Canonical Allele Identifier: CA1176726891
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761366A= , CM000663.2:g.75761366A= GRCh38
NC_000001.10:g.76227051A= , CM000663.1:g.76227051A= GRCh37
NC_000001.9:g.75999639A= NCBI36
NG_007045.2:g.42009A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1190A= MANE Select ENSP00000359878.5:p.Tyr397=
ENST00000473018.3:n.3314A=
ENST00000532207.6:n.2201A=
ENST00000541113.6:c.1094A= ENSP00000442324.2:p.Tyr365=
ENST00000679509.1:n.2152A=
ENST00000679530.1:c.*958A= ENSP00000506454.1:n.*958A=
ENST00000679615.1:n.3205A=
ENST00000679687.1:c.752A= ENSP00000506598.1:p.Tyr251=
ENST00000679704.1:c.*956A= ENSP00000505117.1:n.*956A=
ENST00000679709.1:c.*1153A= ENSP00000506623.1:n.*1153A=
ENST00000679976.1:c.*774A= ENSP00000505565.1:n.*774A=
ENST00000680166.1:n.4479A=
ENST00000680315.1:n.1073A=
ENST00000680517.1:c.*578A= ENSP00000505803.1:n.*578A=
ENST00000680582.1:n.2152A=
ENST00000680613.1:c.*683A= ENSP00000506114.1:n.*683A=
ENST00000680662.1:c.*1104A= ENSP00000505080.1:n.*1104A=
ENST00000680691.1:c.*853A= ENSP00000506487.1:n.*853A=
ENST00000680694.1:c.*778A= ENSP00000505658.1:n.*778A=
ENST00000680743.1:c.*979A= ENSP00000505073.1:n.*979A=
ENST00000680749.1:c.*475A= ENSP00000505122.1:n.*475A=
ENST00000680798.1:c.*665A= ENSP00000505670.1:n.*665A=
ENST00000680805.1:c.1049A= ENSP00000505447.1:p.Tyr350=
ENST00000680844.1:c.*974A= ENSP00000506541.1:n.*974A=
ENST00000680948.1:c.*1057A= ENSP00000505441.1:n.*1057A=
ENST00000680964.1:c.*283A= ENSP00000505961.1:n.*283A=
ENST00000681037.1:c.*2674A= ENSP00000506025.1:n.*2674A=
ENST00000681063.1:c.*459A= ENSP00000506616.1:n.*459A=
ENST00000681209.1:c.*845A= ENSP00000505877.1:n.*845A=
ENST00000681278.1:n.1892A=
ENST00000681289.1:n.5185A=
ENST00000681361.1:c.*857A= ENSP00000506679.1:n.*857A=
ENST00000681430.1:c.*283A= ENSP00000506301.1:n.*283A=
ENST00000681446.1:c.*894A= ENSP00000506244.1:n.*894A=
ENST00000681450.1:c.*861A= ENSP00000505660.1:n.*861A=
ENST00000681548.1:c.*776A= ENSP00000505275.1:n.*776A=
ENST00000681616.1:c.*849A= ENSP00000505111.1:n.*849A=
ENST00000681621.1:c.*774A= ENSP00000505770.1:n.*774A=
ENST00000681680.1:n.3285A=
ENST00000681720.1:c.*645A= ENSP00000505438.1:n.*645A=
ENST00000681730.1:n.1412A=
ENST00000681790.1:c.932A= ENSP00000505130.1:p.Tyr311=
ENST00000681837.1:n.1806A=
ENST00000681913.1:n.3436A=
ENST00000681916.1:c.*958A= ENSP00000506477.1:n.*958A=
ENST00000681930.1:n.3314A=
ENST00000370834.9:c.1289A= ENSP00000359871.5:p.Tyr430=
ENST00000370841.8:c.1190A= ENSP00000359878.4:p.Tyr397=
ENST00000420607.6:c.1202A= ENSP00000409612.2:p.Tyr401=
ENST00000481374.1:n.463A=
ENST00000525808.5:c.*776A= ENSP00000434823.1:n.*776A=
ENST00000526129.5:c.*974A= ENSP00000434092.1:n.*974A=
ENST00000526196.5:c.*958A= ENSP00000431953.1:n.*958A=
ENST00000528016.1:c.160-7811A= ENSP00000434284.1:n.160-7811A=
ENST00000529059.5:n.1099A=
ENST00000541113.5:c.1082A= ENSP00000442324.1:p.Tyr361=
NM_000016.5:c.1190A= NP_000007.1:p.Tyr397=
NM_001127328.2:c.1202A= NP_001120800.1:p.Tyr401=
NM_001286042.1:c.1082A= NP_001272971.1:p.Tyr361=
NM_001286043.1:c.1289A= NP_001272972.1:p.Tyr430=
NM_001286044.1:c.623A= NP_001272973.1:p.Tyr208=
NM_000016.6:c.1190A= MANE Select NP_000007.1:p.Tyr397=
NM_001127328.3:c.1202A= NP_001120800.1:p.Tyr401=
NM_001286042.2:c.1082A= NP_001272971.1:p.Tyr361=
NM_001286043.2:c.1289A= NP_001272972.1:p.Tyr430=
NM_001286044.2:c.623A= NP_001272973.1:p.Tyr208=