Canonical Allele Identifier: CA1176726860
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761266A= , CM000663.2:g.75761266A= GRCh38
NC_000001.10:g.76226951A= , CM000663.1:g.76226951A= GRCh37
NC_000001.9:g.75999539A= NCBI36
NG_007045.2:g.41909A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1090A= MANE Select ENSP00000359878.5:p.Ile364=
ENST00000473018.3:n.3214A=
ENST00000532207.6:n.2101A=
ENST00000541113.6:c.994A= ENSP00000442324.2:p.Ile332=
ENST00000679509.1:n.2052A=
ENST00000679530.1:c.*858A= ENSP00000506454.1:n.*858A=
ENST00000679615.1:n.3105A=
ENST00000679687.1:c.652A= ENSP00000506598.1:p.Ile218=
ENST00000679704.1:c.*856A= ENSP00000505117.1:n.*856A=
ENST00000679709.1:c.*1053A= ENSP00000506623.1:n.*1053A=
ENST00000679976.1:c.*674A= ENSP00000505565.1:n.*674A=
ENST00000680166.1:n.4379A=
ENST00000680315.1:n.973A=
ENST00000680517.1:c.*478A= ENSP00000505803.1:n.*478A=
ENST00000680582.1:n.2052A=
ENST00000680613.1:c.*583A= ENSP00000506114.1:n.*583A=
ENST00000680662.1:c.*1004A= ENSP00000505080.1:n.*1004A=
ENST00000680691.1:c.*753A= ENSP00000506487.1:n.*753A=
ENST00000680694.1:c.*678A= ENSP00000505658.1:n.*678A=
ENST00000680743.1:c.*879A= ENSP00000505073.1:n.*879A=
ENST00000680749.1:c.*375A= ENSP00000505122.1:n.*375A=
ENST00000680798.1:c.*565A= ENSP00000505670.1:n.*565A=
ENST00000680805.1:c.949A= ENSP00000505447.1:p.Ile317=
ENST00000680844.1:c.*874A= ENSP00000506541.1:n.*874A=
ENST00000680948.1:c.*957A= ENSP00000505441.1:n.*957A=
ENST00000680964.1:c.*183A= ENSP00000505961.1:n.*183A=
ENST00000681037.1:c.*2574A= ENSP00000506025.1:n.*2574A=
ENST00000681063.1:c.*359A= ENSP00000506616.1:n.*359A=
ENST00000681209.1:c.*745A= ENSP00000505877.1:n.*745A=
ENST00000681278.1:n.1792A=
ENST00000681289.1:n.5085A=
ENST00000681361.1:c.*757A= ENSP00000506679.1:n.*757A=
ENST00000681430.1:c.*183A= ENSP00000506301.1:n.*183A=
ENST00000681446.1:c.*794A= ENSP00000506244.1:n.*794A=
ENST00000681450.1:c.*761A= ENSP00000505660.1:n.*761A=
ENST00000681548.1:c.*676A= ENSP00000505275.1:n.*676A=
ENST00000681616.1:c.*749A= ENSP00000505111.1:n.*749A=
ENST00000681621.1:c.*674A= ENSP00000505770.1:n.*674A=
ENST00000681680.1:n.3185A=
ENST00000681720.1:c.*545A= ENSP00000505438.1:n.*545A=
ENST00000681730.1:n.1312A=
ENST00000681790.1:c.832A= ENSP00000505130.1:p.Ile278=
ENST00000681837.1:n.1706A=
ENST00000681913.1:n.3336A=
ENST00000681916.1:c.*858A= ENSP00000506477.1:n.*858A=
ENST00000681930.1:n.3214A=
ENST00000370834.9:c.1189A= ENSP00000359871.5:p.Ile397=
ENST00000370841.8:c.1090A= ENSP00000359878.4:p.Ile364=
ENST00000420607.6:c.1102A= ENSP00000409612.2:p.Ile368=
ENST00000481374.1:n.363A=
ENST00000525808.5:c.*676A= ENSP00000434823.1:n.*676A=
ENST00000526129.5:c.*874A= ENSP00000434092.1:n.*874A=
ENST00000526196.5:c.*858A= ENSP00000431953.1:n.*858A=
ENST00000528016.1:c.160-7911A= ENSP00000434284.1:n.160-7911A=
ENST00000529059.5:n.999A=
ENST00000541113.5:c.982A= ENSP00000442324.1:p.Ile328=
NM_000016.5:c.1090A= NP_000007.1:p.Ile364=
NM_001127328.2:c.1102A= NP_001120800.1:p.Ile368=
NM_001286042.1:c.982A= NP_001272971.1:p.Ile328=
NM_001286043.1:c.1189A= NP_001272972.1:p.Ile397=
NM_001286044.1:c.523A= NP_001272973.1:p.Ile175=
NM_000016.6:c.1090A= MANE Select NP_000007.1:p.Ile364=
NM_001127328.3:c.1102A= NP_001120800.1:p.Ile368=
NM_001286042.2:c.982A= NP_001272971.1:p.Ile328=
NM_001286043.2:c.1189A= NP_001272972.1:p.Ile397=
NM_001286044.2:c.523A= NP_001272973.1:p.Ile175=