G
ENST00000680582.1:n.1566T>G
ENST00000680613.1:c.600-25T>G ENSP00000506114.1:n.600-25T>G
ENST00000680662.1:c.*518T>G ENSP00000505080.1:n.*518T>G
ENST00000680691.1:c.*267T>G ENSP00000506487.1:n.*267T>G
ENST00000680694.1:c.*192T>G ENSP00000505658.1:n.*192T>G
ENST00000680743.1:c.*271T>G ENSP00000505073.1:n.*271T>G
ENST00000680749.1:c.600-3609T>G ENSP00000505122.1:n.600-3609T>G
ENST00000680798.1:c.*184-3609T>G ENSP00000505670.1:n.*184-3609T>G
ENST00000680805.1:c.604T>G ENSP00000505447.1:p.Phe202Val
ENST00000680844.1:c.*388T>G ENSP00000506541.1:n.*388T>G
ENST00000680948.1:c.*471T>G ENSP00000505441.1:n.*471T>G
ENST00000680964.1:c.604T>G ENSP00000505961.1:p.Phe202Val
ENST00000681037.1:c.*2113-25T>G ENSP00000506025.1:n.*2113-25T>G
ENST00000681063.1:c.600-4641T>G ENSP00000506616.1:n.600-4641T>G
ENST00000681209.1:c.*364-3609T>G ENSP00000505877.1:n.*364-3609T>G
ENST00000681278.1:n.961T>G
ENST00000681289.1:n.4599T>G
ENST00000681361.1:c.*271T>G ENSP00000506679.1:n.*271T>G
ENST00000681430.1:c.604T>G ENSP00000506301.1:p.Phe202Val
ENST00000681446.1:c.*186T>G ENSP00000506244.1:n.*186T>G
ENST00000681450.1:c.*275T>G ENSP00000505660.1:n.*275T>G
ENST00000681548.1:c.*190T>G ENSP00000505275.1:n.*190T>G
ENST00000681616.1:c.*368-3609T>G ENSP00000505111.1:n.*368-3609T>G
ENST00000681621.1:c.*188T>G ENSP00000505770.1:n.*188T>G
ENST00000681680.1:n.2724-25T>G
ENST00000681720.1:c.*59T>G ENSP00000505438.1:n.*59T>G
ENST00000681730.1:n.826T>G
ENST00000681790.1:c.346T>G ENSP00000505130.1:p.Phe116Val
ENST00000681837.1:n.1220T>G
ENST00000681913.1:n.2728T>G
ENST00000681916.1:c.*372T>G ENSP00000506477.1:n.*372T>G
ENST00000681930.1:n.2728T>G
ENST00000370834.9:c.703T>G ENSP00000359871.5:p.Phe235Val
ENST00000370841.8:c.604T>G ENSP00000359878.4:p.Phe202Val
ENST00000420607.6:c.616T>G ENSP00000409612.2:p.Phe206Val
ENST00000525808.5:c.*190T>G ENSP00000434823.1:n.*190T>G
ENST00000526129.5:c.*388T>G ENSP00000434092.1:n.*388T>G
ENST00000526196.5:c.*372T>G ENSP00000431953.1:n.*372T>G
ENST00000526930.1:n.377T>G
ENST00000529059.5:n.513T>G
ENST00000530953.6:c.*101T>G ENSP00000431372.1:n.*101T>G
ENST00000532207.5:n.334T>G
ENST00000532509.5:c.*368T>G ENSP00000432522.1:n.*368T>G
ENST00000534334.5:c.*188T>G ENSP00000435584.1:n.*188T>G
ENST00000541113.5:c.496T>G ENSP00000442324.1:p.Phe166Val
NM_000016.5:c.604T>G NP_000007.1:p.Phe202Val
NM_001127328.2:c.616T>G NP_001120800.1:p.Phe206Val
NM_001286042.1:c.496T>G NP_001272971.1:p.Phe166Val
NM_001286043.1:c.703T>G NP_001272972.1:p.Phe235Val
NM_001286044.1:c.37T>G NP_001272973.1:p.Phe13Val
NM_000016.6:c.604T>G MANE Select NP_000007.1:p.Phe202Val
NM_001127328.3:c.616T>G NP_001120800.1:p.Phe206Val
NM_001286042.2:c.496T>G NP_001272971.1:p.Phe166Val
NM_001286043.2:c.703T>G NP_001272972.1:p.Phe235Val
NM_001286044.2:c.37T>G NP_001272973.1:p.Phe13Val