Canonical Allele Identifier: CA1176721435
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749428A= , CM000663.2:g.75749428A= GRCh38
NC_000001.10:g.76215113A= , CM000663.1:g.76215113A= GRCh37
NC_000001.9:g.75987701A= NCBI36
NG_007045.2:g.30071A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.718A= MANE Select ENSP00000359878.5:p.Met240=
ENST00000473018.3:n.2842A=
ENST00000532207.6:n.1607A=
ENST00000541113.6:c.718A= ENSP00000442324.2:p.Met240=
ENST00000679509.1:n.1680A=
ENST00000679530.1:c.*486A= ENSP00000506454.1:n.*486A=
ENST00000679615.1:n.2733A=
ENST00000679687.1:c.280A= ENSP00000506598.1:p.Met94=
ENST00000679704.1:c.*484A= ENSP00000505117.1:n.*484A=
ENST00000679709.1:c.*681A= ENSP00000506623.1:n.*681A=
ENST00000679976.1:c.*302A= ENSP00000505565.1:n.*302A=
ENST00000680166.1:n.4007A=
ENST00000680517.1:c.*106A= ENSP00000505803.1:n.*106A=
ENST00000680582.1:n.1680A=
ENST00000680613.1:c.*89A= ENSP00000506114.1:n.*89A=
ENST00000680662.1:c.*632A= ENSP00000505080.1:n.*632A=
ENST00000680691.1:c.*381A= ENSP00000506487.1:n.*381A=
ENST00000680694.1:c.*306A= ENSP00000505658.1:n.*306A=
ENST00000680743.1:c.*385A= ENSP00000505073.1:n.*385A=
ENST00000680749.1:c.*3A= ENSP00000505122.1:n.*3A=
ENST00000680798.1:c.*193A= ENSP00000505670.1:n.*193A=
ENST00000680805.1:c.709-1023A= ENSP00000505447.1:n.709-1023A=
ENST00000680844.1:c.*502A= ENSP00000506541.1:n.*502A=
ENST00000680948.1:c.*585A= ENSP00000505441.1:n.*585A=
ENST00000680964.1:c.718A= ENSP00000505961.1:p.Met240=
ENST00000681037.1:c.*2202A= ENSP00000506025.1:n.*2202A=
ENST00000681063.1:c.600-1023A= ENSP00000506616.1:n.600-1023A=
ENST00000681209.1:c.*373A= ENSP00000505877.1:n.*373A=
ENST00000681278.1:n.1075A=
ENST00000681289.1:n.4713A=
ENST00000681361.1:c.*385A= ENSP00000506679.1:n.*385A=
ENST00000681430.1:c.718A= ENSP00000506301.1:p.Met240=
ENST00000681446.1:c.*300A= ENSP00000506244.1:n.*300A=
ENST00000681450.1:c.*389A= ENSP00000505660.1:n.*389A=
ENST00000681548.1:c.*304A= ENSP00000505275.1:n.*304A=
ENST00000681616.1:c.*377A= ENSP00000505111.1:n.*377A=
ENST00000681621.1:c.*302A= ENSP00000505770.1:n.*302A=
ENST00000681680.1:n.2813A=
ENST00000681720.1:c.*173A= ENSP00000505438.1:n.*173A=
ENST00000681730.1:n.940A=
ENST00000681790.1:c.460A= ENSP00000505130.1:p.Met154=
ENST00000681837.1:n.1334A=
ENST00000681913.1:n.2842A=
ENST00000681916.1:c.*486A= ENSP00000506477.1:n.*486A=
ENST00000681930.1:n.2842A=
ENST00000370834.9:c.817A= ENSP00000359871.5:p.Met273=
ENST00000370841.8:c.718A= ENSP00000359878.4:p.Met240=
ENST00000420607.6:c.730A= ENSP00000409612.2:p.Met244=
ENST00000525808.5:c.*304A= ENSP00000434823.1:n.*304A=
ENST00000526129.5:c.*502A= ENSP00000434092.1:n.*502A=
ENST00000526196.5:c.*486A= ENSP00000431953.1:n.*486A=
ENST00000526930.1:n.491A=
ENST00000529059.5:n.627A=
ENST00000530953.6:c.*215A= ENSP00000431372.1:n.*215A=
ENST00000532207.5:n.448A=
ENST00000532509.5:c.*482A= ENSP00000432522.1:n.*482A=
ENST00000534334.5:c.*302A= ENSP00000435584.1:n.*302A=
ENST00000541113.5:c.610A= ENSP00000442324.1:p.Met204=
NM_000016.5:c.718A= NP_000007.1:p.Met240=
NM_001127328.2:c.730A= NP_001120800.1:p.Met244=
NM_001286042.1:c.610A= NP_001272971.1:p.Met204=
NM_001286043.1:c.817A= NP_001272972.1:p.Met273=
NM_001286044.1:c.151A= NP_001272973.1:p.Met51=
NM_000016.6:c.718A= MANE Select NP_000007.1:p.Met240=
NM_001127328.3:c.730A= NP_001120800.1:p.Met244=
NM_001286042.2:c.610A= NP_001272971.1:p.Met204=
NM_001286043.2:c.817A= NP_001272972.1:p.Met273=
NM_001286044.2:c.151A= NP_001272973.1:p.Met51=