Canonical Allele Identifier: CA1141090409
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740000T= , CM000663.2:g.75740000T= GRCh38
NC_000001.10:g.76205685T= , CM000663.1:g.76205685T= GRCh37
NC_000001.9:g.75978273T= NCBI36
NG_007045.2:g.20643T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.489T= MANE Select ENSP00000359878.5:p.Pro163=
ENST00000473018.3:n.2613T=
ENST00000541113.6:c.489T= ENSP00000442324.2:p.Pro163=
ENST00000679509.1:n.1451T=
ENST00000679530.1:c.*257T= ENSP00000506454.1:n.*257T=
ENST00000679615.1:n.2613T=
ENST00000679687.1:c.51T= ENSP00000506598.1:p.Pro17=
ENST00000679704.1:c.*255T= ENSP00000505117.1:n.*255T=
ENST00000679709.1:c.*452T= ENSP00000506623.1:n.*452T=
ENST00000679804.1:n.228T=
ENST00000679976.1:c.*73T= ENSP00000505565.1:n.*73T=
ENST00000680166.1:n.3778T=
ENST00000680517.1:c.307T= ENSP00000505803.1:p.Trp103=
ENST00000680582.1:n.1451T=
ENST00000680613.1:c.489T= ENSP00000506114.1:p.Pro163=
ENST00000680662.1:c.*403T= ENSP00000505080.1:n.*403T=
ENST00000680691.1:c.*152T= ENSP00000506487.1:n.*152T=
ENST00000680694.1:c.*77T= ENSP00000505658.1:n.*77T=
ENST00000680743.1:c.*156T= ENSP00000505073.1:n.*156T=
ENST00000680749.1:c.489T= ENSP00000505122.1:p.Pro163=
ENST00000680798.1:c.*73T= ENSP00000505670.1:n.*73T=
ENST00000680805.1:c.489T= ENSP00000505447.1:p.Pro163=
ENST00000680844.1:c.*273T= ENSP00000506541.1:n.*273T=
ENST00000680948.1:c.*356T= ENSP00000505441.1:n.*356T=
ENST00000680964.1:c.489T= ENSP00000505961.1:p.Pro163=
ENST00000681037.1:c.489T= ENSP00000506025.1:p.Pro163=
ENST00000681063.1:c.489T= ENSP00000506616.1:p.Pro163=
ENST00000681209.1:c.*253T= ENSP00000505877.1:n.*253T=
ENST00000681278.1:n.846T=
ENST00000681289.1:n.846T=
ENST00000681361.1:c.*156T= ENSP00000506679.1:n.*156T=
ENST00000681430.1:c.489T= ENSP00000506301.1:p.Pro163=
ENST00000681446.1:c.*71T= ENSP00000506244.1:n.*71T=
ENST00000681450.1:c.*160T= ENSP00000505660.1:n.*160T=
ENST00000681548.1:c.*75T= ENSP00000505275.1:n.*75T=
ENST00000681616.1:c.*257T= ENSP00000505111.1:n.*257T=
ENST00000681621.1:c.*73T= ENSP00000505770.1:n.*73T=
ENST00000681680.1:n.2613T=
ENST00000681720.1:c.*55-5806T= ENSP00000505438.1:n.*55-5806T=
ENST00000681730.1:n.711T=
ENST00000681790.1:c.231T= ENSP00000505130.1:p.Pro77=
ENST00000681837.1:n.1105T=
ENST00000681913.1:n.2613T=
ENST00000681916.1:c.*257T= ENSP00000506477.1:n.*257T=
ENST00000681930.1:n.2613T=
ENST00000370834.9:c.588T= ENSP00000359871.5:p.Pro196=
ENST00000370841.8:c.489T= ENSP00000359878.4:p.Pro163=
ENST00000420607.6:c.501T= ENSP00000409612.2:p.Pro167=
ENST00000525808.5:c.*75T= ENSP00000434823.1:n.*75T=
ENST00000526129.5:c.*273T= ENSP00000434092.1:n.*273T=
ENST00000526196.5:c.*257T= ENSP00000431953.1:n.*257T=
ENST00000526930.1:n.262T=
ENST00000529059.5:n.398T=
ENST00000530953.6:c.139T= ENSP00000431372.1:p.Trp47=
ENST00000532509.5:c.*253T= ENSP00000432522.1:n.*253T=
ENST00000534334.5:c.*73T= ENSP00000435584.1:n.*73T=
ENST00000541113.5:c.381T= ENSP00000442324.1:p.Pro127=
NM_000016.5:c.489T= NP_000007.1:p.Pro163=
NM_001127328.2:c.501T= NP_001120800.1:p.Pro167=
NM_001286042.1:c.381T= NP_001272971.1:p.Pro127=
NM_001286043.1:c.588T= NP_001272972.1:p.Pro196=
NM_001286044.1:c.-79T= NP_001272973.1:n.-79T=
NM_000016.6:c.489T= MANE Select NP_000007.1:p.Pro163=
NM_001127328.3:c.501T= NP_001120800.1:p.Pro167=
NM_001286042.2:c.381T= NP_001272971.1:p.Pro127=
NM_001286043.2:c.588T= NP_001272972.1:p.Pro196=
NM_001286044.2:c.-79T= NP_001272973.1:n.-79T=