Canonical Allele Identifier: CA1176715651
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740013G= , CM000663.2:g.75740013G= GRCh38
NC_000001.10:g.76205698G= , CM000663.1:g.76205698G= GRCh37
NC_000001.9:g.75978286G= NCBI36
NG_007045.2:g.20656G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.502G= MANE Select ENSP00000359878.5:p.Asp168=
ENST00000473018.3:n.2626G=
ENST00000541113.6:c.502G= ENSP00000442324.2:p.Asp168=
ENST00000679509.1:n.1464G=
ENST00000679530.1:c.*270G= ENSP00000506454.1:n.*270G=
ENST00000679615.1:n.2626G=
ENST00000679687.1:c.64G= ENSP00000506598.1:p.Asp22=
ENST00000679704.1:c.*268G= ENSP00000505117.1:n.*268G=
ENST00000679709.1:c.*465G= ENSP00000506623.1:n.*465G=
ENST00000679804.1:n.241G=
ENST00000679976.1:c.*86G= ENSP00000505565.1:n.*86G=
ENST00000680166.1:n.3791G=
ENST00000680517.1:c.320G= ENSP00000505803.1:p.Ter107=
ENST00000680582.1:n.1464G=
ENST00000680613.1:c.502G= ENSP00000506114.1:p.Asp168=
ENST00000680662.1:c.*416G= ENSP00000505080.1:n.*416G=
ENST00000680691.1:c.*165G= ENSP00000506487.1:n.*165G=
ENST00000680694.1:c.*90G= ENSP00000505658.1:n.*90G=
ENST00000680743.1:c.*169G= ENSP00000505073.1:n.*169G=
ENST00000680749.1:c.502G= ENSP00000505122.1:p.Asp168=
ENST00000680798.1:c.*86G= ENSP00000505670.1:n.*86G=
ENST00000680805.1:c.502G= ENSP00000505447.1:p.Asp168=
ENST00000680844.1:c.*286G= ENSP00000506541.1:n.*286G=
ENST00000680948.1:c.*369G= ENSP00000505441.1:n.*369G=
ENST00000680964.1:c.502G= ENSP00000505961.1:p.Asp168=
ENST00000681037.1:c.502G= ENSP00000506025.1:p.Asp168=
ENST00000681063.1:c.502G= ENSP00000506616.1:p.Asp168=
ENST00000681209.1:c.*266G= ENSP00000505877.1:n.*266G=
ENST00000681278.1:n.859G=
ENST00000681289.1:n.859G=
ENST00000681361.1:c.*169G= ENSP00000506679.1:n.*169G=
ENST00000681430.1:c.502G= ENSP00000506301.1:p.Asp168=
ENST00000681446.1:c.*84G= ENSP00000506244.1:n.*84G=
ENST00000681450.1:c.*173G= ENSP00000505660.1:n.*173G=
ENST00000681548.1:c.*88G= ENSP00000505275.1:n.*88G=
ENST00000681616.1:c.*270G= ENSP00000505111.1:n.*270G=
ENST00000681621.1:c.*86G= ENSP00000505770.1:n.*86G=
ENST00000681680.1:n.2626G=
ENST00000681720.1:c.*55-5793G= ENSP00000505438.1:n.*55-5793G=
ENST00000681730.1:n.724G=
ENST00000681790.1:c.244G= ENSP00000505130.1:p.Asp82=
ENST00000681837.1:n.1118G=
ENST00000681913.1:n.2626G=
ENST00000681916.1:c.*270G= ENSP00000506477.1:n.*270G=
ENST00000681930.1:n.2626G=
ENST00000370834.9:c.601G= ENSP00000359871.5:p.Asp201=
ENST00000370841.8:c.502G= ENSP00000359878.4:p.Asp168=
ENST00000420607.6:c.514G= ENSP00000409612.2:p.Asp172=
ENST00000525808.5:c.*88G= ENSP00000434823.1:n.*88G=
ENST00000526129.5:c.*286G= ENSP00000434092.1:n.*286G=
ENST00000526196.5:c.*270G= ENSP00000431953.1:n.*270G=
ENST00000526930.1:n.275G=
ENST00000529059.5:n.411G=
ENST00000530953.6:c.152G= ENSP00000431372.1:p.Ter51=
ENST00000532509.5:c.*266G= ENSP00000432522.1:n.*266G=
ENST00000534334.5:c.*86G= ENSP00000435584.1:n.*86G=
ENST00000541113.5:c.394G= ENSP00000442324.1:p.Asp132=
NM_000016.5:c.502G= NP_000007.1:p.Asp168=
NM_001127328.2:c.514G= NP_001120800.1:p.Asp172=
NM_001286042.1:c.394G= NP_001272971.1:p.Asp132=
NM_001286043.1:c.601G= NP_001272972.1:p.Asp201=
NM_001286044.1:c.-66G= NP_001272973.1:n.-66G=
NM_000016.6:c.502G= MANE Select NP_000007.1:p.Asp168=
NM_001127328.3:c.514G= NP_001120800.1:p.Asp172=
NM_001286042.2:c.394G= NP_001272971.1:p.Asp132=
NM_001286043.2:c.601G= NP_001272972.1:p.Asp201=
NM_001286044.2:c.-66G= NP_001272973.1:n.-66G=