Canonical Allele Identifier: CA1176726852
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761245G= , CM000663.2:g.75761245G= GRCh38
NC_000001.10:g.76226930G= , CM000663.1:g.76226930G= GRCh37
NC_000001.9:g.75999518G= NCBI36
NG_007045.2:g.41888G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1069G= MANE Select ENSP00000359878.5:p.Ala357=
ENST00000473018.3:n.3193G=
ENST00000532207.6:n.2080G=
ENST00000541113.6:c.973G= ENSP00000442324.2:p.Ala325=
ENST00000679509.1:n.2031G=
ENST00000679530.1:c.*837G= ENSP00000506454.1:n.*837G=
ENST00000679615.1:n.3084G=
ENST00000679687.1:c.631G= ENSP00000506598.1:p.Ala211=
ENST00000679704.1:c.*835G= ENSP00000505117.1:n.*835G=
ENST00000679709.1:c.*1032G= ENSP00000506623.1:n.*1032G=
ENST00000679976.1:c.*653G= ENSP00000505565.1:n.*653G=
ENST00000680166.1:n.4358G=
ENST00000680315.1:n.952G=
ENST00000680517.1:c.*457G= ENSP00000505803.1:n.*457G=
ENST00000680582.1:n.2031G=
ENST00000680613.1:c.*562G= ENSP00000506114.1:n.*562G=
ENST00000680662.1:c.*983G= ENSP00000505080.1:n.*983G=
ENST00000680691.1:c.*732G= ENSP00000506487.1:n.*732G=
ENST00000680694.1:c.*657G= ENSP00000505658.1:n.*657G=
ENST00000680743.1:c.*858G= ENSP00000505073.1:n.*858G=
ENST00000680749.1:c.*354G= ENSP00000505122.1:n.*354G=
ENST00000680798.1:c.*544G= ENSP00000505670.1:n.*544G=
ENST00000680805.1:c.928G= ENSP00000505447.1:p.Ala310=
ENST00000680844.1:c.*853G= ENSP00000506541.1:n.*853G=
ENST00000680948.1:c.*936G= ENSP00000505441.1:n.*936G=
ENST00000680964.1:c.*162G= ENSP00000505961.1:n.*162G=
ENST00000681037.1:c.*2553G= ENSP00000506025.1:n.*2553G=
ENST00000681063.1:c.*338G= ENSP00000506616.1:n.*338G=
ENST00000681209.1:c.*724G= ENSP00000505877.1:n.*724G=
ENST00000681278.1:n.1771G=
ENST00000681289.1:n.5064G=
ENST00000681361.1:c.*736G= ENSP00000506679.1:n.*736G=
ENST00000681430.1:c.*162G= ENSP00000506301.1:n.*162G=
ENST00000681446.1:c.*773G= ENSP00000506244.1:n.*773G=
ENST00000681450.1:c.*740G= ENSP00000505660.1:n.*740G=
ENST00000681548.1:c.*655G= ENSP00000505275.1:n.*655G=
ENST00000681616.1:c.*728G= ENSP00000505111.1:n.*728G=
ENST00000681621.1:c.*653G= ENSP00000505770.1:n.*653G=
ENST00000681680.1:n.3164G=
ENST00000681720.1:c.*524G= ENSP00000505438.1:n.*524G=
ENST00000681730.1:n.1291G=
ENST00000681790.1:c.811G= ENSP00000505130.1:p.Ala271=
ENST00000681837.1:n.1685G=
ENST00000681913.1:n.3315G=
ENST00000681916.1:c.*837G= ENSP00000506477.1:n.*837G=
ENST00000681930.1:n.3193G=
ENST00000370834.9:c.1168G= ENSP00000359871.5:p.Ala390=
ENST00000370841.8:c.1069G= ENSP00000359878.4:p.Ala357=
ENST00000420607.6:c.1081G= ENSP00000409612.2:p.Ala361=
ENST00000481374.1:n.342G=
ENST00000525808.5:c.*655G= ENSP00000434823.1:n.*655G=
ENST00000526129.5:c.*853G= ENSP00000434092.1:n.*853G=
ENST00000526196.5:c.*837G= ENSP00000431953.1:n.*837G=
ENST00000528016.1:c.160-7932G= ENSP00000434284.1:n.160-7932G=
ENST00000529059.5:n.978G=
ENST00000534334.5:c.*810G= ENSP00000435584.1:n.*810G=
ENST00000541113.5:c.961G= ENSP00000442324.1:p.Ala321=
NM_000016.5:c.1069G= NP_000007.1:p.Ala357=
NM_001127328.2:c.1081G= NP_001120800.1:p.Ala361=
NM_001286042.1:c.961G= NP_001272971.1:p.Ala321=
NM_001286043.1:c.1168G= NP_001272972.1:p.Ala390=
NM_001286044.1:c.502G= NP_001272973.1:p.Ala168=
NM_000016.6:c.1069G= MANE Select NP_000007.1:p.Ala357=
NM_001127328.3:c.1081G= NP_001120800.1:p.Ala361=
NM_001286042.2:c.961G= NP_001272971.1:p.Ala321=
NM_001286043.2:c.1168G= NP_001272972.1:p.Ala390=
NM_001286044.2:c.502G= NP_001272973.1:p.Ala168=