Canonical Allele Identifier: CA1176726869
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761295G= , CM000663.2:g.75761295G= GRCh38
NC_000001.10:g.76226980G= , CM000663.1:g.76226980G= GRCh37
NC_000001.9:g.75999568G= NCBI36
NG_007045.2:g.41938G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1119G= MANE Select ENSP00000359878.5:p.Val373=
ENST00000473018.3:n.3243G=
ENST00000532207.6:n.2130G=
ENST00000541113.6:c.1023G= ENSP00000442324.2:p.Val341=
ENST00000679509.1:n.2081G=
ENST00000679530.1:c.*887G= ENSP00000506454.1:n.*887G=
ENST00000679615.1:n.3134G=
ENST00000679687.1:c.681G= ENSP00000506598.1:p.Val227=
ENST00000679704.1:c.*885G= ENSP00000505117.1:n.*885G=
ENST00000679709.1:c.*1082G= ENSP00000506623.1:n.*1082G=
ENST00000679976.1:c.*703G= ENSP00000505565.1:n.*703G=
ENST00000680166.1:n.4408G=
ENST00000680315.1:n.1002G=
ENST00000680517.1:c.*507G= ENSP00000505803.1:n.*507G=
ENST00000680582.1:n.2081G=
ENST00000680613.1:c.*612G= ENSP00000506114.1:n.*612G=
ENST00000680662.1:c.*1033G= ENSP00000505080.1:n.*1033G=
ENST00000680691.1:c.*782G= ENSP00000506487.1:n.*782G=
ENST00000680694.1:c.*707G= ENSP00000505658.1:n.*707G=
ENST00000680743.1:c.*908G= ENSP00000505073.1:n.*908G=
ENST00000680749.1:c.*404G= ENSP00000505122.1:n.*404G=
ENST00000680798.1:c.*594G= ENSP00000505670.1:n.*594G=
ENST00000680805.1:c.978G= ENSP00000505447.1:p.Val326=
ENST00000680844.1:c.*903G= ENSP00000506541.1:n.*903G=
ENST00000680948.1:c.*986G= ENSP00000505441.1:n.*986G=
ENST00000680964.1:c.*212G= ENSP00000505961.1:n.*212G=
ENST00000681037.1:c.*2603G= ENSP00000506025.1:n.*2603G=
ENST00000681063.1:c.*388G= ENSP00000506616.1:n.*388G=
ENST00000681209.1:c.*774G= ENSP00000505877.1:n.*774G=
ENST00000681278.1:n.1821G=
ENST00000681289.1:n.5114G=
ENST00000681361.1:c.*786G= ENSP00000506679.1:n.*786G=
ENST00000681430.1:c.*212G= ENSP00000506301.1:n.*212G=
ENST00000681446.1:c.*823G= ENSP00000506244.1:n.*823G=
ENST00000681450.1:c.*790G= ENSP00000505660.1:n.*790G=
ENST00000681548.1:c.*705G= ENSP00000505275.1:n.*705G=
ENST00000681616.1:c.*778G= ENSP00000505111.1:n.*778G=
ENST00000681621.1:c.*703G= ENSP00000505770.1:n.*703G=
ENST00000681680.1:n.3214G=
ENST00000681720.1:c.*574G= ENSP00000505438.1:n.*574G=
ENST00000681730.1:n.1341G=
ENST00000681790.1:c.861G= ENSP00000505130.1:p.Val287=
ENST00000681837.1:n.1735G=
ENST00000681913.1:n.3365G=
ENST00000681916.1:c.*887G= ENSP00000506477.1:n.*887G=
ENST00000681930.1:n.3243G=
ENST00000370834.9:c.1218G= ENSP00000359871.5:p.Val406=
ENST00000370841.8:c.1119G= ENSP00000359878.4:p.Val373=
ENST00000420607.6:c.1131G= ENSP00000409612.2:p.Val377=
ENST00000481374.1:n.392G=
ENST00000525808.5:c.*705G= ENSP00000434823.1:n.*705G=
ENST00000526129.5:c.*903G= ENSP00000434092.1:n.*903G=
ENST00000526196.5:c.*887G= ENSP00000431953.1:n.*887G=
ENST00000528016.1:c.160-7882G= ENSP00000434284.1:n.160-7882G=
ENST00000529059.5:n.1028G=
ENST00000541113.5:c.1011G= ENSP00000442324.1:p.Val337=
NM_000016.5:c.1119G= NP_000007.1:p.Val373=
NM_001127328.2:c.1131G= NP_001120800.1:p.Val377=
NM_001286042.1:c.1011G= NP_001272971.1:p.Val337=
NM_001286043.1:c.1218G= NP_001272972.1:p.Val406=
NM_001286044.1:c.552G= NP_001272973.1:p.Val184=
NM_000016.6:c.1119G= MANE Select NP_000007.1:p.Val373=
NM_001127328.3:c.1131G= NP_001120800.1:p.Val377=
NM_001286042.2:c.1011G= NP_001272971.1:p.Val337=
NM_001286043.2:c.1218G= NP_001272972.1:p.Val406=
NM_001286044.2:c.552G= NP_001272973.1:p.Val184=