Canonical Allele Identifier: CA340818035
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761212T>G , CM000663.2:g.75761212T>G GRCh38
NC_000001.10:g.76226897T>G , CM000663.1:g.76226897T>G GRCh37
NC_000001.9:g.75999485T>G NCBI36
NG_007045.2:g.41855T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1036T>G MANE Select ENSP00000359878.5:p.Ser346Ala
ENST00000473018.3:n.3160T>G
ENST00000532207.6:n.2047T>G
ENST00000541113.6:c.940T>G ENSP00000442324.2:p.Ser314Ala
ENST00000679509.1:n.1998T>G
ENST00000679530.1:c.*804T>G ENSP00000506454.1:n.*804T>G
ENST00000679615.1:n.3051T>G
ENST00000679687.1:c.598T>G ENSP00000506598.1:p.Ser200Ala
ENST00000679704.1:c.*802T>G ENSP00000505117.1:n.*802T>G
ENST00000679709.1:c.*999T>G ENSP00000506623.1:n.*999T>G
ENST00000679976.1:c.*620T>G ENSP00000505565.1:n.*620T>G
ENST00000680166.1:n.4325T>G
ENST00000680315.1:n.919T>G
ENST00000680517.1:c.*424T>G ENSP00000505803.1:n.*424T>G
ENST00000680582.1:n.1998T>G
ENST00000680613.1:c.*529T>G ENSP00000506114.1:n.*529T>G
ENST00000680662.1:c.*950T>G ENSP00000505080.1:n.*950T>G
ENST00000680691.1:c.*699T>G ENSP00000506487.1:n.*699T>G
ENST00000680694.1:c.*624T>G ENSP00000505658.1:n.*624T>G
ENST00000680743.1:c.*825T>G ENSP00000505073.1:n.*825T>G
ENST00000680749.1:c.*321T>G ENSP00000505122.1:n.*321T>G
ENST00000680798.1:c.*511T>G ENSP00000505670.1:n.*511T>G
ENST00000680805.1:c.895T>G ENSP00000505447.1:p.Ser299Ala
ENST00000680844.1:c.*820T>G ENSP00000506541.1:n.*820T>G
ENST00000680948.1:c.*903T>G ENSP00000505441.1:n.*903T>G
ENST00000680964.1:c.*129T>G ENSP00000505961.1:n.*129T>G
ENST00000681037.1:c.*2520T>G ENSP00000506025.1:n.*2520T>G
ENST00000681063.1:c.*305T>G ENSP00000506616.1:n.*305T>G
ENST00000681209.1:c.*691T>G ENSP00000505877.1:n.*691T>G
ENST00000681278.1:n.1738T>G
ENST00000681289.1:n.5031T>G
ENST00000681361.1:c.*703T>G ENSP00000506679.1:n.*703T>G
ENST00000681430.1:c.*129T>G ENSP00000506301.1:n.*129T>G
ENST00000681446.1:c.*740T>G ENSP00000506244.1:n.*740T>G
ENST00000681450.1:c.*707T>G ENSP00000505660.1:n.*707T>G
ENST00000681548.1:c.*622T>G ENSP00000505275.1:n.*622T>G
ENST00000681616.1:c.*695T>G ENSP00000505111.1:n.*695T>G
ENST00000681621.1:c.*620T>G ENSP00000505770.1:n.*620T>G
ENST00000681680.1:n.3131T>G
ENST00000681720.1:c.*491T>G ENSP00000505438.1:n.*491T>G
ENST00000681730.1:n.1258T>G
ENST00000681790.1:c.778T>G ENSP00000505130.1:p.Ser260Ala
ENST00000681837.1:n.1652T>G
ENST00000681913.1:n.3282T>G
ENST00000681916.1:c.*804T>G ENSP00000506477.1:n.*804T>G
ENST00000681930.1:n.3160T>G
ENST00000370834.9:c.1135T>G ENSP00000359871.5:p.Ser379Ala
ENST00000370841.8:c.1036T>G ENSP00000359878.4:p.Ser346Ala
ENST00000420607.6:c.1048T>G ENSP00000409612.2:p.Ser350Ala
ENST00000481374.1:n.309T>G
ENST00000525808.5:c.*622T>G ENSP00000434823.1:n.*622T>G
ENST00000526129.5:c.*820T>G ENSP00000434092.1:n.*820T>G
ENST00000526196.5:c.*804T>G ENSP00000431953.1:n.*804T>G
ENST00000528016.1:c.160-7965T>G ENSP00000434284.1:n.160-7965T>G
ENST00000529059.5:n.945T>G
ENST00000534334.5:c.*777T>G ENSP00000435584.1:n.*777T>G
ENST00000541113.5:c.928T>G ENSP00000442324.1:p.Ser310Ala
NM_000016.5:c.1036T>G NP_000007.1:p.Ser346Ala
NM_001127328.2:c.1048T>G NP_001120800.1:p.Ser350Ala
NM_001286042.1:c.928T>G NP_001272971.1:p.Ser310Ala
NM_001286043.1:c.1135T>G NP_001272972.1:p.Ser379Ala
NM_001286044.1:c.469T>G NP_001272973.1:p.Ser157Ala
NM_000016.6:c.1036T>G MANE Select NP_000007.1:p.Ser346Ala
NM_001127328.3:c.1048T>G NP_001120800.1:p.Ser350Ala
NM_001286042.2:c.928T>G NP_001272971.1:p.Ser310Ala
NM_001286043.2:c.1135T>G NP_001272972.1:p.Ser379Ala
NM_001286044.2:c.469T>G NP_001272973.1:p.Ser157Ala