Canonical Allele Identifier: CA1176720032
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75745835A= , CM000663.2:g.75745835A= GRCh38
NC_000001.10:g.76211520A= , CM000663.1:g.76211520A= GRCh37
NC_000001.9:g.75984108A= NCBI36
NG_007045.2:g.26478A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.629A= MANE Select ENSP00000359878.5:p.Asp210=
ENST00000473018.3:n.2753A=
ENST00000532207.6:n.1518A=
ENST00000541113.6:c.629A= ENSP00000442324.2:p.Asp210=
ENST00000679509.1:n.1591A=
ENST00000679530.1:c.*397A= ENSP00000506454.1:n.*397A=
ENST00000679615.1:n.2724-3584A=
ENST00000679687.1:c.191A= ENSP00000506598.1:p.Asp64=
ENST00000679704.1:c.*395A= ENSP00000505117.1:n.*395A=
ENST00000679709.1:c.*592A= ENSP00000506623.1:n.*592A=
ENST00000679976.1:c.*213A= ENSP00000505565.1:n.*213A=
ENST00000680166.1:n.3918A=
ENST00000680517.1:c.*97-3584A= ENSP00000505803.1:n.*97-3584A=
ENST00000680582.1:n.1591A=
ENST00000680613.1:c.600A= ENSP00000506114.1:p.Ter200=
ENST00000680662.1:c.*543A= ENSP00000505080.1:n.*543A=
ENST00000680691.1:c.*292A= ENSP00000506487.1:n.*292A=
ENST00000680694.1:c.*217A= ENSP00000505658.1:n.*217A=
ENST00000680743.1:c.*296A= ENSP00000505073.1:n.*296A=
ENST00000680749.1:c.600-3584A= ENSP00000505122.1:n.600-3584A=
ENST00000680798.1:c.*184-3584A= ENSP00000505670.1:n.*184-3584A=
ENST00000680805.1:c.629A= ENSP00000505447.1:p.Asp210=
ENST00000680844.1:c.*413A= ENSP00000506541.1:n.*413A=
ENST00000680948.1:c.*496A= ENSP00000505441.1:n.*496A=
ENST00000680964.1:c.629A= ENSP00000505961.1:p.Asp210=
ENST00000681037.1:c.*2113A= ENSP00000506025.1:n.*2113A=
ENST00000681063.1:c.600-4616A= ENSP00000506616.1:n.600-4616A=
ENST00000681209.1:c.*364-3584A= ENSP00000505877.1:n.*364-3584A=
ENST00000681278.1:n.986A=
ENST00000681289.1:n.4624A=
ENST00000681361.1:c.*296A= ENSP00000506679.1:n.*296A=
ENST00000681430.1:c.629A= ENSP00000506301.1:p.Asp210=
ENST00000681446.1:c.*211A= ENSP00000506244.1:n.*211A=
ENST00000681450.1:c.*300A= ENSP00000505660.1:n.*300A=
ENST00000681548.1:c.*215A= ENSP00000505275.1:n.*215A=
ENST00000681616.1:c.*368-3584A= ENSP00000505111.1:n.*368-3584A=
ENST00000681621.1:c.*213A= ENSP00000505770.1:n.*213A=
ENST00000681680.1:n.2724A=
ENST00000681720.1:c.*84A= ENSP00000505438.1:n.*84A=
ENST00000681730.1:n.851A=
ENST00000681790.1:c.371A= ENSP00000505130.1:p.Asp124=
ENST00000681837.1:n.1245A=
ENST00000681913.1:n.2753A=
ENST00000681916.1:c.*397A= ENSP00000506477.1:n.*397A=
ENST00000681930.1:n.2753A=
ENST00000370834.9:c.728A= ENSP00000359871.5:p.Asp243=
ENST00000370841.8:c.629A= ENSP00000359878.4:p.Asp210=
ENST00000420607.6:c.641A= ENSP00000409612.2:p.Asp214=
ENST00000525808.5:c.*215A= ENSP00000434823.1:n.*215A=
ENST00000526129.5:c.*413A= ENSP00000434092.1:n.*413A=
ENST00000526196.5:c.*397A= ENSP00000431953.1:n.*397A=
ENST00000526930.1:n.402A=
ENST00000529059.5:n.538A=
ENST00000530953.6:c.*126A= ENSP00000431372.1:n.*126A=
ENST00000532207.5:n.359A=
ENST00000532509.5:c.*393A= ENSP00000432522.1:n.*393A=
ENST00000534334.5:c.*213A= ENSP00000435584.1:n.*213A=
ENST00000541113.5:c.521A= ENSP00000442324.1:p.Asp174=
NM_000016.5:c.629A= NP_000007.1:p.Asp210=
NM_001127328.2:c.641A= NP_001120800.1:p.Asp214=
NM_001286042.1:c.521A= NP_001272971.1:p.Asp174=
NM_001286043.1:c.728A= NP_001272972.1:p.Asp243=
NM_001286044.1:c.62A= NP_001272973.1:p.Asp21=
NM_000016.6:c.629A= MANE Select NP_000007.1:p.Asp210=
NM_001127328.3:c.641A= NP_001120800.1:p.Asp214=
NM_001286042.2:c.521A= NP_001272971.1:p.Asp174=
NM_001286043.2:c.728A= NP_001272972.1:p.Asp243=
NM_001286044.2:c.62A= NP_001272973.1:p.Asp21=