Canonical Allele Identifier: CA1176721445
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749458A= , CM000663.2:g.75749458A= GRCh38
NC_000001.10:g.76215143A= , CM000663.1:g.76215143A= GRCh37
NC_000001.9:g.75987731A= NCBI36
NG_007045.2:g.30101A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.748A= MANE Select ENSP00000359878.5:p.Ile250=
ENST00000473018.3:n.2872A=
ENST00000532207.6:n.1637A=
ENST00000541113.6:c.748A= ENSP00000442324.2:p.Ile250=
ENST00000679509.1:n.1710A=
ENST00000679530.1:c.*516A= ENSP00000506454.1:n.*516A=
ENST00000679615.1:n.2763A=
ENST00000679687.1:c.310A= ENSP00000506598.1:p.Ile104=
ENST00000679704.1:c.*514A= ENSP00000505117.1:n.*514A=
ENST00000679709.1:c.*711A= ENSP00000506623.1:n.*711A=
ENST00000679976.1:c.*332A= ENSP00000505565.1:n.*332A=
ENST00000680166.1:n.4037A=
ENST00000680517.1:c.*136A= ENSP00000505803.1:n.*136A=
ENST00000680582.1:n.1710A=
ENST00000680613.1:c.*119A= ENSP00000506114.1:n.*119A=
ENST00000680662.1:c.*662A= ENSP00000505080.1:n.*662A=
ENST00000680691.1:c.*411A= ENSP00000506487.1:n.*411A=
ENST00000680694.1:c.*336A= ENSP00000505658.1:n.*336A=
ENST00000680743.1:c.*415A= ENSP00000505073.1:n.*415A=
ENST00000680749.1:c.*33A= ENSP00000505122.1:n.*33A=
ENST00000680798.1:c.*223A= ENSP00000505670.1:n.*223A=
ENST00000680805.1:c.709-993A= ENSP00000505447.1:n.709-993A=
ENST00000680844.1:c.*532A= ENSP00000506541.1:n.*532A=
ENST00000680948.1:c.*615A= ENSP00000505441.1:n.*615A=
ENST00000680964.1:c.748A= ENSP00000505961.1:p.Ile250=
ENST00000681037.1:c.*2232A= ENSP00000506025.1:n.*2232A=
ENST00000681063.1:c.600-993A= ENSP00000506616.1:n.600-993A=
ENST00000681209.1:c.*403A= ENSP00000505877.1:n.*403A=
ENST00000681278.1:n.1105A=
ENST00000681289.1:n.4743A=
ENST00000681361.1:c.*415A= ENSP00000506679.1:n.*415A=
ENST00000681430.1:c.748A= ENSP00000506301.1:p.Ile250=
ENST00000681446.1:c.*330A= ENSP00000506244.1:n.*330A=
ENST00000681450.1:c.*419A= ENSP00000505660.1:n.*419A=
ENST00000681548.1:c.*334A= ENSP00000505275.1:n.*334A=
ENST00000681616.1:c.*407A= ENSP00000505111.1:n.*407A=
ENST00000681621.1:c.*332A= ENSP00000505770.1:n.*332A=
ENST00000681680.1:n.2843A=
ENST00000681720.1:c.*203A= ENSP00000505438.1:n.*203A=
ENST00000681730.1:n.970A=
ENST00000681790.1:c.490A= ENSP00000505130.1:p.Ile164=
ENST00000681837.1:n.1364A=
ENST00000681913.1:n.2872A=
ENST00000681916.1:c.*516A= ENSP00000506477.1:n.*516A=
ENST00000681930.1:n.2872A=
ENST00000370834.9:c.847A= ENSP00000359871.5:p.Ile283=
ENST00000370841.8:c.748A= ENSP00000359878.4:p.Ile250=
ENST00000420607.6:c.760A= ENSP00000409612.2:p.Ile254=
ENST00000525808.5:c.*334A= ENSP00000434823.1:n.*334A=
ENST00000526129.5:c.*532A= ENSP00000434092.1:n.*532A=
ENST00000526196.5:c.*516A= ENSP00000431953.1:n.*516A=
ENST00000526930.1:n.521A=
ENST00000529059.5:n.657A=
ENST00000530953.6:c.*245A= ENSP00000431372.1:n.*245A=
ENST00000532207.5:n.478A=
ENST00000532509.5:c.*512A= ENSP00000432522.1:n.*512A=
ENST00000534334.5:c.*332A= ENSP00000435584.1:n.*332A=
ENST00000541113.5:c.640A= ENSP00000442324.1:p.Ile214=
NM_000016.5:c.748A= NP_000007.1:p.Ile250=
NM_001127328.2:c.760A= NP_001120800.1:p.Ile254=
NM_001286042.1:c.640A= NP_001272971.1:p.Ile214=
NM_001286043.1:c.847A= NP_001272972.1:p.Ile283=
NM_001286044.1:c.181A= NP_001272973.1:p.Ile61=
NM_000016.6:c.748A= MANE Select NP_000007.1:p.Ile250=
NM_001127328.3:c.760A= NP_001120800.1:p.Ile254=
NM_001286042.2:c.640A= NP_001272971.1:p.Ile214=
NM_001286043.2:c.847A= NP_001272972.1:p.Ile283=
NM_001286044.2:c.181A= NP_001272973.1:p.Ile61=