Canonical Allele Identifier: CA1141067521
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761161A= , CM000663.2:g.75761161A= GRCh38
NC_000001.10:g.76226846A= , CM000663.1:g.76226846A= GRCh37
NC_000001.9:g.75999434A= NCBI36
NG_007045.2:g.41804A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.985A= MANE Select ENSP00000359878.5:p.Lys329=
ENST00000473018.3:n.3109A=
ENST00000532207.6:n.1996A=
ENST00000541113.6:c.889A= ENSP00000442324.2:p.Lys297=
ENST00000679509.1:n.1947A=
ENST00000679530.1:c.*753A= ENSP00000506454.1:n.*753A=
ENST00000679615.1:n.3000A=
ENST00000679687.1:c.547A= ENSP00000506598.1:p.Lys183=
ENST00000679704.1:c.*751A= ENSP00000505117.1:n.*751A=
ENST00000679709.1:c.*948A= ENSP00000506623.1:n.*948A=
ENST00000679976.1:c.*569A= ENSP00000505565.1:n.*569A=
ENST00000680166.1:n.4274A=
ENST00000680315.1:n.868A=
ENST00000680517.1:c.*373A= ENSP00000505803.1:n.*373A=
ENST00000680582.1:n.1947A=
ENST00000680613.1:c.*478A= ENSP00000506114.1:n.*478A=
ENST00000680662.1:c.*899A= ENSP00000505080.1:n.*899A=
ENST00000680691.1:c.*648A= ENSP00000506487.1:n.*648A=
ENST00000680694.1:c.*573A= ENSP00000505658.1:n.*573A=
ENST00000680743.1:c.*774A= ENSP00000505073.1:n.*774A=
ENST00000680749.1:c.*270A= ENSP00000505122.1:n.*270A=
ENST00000680798.1:c.*460A= ENSP00000505670.1:n.*460A=
ENST00000680805.1:c.844A= ENSP00000505447.1:p.Lys282=
ENST00000680844.1:c.*769A= ENSP00000506541.1:n.*769A=
ENST00000680948.1:c.*852A= ENSP00000505441.1:n.*852A=
ENST00000680964.1:c.*78A= ENSP00000505961.1:n.*78A=
ENST00000681037.1:c.*2469A= ENSP00000506025.1:n.*2469A=
ENST00000681063.1:c.*254A= ENSP00000506616.1:n.*254A=
ENST00000681209.1:c.*640A= ENSP00000505877.1:n.*640A=
ENST00000681278.1:n.1687A=
ENST00000681289.1:n.4980A=
ENST00000681361.1:c.*652A= ENSP00000506679.1:n.*652A=
ENST00000681430.1:c.*78A= ENSP00000506301.1:n.*78A=
ENST00000681446.1:c.*689A= ENSP00000506244.1:n.*689A=
ENST00000681450.1:c.*656A= ENSP00000505660.1:n.*656A=
ENST00000681548.1:c.*571A= ENSP00000505275.1:n.*571A=
ENST00000681616.1:c.*644A= ENSP00000505111.1:n.*644A=
ENST00000681621.1:c.*569A= ENSP00000505770.1:n.*569A=
ENST00000681680.1:n.3080A=
ENST00000681720.1:c.*440A= ENSP00000505438.1:n.*440A=
ENST00000681730.1:n.1207A=
ENST00000681790.1:c.727A= ENSP00000505130.1:p.Lys243=
ENST00000681837.1:n.1601A=
ENST00000681913.1:n.3231A=
ENST00000681916.1:c.*753A= ENSP00000506477.1:n.*753A=
ENST00000681930.1:n.3109A=
ENST00000370834.9:c.1084A= ENSP00000359871.5:p.Lys362=
ENST00000370841.8:c.985A= ENSP00000359878.4:p.Lys329=
ENST00000420607.6:c.997A= ENSP00000409612.2:p.Lys333=
ENST00000481374.1:n.258A=
ENST00000525808.5:c.*571A= ENSP00000434823.1:n.*571A=
ENST00000526129.5:c.*769A= ENSP00000434092.1:n.*769A=
ENST00000526196.5:c.*753A= ENSP00000431953.1:n.*753A=
ENST00000528016.1:c.160-8016A= ENSP00000434284.1:n.160-8016A=
ENST00000529059.5:n.894A=
ENST00000532207.5:n.715A=
ENST00000534334.5:c.*726A= ENSP00000435584.1:n.*726A=
ENST00000541113.5:c.877A= ENSP00000442324.1:p.Lys293=
NM_000016.5:c.985A= NP_000007.1:p.Lys329=
NM_001127328.2:c.997A= NP_001120800.1:p.Lys333=
NM_001286042.1:c.877A= NP_001272971.1:p.Lys293=
NM_001286043.1:c.1084A= NP_001272972.1:p.Lys362=
NM_001286044.1:c.418A= NP_001272973.1:p.Lys140=
NM_000016.6:c.985A= MANE Select NP_000007.1:p.Lys329=
NM_001127328.3:c.997A= NP_001120800.1:p.Lys333=
NM_001286042.2:c.877A= NP_001272971.1:p.Lys293=
NM_001286043.2:c.1084A= NP_001272972.1:p.Lys362=
NM_001286044.2:c.418A= NP_001272973.1:p.Lys140=