Canonical Allele Identifier: CA340818164
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761275C>A , CM000663.2:g.75761275C>A GRCh38
NC_000001.10:g.76226960C>A , CM000663.1:g.76226960C>A GRCh37
NC_000001.9:g.75999548C>A NCBI36
NG_007045.2:g.41918C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1099C>A MANE Select ENSP00000359878.5:p.Gln367Lys
ENST00000473018.3:n.3223C>A
ENST00000532207.6:n.2110C>A
ENST00000541113.6:c.1003C>A ENSP00000442324.2:p.Gln335Lys
ENST00000679509.1:n.2061C>A
ENST00000679530.1:c.*867C>A ENSP00000506454.1:n.*867C>A
ENST00000679615.1:n.3114C>A
ENST00000679687.1:c.661C>A ENSP00000506598.1:p.Gln221Lys
ENST00000679704.1:c.*865C>A ENSP00000505117.1:n.*865C>A
ENST00000679709.1:c.*1062C>A ENSP00000506623.1:n.*1062C>A
ENST00000679976.1:c.*683C>A ENSP00000505565.1:n.*683C>A
ENST00000680166.1:n.4388C>A
ENST00000680315.1:n.982C>A
ENST00000680517.1:c.*487C>A ENSP00000505803.1:n.*487C>A
ENST00000680582.1:n.2061C>A
ENST00000680613.1:c.*592C>A ENSP00000506114.1:n.*592C>A
ENST00000680662.1:c.*1013C>A ENSP00000505080.1:n.*1013C>A
ENST00000680691.1:c.*762C>A ENSP00000506487.1:n.*762C>A
ENST00000680694.1:c.*687C>A ENSP00000505658.1:n.*687C>A
ENST00000680743.1:c.*888C>A ENSP00000505073.1:n.*888C>A
ENST00000680749.1:c.*384C>A ENSP00000505122.1:n.*384C>A
ENST00000680798.1:c.*574C>A ENSP00000505670.1:n.*574C>A
ENST00000680805.1:c.958C>A ENSP00000505447.1:p.Gln320Lys
ENST00000680844.1:c.*883C>A ENSP00000506541.1:n.*883C>A
ENST00000680948.1:c.*966C>A ENSP00000505441.1:n.*966C>A
ENST00000680964.1:c.*192C>A ENSP00000505961.1:n.*192C>A
ENST00000681037.1:c.*2583C>A ENSP00000506025.1:n.*2583C>A
ENST00000681063.1:c.*368C>A ENSP00000506616.1:n.*368C>A
ENST00000681209.1:c.*754C>A ENSP00000505877.1:n.*754C>A
ENST00000681278.1:n.1801C>A
ENST00000681289.1:n.5094C>A
ENST00000681361.1:c.*766C>A ENSP00000506679.1:n.*766C>A
ENST00000681430.1:c.*192C>A ENSP00000506301.1:n.*192C>A
ENST00000681446.1:c.*803C>A ENSP00000506244.1:n.*803C>A
ENST00000681450.1:c.*770C>A ENSP00000505660.1:n.*770C>A
ENST00000681548.1:c.*685C>A ENSP00000505275.1:n.*685C>A
ENST00000681616.1:c.*758C>A ENSP00000505111.1:n.*758C>A
ENST00000681621.1:c.*683C>A ENSP00000505770.1:n.*683C>A
ENST00000681680.1:n.3194C>A
ENST00000681720.1:c.*554C>A ENSP00000505438.1:n.*554C>A
ENST00000681730.1:n.1321C>A
ENST00000681790.1:c.841C>A ENSP00000505130.1:p.Gln281Lys
ENST00000681837.1:n.1715C>A
ENST00000681913.1:n.3345C>A
ENST00000681916.1:c.*867C>A ENSP00000506477.1:n.*867C>A
ENST00000681930.1:n.3223C>A
ENST00000370834.9:c.1198C>A ENSP00000359871.5:p.Gln400Lys
ENST00000370841.8:c.1099C>A ENSP00000359878.4:p.Gln367Lys
ENST00000420607.6:c.1111C>A ENSP00000409612.2:p.Gln371Lys
ENST00000481374.1:n.372C>A
ENST00000525808.5:c.*685C>A ENSP00000434823.1:n.*685C>A
ENST00000526129.5:c.*883C>A ENSP00000434092.1:n.*883C>A
ENST00000526196.5:c.*867C>A ENSP00000431953.1:n.*867C>A
ENST00000528016.1:c.160-7902C>A ENSP00000434284.1:n.160-7902C>A
ENST00000529059.5:n.1008C>A
ENST00000541113.5:c.991C>A ENSP00000442324.1:p.Gln331Lys
NM_000016.5:c.1099C>A NP_000007.1:p.Gln367Lys
NM_001127328.2:c.1111C>A NP_001120800.1:p.Gln371Lys
NM_001286042.1:c.991C>A NP_001272971.1:p.Gln331Lys
NM_001286043.1:c.1198C>A NP_001272972.1:p.Gln400Lys
NM_001286044.1:c.532C>A NP_001272973.1:p.Gln178Lys
NM_000016.6:c.1099C>A MANE Select NP_000007.1:p.Gln367Lys
NM_001127328.3:c.1111C>A NP_001120800.1:p.Gln371Lys
NM_001286042.2:c.991C>A NP_001272971.1:p.Gln331Lys
NM_001286043.2:c.1198C>A NP_001272972.1:p.Gln400Lys
NM_001286044.2:c.532C>A NP_001272973.1:p.Gln178Lys