Canonical Allele Identifier: CA1176721437
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749433C= , CM000663.2:g.75749433C= GRCh38
NC_000001.10:g.76215118C= , CM000663.1:g.76215118C= GRCh37
NC_000001.9:g.75987706C= NCBI36
NG_007045.2:g.30076C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.723C= MANE Select ENSP00000359878.5:p.Gly241=
ENST00000473018.3:n.2847C=
ENST00000532207.6:n.1612C=
ENST00000541113.6:c.723C= ENSP00000442324.2:p.Gly241=
ENST00000679509.1:n.1685C=
ENST00000679530.1:c.*491C= ENSP00000506454.1:n.*491C=
ENST00000679615.1:n.2738C=
ENST00000679687.1:c.285C= ENSP00000506598.1:p.Gly95=
ENST00000679704.1:c.*489C= ENSP00000505117.1:n.*489C=
ENST00000679709.1:c.*686C= ENSP00000506623.1:n.*686C=
ENST00000679976.1:c.*307C= ENSP00000505565.1:n.*307C=
ENST00000680166.1:n.4012C=
ENST00000680517.1:c.*111C= ENSP00000505803.1:n.*111C=
ENST00000680582.1:n.1685C=
ENST00000680613.1:c.*94C= ENSP00000506114.1:n.*94C=
ENST00000680662.1:c.*637C= ENSP00000505080.1:n.*637C=
ENST00000680691.1:c.*386C= ENSP00000506487.1:n.*386C=
ENST00000680694.1:c.*311C= ENSP00000505658.1:n.*311C=
ENST00000680743.1:c.*390C= ENSP00000505073.1:n.*390C=
ENST00000680749.1:c.*8C= ENSP00000505122.1:n.*8C=
ENST00000680798.1:c.*198C= ENSP00000505670.1:n.*198C=
ENST00000680805.1:c.709-1018C= ENSP00000505447.1:n.709-1018C=
ENST00000680844.1:c.*507C= ENSP00000506541.1:n.*507C=
ENST00000680948.1:c.*590C= ENSP00000505441.1:n.*590C=
ENST00000680964.1:c.723C= ENSP00000505961.1:p.Gly241=
ENST00000681037.1:c.*2207C= ENSP00000506025.1:n.*2207C=
ENST00000681063.1:c.600-1018C= ENSP00000506616.1:n.600-1018C=
ENST00000681209.1:c.*378C= ENSP00000505877.1:n.*378C=
ENST00000681278.1:n.1080C=
ENST00000681289.1:n.4718C=
ENST00000681361.1:c.*390C= ENSP00000506679.1:n.*390C=
ENST00000681430.1:c.723C= ENSP00000506301.1:p.Gly241=
ENST00000681446.1:c.*305C= ENSP00000506244.1:n.*305C=
ENST00000681450.1:c.*394C= ENSP00000505660.1:n.*394C=
ENST00000681548.1:c.*309C= ENSP00000505275.1:n.*309C=
ENST00000681616.1:c.*382C= ENSP00000505111.1:n.*382C=
ENST00000681621.1:c.*307C= ENSP00000505770.1:n.*307C=
ENST00000681680.1:n.2818C=
ENST00000681720.1:c.*178C= ENSP00000505438.1:n.*178C=
ENST00000681730.1:n.945C=
ENST00000681790.1:c.465C= ENSP00000505130.1:p.Gly155=
ENST00000681837.1:n.1339C=
ENST00000681913.1:n.2847C=
ENST00000681916.1:c.*491C= ENSP00000506477.1:n.*491C=
ENST00000681930.1:n.2847C=
ENST00000370834.9:c.822C= ENSP00000359871.5:p.Gly274=
ENST00000370841.8:c.723C= ENSP00000359878.4:p.Gly241=
ENST00000420607.6:c.735C= ENSP00000409612.2:p.Gly245=
ENST00000525808.5:c.*309C= ENSP00000434823.1:n.*309C=
ENST00000526129.5:c.*507C= ENSP00000434092.1:n.*507C=
ENST00000526196.5:c.*491C= ENSP00000431953.1:n.*491C=
ENST00000526930.1:n.496C=
ENST00000529059.5:n.632C=
ENST00000530953.6:c.*220C= ENSP00000431372.1:n.*220C=
ENST00000532207.5:n.453C=
ENST00000532509.5:c.*487C= ENSP00000432522.1:n.*487C=
ENST00000534334.5:c.*307C= ENSP00000435584.1:n.*307C=
ENST00000541113.5:c.615C= ENSP00000442324.1:p.Gly205=
NM_000016.5:c.723C= NP_000007.1:p.Gly241=
NM_001127328.2:c.735C= NP_001120800.1:p.Gly245=
NM_001286042.1:c.615C= NP_001272971.1:p.Gly205=
NM_001286043.1:c.822C= NP_001272972.1:p.Gly274=
NM_001286044.1:c.156C= NP_001272973.1:p.Gly52=
NM_000016.6:c.723C= MANE Select NP_000007.1:p.Gly241=
NM_001127328.3:c.735C= NP_001120800.1:p.Gly245=
NM_001286042.2:c.615C= NP_001272971.1:p.Gly205=
NM_001286043.2:c.822C= NP_001272972.1:p.Gly274=
NM_001286044.2:c.156C= NP_001272973.1:p.Gly52=