Canonical Allele Identifier: CA418707608

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226914C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761229C>A , CM000663.2:g.75761229C>A	GRCh38
NC_000001.10:g.76226914C>A , CM000663.1:g.76226914C>A	GRCh37
NC_000001.9:g.75999502C>A	NCBI36
NG_007045.2:g.41872C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1053C>A MANE Select	ENSP00000359878.5:p.Thr351=
ENST00000473018.3:n.3177C>A
ENST00000532207.6:n.2064C>A
ENST00000541113.6:c.957C>A	ENSP00000442324.2:p.Thr319=
ENST00000679509.1:n.2015C>A
ENST00000679530.1:c.*821C>A	ENSP00000506454.1:n.*821C>A
ENST00000679615.1:n.3068C>A
ENST00000679687.1:c.615C>A	ENSP00000506598.1:p.Thr205=
ENST00000679704.1:c.*819C>A	ENSP00000505117.1:n.*819C>A
ENST00000679709.1:c.*1016C>A	ENSP00000506623.1:n.*1016C>A
ENST00000679976.1:c.*637C>A	ENSP00000505565.1:n.*637C>A
ENST00000680166.1:n.4342C>A
ENST00000680315.1:n.936C>A
ENST00000680517.1:c.*441C>A	ENSP00000505803.1:n.*441C>A
ENST00000680582.1:n.2015C>A
ENST00000680613.1:c.*546C>A	ENSP00000506114.1:n.*546C>A
ENST00000680662.1:c.*967C>A	ENSP00000505080.1:n.*967C>A
ENST00000680691.1:c.*716C>A	ENSP00000506487.1:n.*716C>A
ENST00000680694.1:c.*641C>A	ENSP00000505658.1:n.*641C>A
ENST00000680743.1:c.*842C>A	ENSP00000505073.1:n.*842C>A
ENST00000680749.1:c.*338C>A	ENSP00000505122.1:n.*338C>A
ENST00000680798.1:c.*528C>A	ENSP00000505670.1:n.*528C>A
ENST00000680805.1:c.912C>A	ENSP00000505447.1:p.Thr304=
ENST00000680844.1:c.*837C>A	ENSP00000506541.1:n.*837C>A
ENST00000680948.1:c.*920C>A	ENSP00000505441.1:n.*920C>A
ENST00000680964.1:c.*146C>A	ENSP00000505961.1:n.*146C>A
ENST00000681037.1:c.*2537C>A	ENSP00000506025.1:n.*2537C>A
ENST00000681063.1:c.*322C>A	ENSP00000506616.1:n.*322C>A
ENST00000681209.1:c.*708C>A	ENSP00000505877.1:n.*708C>A
ENST00000681278.1:n.1755C>A
ENST00000681289.1:n.5048C>A
ENST00000681361.1:c.*720C>A	ENSP00000506679.1:n.*720C>A
ENST00000681430.1:c.*146C>A	ENSP00000506301.1:n.*146C>A
ENST00000681446.1:c.*757C>A	ENSP00000506244.1:n.*757C>A
ENST00000681450.1:c.*724C>A	ENSP00000505660.1:n.*724C>A
ENST00000681548.1:c.*639C>A	ENSP00000505275.1:n.*639C>A
ENST00000681616.1:c.*712C>A	ENSP00000505111.1:n.*712C>A
ENST00000681621.1:c.*637C>A	ENSP00000505770.1:n.*637C>A
ENST00000681680.1:n.3148C>A
ENST00000681720.1:c.*508C>A	ENSP00000505438.1:n.*508C>A
ENST00000681730.1:n.1275C>A
ENST00000681790.1:c.795C>A	ENSP00000505130.1:p.Thr265=
ENST00000681837.1:n.1669C>A
ENST00000681913.1:n.3299C>A
ENST00000681916.1:c.*821C>A	ENSP00000506477.1:n.*821C>A
ENST00000681930.1:n.3177C>A
ENST00000370834.9:c.1152C>A	ENSP00000359871.5:p.Thr384=
ENST00000370841.8:c.1053C>A	ENSP00000359878.4:p.Thr351=
ENST00000420607.6:c.1065C>A	ENSP00000409612.2:p.Thr355=
ENST00000481374.1:n.326C>A
ENST00000525808.5:c.*639C>A	ENSP00000434823.1:n.*639C>A
ENST00000526129.5:c.*837C>A	ENSP00000434092.1:n.*837C>A
ENST00000526196.5:c.*821C>A	ENSP00000431953.1:n.*821C>A
ENST00000528016.1:c.160-7948C>A	ENSP00000434284.1:n.160-7948C>A
ENST00000529059.5:n.962C>A
ENST00000534334.5:c.*794C>A	ENSP00000435584.1:n.*794C>A
ENST00000541113.5:c.945C>A	ENSP00000442324.1:p.Thr315=
NM_000016.5:c.1053C>A	NP_000007.1:p.Thr351=
NM_001127328.2:c.1065C>A	NP_001120800.1:p.Thr355=
NM_001286042.1:c.945C>A	NP_001272971.1:p.Thr315=
NM_001286043.1:c.1152C>A	NP_001272972.1:p.Thr384=
NM_001286044.1:c.486C>A	NP_001272973.1:p.Thr162=
NM_000016.6:c.1053C>A MANE Select	NP_000007.1:p.Thr351=
NM_001127328.3:c.1065C>A	NP_001120800.1:p.Thr355=
NM_001286042.2:c.945C>A	NP_001272971.1:p.Thr315=
NM_001286043.2:c.1152C>A	NP_001272972.1:p.Thr384=
NM_001286044.2:c.486C>A	NP_001272973.1:p.Thr162=