Canonical Allele Identifier: CA1176727414
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762727T= , CM000663.2:g.75762727T= GRCh38
NC_000001.10:g.76228412T= , CM000663.1:g.76228412T= GRCh37
NC_000001.9:g.76001000T= NCBI36
NG_007045.2:g.43370T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1230T= MANE Select ENSP00000359878.5:p.Ile410=
ENST00000473018.3:n.3354T=
ENST00000532207.6:n.3562T=
ENST00000541113.6:c.1134T= ENSP00000442324.2:p.Ile378=
ENST00000679509.1:n.3513T=
ENST00000679530.1:c.*998T= ENSP00000506454.1:n.*998T=
ENST00000679615.1:n.4566T=
ENST00000679687.1:c.792T= ENSP00000506598.1:p.Ile264=
ENST00000679704.1:c.*996T= ENSP00000505117.1:n.*996T=
ENST00000679709.1:c.*1193T= ENSP00000506623.1:n.*1193T=
ENST00000679976.1:c.*814T= ENSP00000505565.1:n.*814T=
ENST00000680166.1:n.4519T=
ENST00000680582.1:n.2192T=
ENST00000680613.1:c.*723T= ENSP00000506114.1:n.*723T=
ENST00000680662.1:c.*1144T= ENSP00000505080.1:n.*1144T=
ENST00000680691.1:c.*893T= ENSP00000506487.1:n.*893T=
ENST00000680694.1:c.*818T= ENSP00000505658.1:n.*818T=
ENST00000680743.1:c.*1019T= ENSP00000505073.1:n.*1019T=
ENST00000680749.1:c.*515T= ENSP00000505122.1:n.*515T=
ENST00000680798.1:c.*2026T= ENSP00000505670.1:n.*2026T=
ENST00000680805.1:c.1089T= ENSP00000505447.1:p.Ile363=
ENST00000680844.1:c.*2335T= ENSP00000506541.1:n.*2335T=
ENST00000680948.1:c.*1097T= ENSP00000505441.1:n.*1097T=
ENST00000680964.1:c.*1644T= ENSP00000505961.1:n.*1644T=
ENST00000681037.1:c.*2714T= ENSP00000506025.1:n.*2714T=
ENST00000681063.1:c.*499T= ENSP00000506616.1:n.*499T=
ENST00000681209.1:c.*885T= ENSP00000505877.1:n.*885T=
ENST00000681278.1:n.1932T=
ENST00000681289.1:n.5225T=
ENST00000681361.1:c.*2218T= ENSP00000506679.1:n.*2218T=
ENST00000681430.1:c.*323T= ENSP00000506301.1:n.*323T=
ENST00000681446.1:c.*2255T= ENSP00000506244.1:n.*2255T=
ENST00000681450.1:c.*901T= ENSP00000505660.1:n.*901T=
ENST00000681548.1:c.*2137T= ENSP00000505275.1:n.*2137T=
ENST00000681616.1:c.*2210T= ENSP00000505111.1:n.*2210T=
ENST00000681621.1:c.*2135T= ENSP00000505770.1:n.*2135T=
ENST00000681680.1:n.4646T=
ENST00000681720.1:c.*685T= ENSP00000505438.1:n.*685T=
ENST00000681730.1:n.1452T=
ENST00000681790.1:c.972T= ENSP00000505130.1:p.Ile324=
ENST00000681837.1:n.3167T=
ENST00000681913.1:n.3476T=
ENST00000681916.1:c.*998T= ENSP00000506477.1:n.*998T=
ENST00000681930.1:n.4675T=
ENST00000370834.9:c.1329T= ENSP00000359871.5:p.Ile443=
ENST00000370841.8:c.1230T= ENSP00000359878.4:p.Ile410=
ENST00000420607.6:c.1242T= ENSP00000409612.2:p.Ile414=
ENST00000481374.1:n.468-566T=
ENST00000525808.5:c.*816T= ENSP00000434823.1:n.*816T=
ENST00000526196.5:c.*998T= ENSP00000431953.1:n.*998T=
ENST00000528016.1:c.160-6450T= ENSP00000434284.1:n.160-6450T=
ENST00000529059.5:n.1139T=
ENST00000541113.5:c.1122T= ENSP00000442324.1:p.Ile374=
NM_000016.5:c.1230T= NP_000007.1:p.Ile410=
NM_001127328.2:c.1242T= NP_001120800.1:p.Ile414=
NM_001286042.1:c.1122T= NP_001272971.1:p.Ile374=
NM_001286043.1:c.1329T= NP_001272972.1:p.Ile443=
NM_001286044.1:c.663T= NP_001272973.1:p.Ile221=
NM_000016.6:c.1230T= MANE Select NP_000007.1:p.Ile410=
NM_001127328.3:c.1242T= NP_001120800.1:p.Ile414=
NM_001286042.2:c.1122T= NP_001272971.1:p.Ile374=
NM_001286043.2:c.1329T= NP_001272972.1:p.Ile443=
NM_001286044.2:c.663T= NP_001272973.1:p.Ile221=