Canonical Allele Identifier: CA418530721

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226836A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761151A>G , CM000663.2:g.75761151A>G	GRCh38
NC_000001.10:g.76226836A>G , CM000663.1:g.76226836A>G	GRCh37
NC_000001.9:g.75999424A>G	NCBI36
NG_007045.2:g.41794A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.975A>G MANE Select	ENSP00000359878.5:p.Glu325=
ENST00000473018.3:n.3099A>G
ENST00000532207.6:n.1986A>G
ENST00000541113.6:c.879A>G	ENSP00000442324.2:p.Glu293=
ENST00000679509.1:n.1937A>G
ENST00000679530.1:c.*743A>G	ENSP00000506454.1:n.*743A>G
ENST00000679615.1:n.2990A>G
ENST00000679687.1:c.537A>G	ENSP00000506598.1:p.Glu179=
ENST00000679704.1:c.*741A>G	ENSP00000505117.1:n.*741A>G
ENST00000679709.1:c.*938A>G	ENSP00000506623.1:n.*938A>G
ENST00000679976.1:c.*559A>G	ENSP00000505565.1:n.*559A>G
ENST00000680166.1:n.4264A>G
ENST00000680315.1:n.858A>G
ENST00000680517.1:c.*363A>G	ENSP00000505803.1:n.*363A>G
ENST00000680582.1:n.1937A>G
ENST00000680613.1:c.*468A>G	ENSP00000506114.1:n.*468A>G
ENST00000680662.1:c.*889A>G	ENSP00000505080.1:n.*889A>G
ENST00000680691.1:c.*638A>G	ENSP00000506487.1:n.*638A>G
ENST00000680694.1:c.*563A>G	ENSP00000505658.1:n.*563A>G
ENST00000680743.1:c.*764A>G	ENSP00000505073.1:n.*764A>G
ENST00000680749.1:c.*260A>G	ENSP00000505122.1:n.*260A>G
ENST00000680798.1:c.*450A>G	ENSP00000505670.1:n.*450A>G
ENST00000680805.1:c.834A>G	ENSP00000505447.1:p.Glu278=
ENST00000680844.1:c.*759A>G	ENSP00000506541.1:n.*759A>G
ENST00000680948.1:c.*842A>G	ENSP00000505441.1:n.*842A>G
ENST00000680964.1:c.*68A>G	ENSP00000505961.1:n.*68A>G
ENST00000681037.1:c.*2459A>G	ENSP00000506025.1:n.*2459A>G
ENST00000681063.1:c.*244A>G	ENSP00000506616.1:n.*244A>G
ENST00000681209.1:c.*630A>G	ENSP00000505877.1:n.*630A>G
ENST00000681278.1:n.1677A>G
ENST00000681289.1:n.4970A>G
ENST00000681361.1:c.*642A>G	ENSP00000506679.1:n.*642A>G
ENST00000681430.1:c.*68A>G	ENSP00000506301.1:n.*68A>G
ENST00000681446.1:c.*679A>G	ENSP00000506244.1:n.*679A>G
ENST00000681450.1:c.*646A>G	ENSP00000505660.1:n.*646A>G
ENST00000681548.1:c.*561A>G	ENSP00000505275.1:n.*561A>G
ENST00000681616.1:c.*634A>G	ENSP00000505111.1:n.*634A>G
ENST00000681621.1:c.*559A>G	ENSP00000505770.1:n.*559A>G
ENST00000681680.1:n.3070A>G
ENST00000681720.1:c.*430A>G	ENSP00000505438.1:n.*430A>G
ENST00000681730.1:n.1197A>G
ENST00000681790.1:c.717A>G	ENSP00000505130.1:p.Glu239=
ENST00000681837.1:n.1591A>G
ENST00000681913.1:n.3221A>G
ENST00000681916.1:c.*743A>G	ENSP00000506477.1:n.*743A>G
ENST00000681930.1:n.3099A>G
ENST00000370834.9:c.1074A>G	ENSP00000359871.5:p.Glu358=
ENST00000370841.8:c.975A>G	ENSP00000359878.4:p.Glu325=
ENST00000420607.6:c.987A>G	ENSP00000409612.2:p.Glu329=
ENST00000481374.1:n.248A>G
ENST00000525808.5:c.*561A>G	ENSP00000434823.1:n.*561A>G
ENST00000526129.5:c.*759A>G	ENSP00000434092.1:n.*759A>G
ENST00000526196.5:c.*743A>G	ENSP00000431953.1:n.*743A>G
ENST00000528016.1:c.160-8026A>G	ENSP00000434284.1:n.160-8026A>G
ENST00000529059.5:n.884A>G
ENST00000532207.5:n.705A>G
ENST00000534334.5:c.*716A>G	ENSP00000435584.1:n.*716A>G
ENST00000541113.5:c.867A>G	ENSP00000442324.1:p.Glu289=
NM_000016.5:c.975A>G	NP_000007.1:p.Glu325=
NM_001127328.2:c.987A>G	NP_001120800.1:p.Glu329=
NM_001286042.1:c.867A>G	NP_001272971.1:p.Glu289=
NM_001286043.1:c.1074A>G	NP_001272972.1:p.Glu358=
NM_001286044.1:c.408A>G	NP_001272973.1:p.Glu136=
NM_000016.6:c.975A>G MANE Select	NP_000007.1:p.Glu325=
NM_001127328.3:c.987A>G	NP_001120800.1:p.Glu329=
NM_001286042.2:c.867A>G	NP_001272971.1:p.Glu289=
NM_001286043.2:c.1074A>G	NP_001272972.1:p.Glu358=
NM_001286044.2:c.408A>G	NP_001272973.1:p.Glu136=