Canonical Allele Identifier: CA1176720030
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745832C= , CM000663.2:g.75745832C= GRCh38
NC_000001.10:g.76211517C= , CM000663.1:g.76211517C= GRCh37
NC_000001.9:g.75984105C= NCBI36
NG_007045.2:g.26475C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.626C= MANE Select ENSP00000359878.5:p.Pro209=
ENST00000473018.3:n.2750C=
ENST00000532207.6:n.1515C=
ENST00000541113.6:c.626C= ENSP00000442324.2:p.Pro209=
ENST00000679509.1:n.1588C=
ENST00000679530.1:c.*394C= ENSP00000506454.1:n.*394C=
ENST00000679615.1:n.2724-3587C=
ENST00000679687.1:c.188C= ENSP00000506598.1:p.Pro63=
ENST00000679704.1:c.*392C= ENSP00000505117.1:n.*392C=
ENST00000679709.1:c.*589C= ENSP00000506623.1:n.*589C=
ENST00000679976.1:c.*210C= ENSP00000505565.1:n.*210C=
ENST00000680166.1:n.3915C=
ENST00000680517.1:c.*97-3587C= ENSP00000505803.1:n.*97-3587C=
ENST00000680582.1:n.1588C=
ENST00000680613.1:c.600-3C= ENSP00000506114.1:n.600-3C=
ENST00000680662.1:c.*540C= ENSP00000505080.1:n.*540C=
ENST00000680691.1:c.*289C= ENSP00000506487.1:n.*289C=
ENST00000680694.1:c.*214C= ENSP00000505658.1:n.*214C=
ENST00000680743.1:c.*293C= ENSP00000505073.1:n.*293C=
ENST00000680749.1:c.600-3587C= ENSP00000505122.1:n.600-3587C=
ENST00000680798.1:c.*184-3587C= ENSP00000505670.1:n.*184-3587C=
ENST00000680805.1:c.626C= ENSP00000505447.1:p.Pro209=
ENST00000680844.1:c.*410C= ENSP00000506541.1:n.*410C=
ENST00000680948.1:c.*493C= ENSP00000505441.1:n.*493C=
ENST00000680964.1:c.626C= ENSP00000505961.1:p.Pro209=
ENST00000681037.1:c.*2113-3C= ENSP00000506025.1:n.*2113-3C=
ENST00000681063.1:c.600-4619C= ENSP00000506616.1:n.600-4619C=
ENST00000681209.1:c.*364-3587C= ENSP00000505877.1:n.*364-3587C=
ENST00000681278.1:n.983C=
ENST00000681289.1:n.4621C=
ENST00000681361.1:c.*293C= ENSP00000506679.1:n.*293C=
ENST00000681430.1:c.626C= ENSP00000506301.1:p.Pro209=
ENST00000681446.1:c.*208C= ENSP00000506244.1:n.*208C=
ENST00000681450.1:c.*297C= ENSP00000505660.1:n.*297C=
ENST00000681548.1:c.*212C= ENSP00000505275.1:n.*212C=
ENST00000681616.1:c.*368-3587C= ENSP00000505111.1:n.*368-3587C=
ENST00000681621.1:c.*210C= ENSP00000505770.1:n.*210C=
ENST00000681680.1:n.2724-3C=
ENST00000681720.1:c.*81C= ENSP00000505438.1:n.*81C=
ENST00000681730.1:n.848C=
ENST00000681790.1:c.368C= ENSP00000505130.1:p.Pro123=
ENST00000681837.1:n.1242C=
ENST00000681913.1:n.2750C=
ENST00000681916.1:c.*394C= ENSP00000506477.1:n.*394C=
ENST00000681930.1:n.2750C=
ENST00000370834.9:c.725C= ENSP00000359871.5:p.Pro242=
ENST00000370841.8:c.626C= ENSP00000359878.4:p.Pro209=
ENST00000420607.6:c.638C= ENSP00000409612.2:p.Pro213=
ENST00000525808.5:c.*212C= ENSP00000434823.1:n.*212C=
ENST00000526129.5:c.*410C= ENSP00000434092.1:n.*410C=
ENST00000526196.5:c.*394C= ENSP00000431953.1:n.*394C=
ENST00000526930.1:n.399C=
ENST00000529059.5:n.535C=
ENST00000530953.6:c.*123C= ENSP00000431372.1:n.*123C=
ENST00000532207.5:n.356C=
ENST00000532509.5:c.*390C= ENSP00000432522.1:n.*390C=
ENST00000534334.5:c.*210C= ENSP00000435584.1:n.*210C=
ENST00000541113.5:c.518C= ENSP00000442324.1:p.Pro173=
NM_000016.5:c.626C= NP_000007.1:p.Pro209=
NM_001127328.2:c.638C= NP_001120800.1:p.Pro213=
NM_001286042.1:c.518C= NP_001272971.1:p.Pro173=
NM_001286043.1:c.725C= NP_001272972.1:p.Pro242=
NM_001286044.1:c.59C= NP_001272973.1:p.Pro20=
NM_000016.6:c.626C= MANE Select NP_000007.1:p.Pro209=
NM_001127328.3:c.638C= NP_001120800.1:p.Pro213=
NM_001286042.2:c.518C= NP_001272971.1:p.Pro173=
NM_001286043.2:c.725C= NP_001272972.1:p.Pro242=
NM_001286044.2:c.59C= NP_001272973.1:p.Pro20=