Canonical Allele Identifier: CA418707822

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227043C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761358C>G , CM000663.2:g.75761358C>G	GRCh38
NC_000001.10:g.76227043C>G , CM000663.1:g.76227043C>G	GRCh37
NC_000001.9:g.75999631C>G	NCBI36
NG_007045.2:g.42001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1182C>G MANE Select	ENSP00000359878.5:p.Ala394=
ENST00000473018.3:n.3306C>G
ENST00000532207.6:n.2193C>G
ENST00000541113.6:c.1086C>G	ENSP00000442324.2:p.Ala362=
ENST00000679509.1:n.2144C>G
ENST00000679530.1:c.*950C>G	ENSP00000506454.1:n.*950C>G
ENST00000679615.1:n.3197C>G
ENST00000679687.1:c.744C>G	ENSP00000506598.1:p.Ala248=
ENST00000679704.1:c.*948C>G	ENSP00000505117.1:n.*948C>G
ENST00000679709.1:c.*1145C>G	ENSP00000506623.1:n.*1145C>G
ENST00000679976.1:c.*766C>G	ENSP00000505565.1:n.*766C>G
ENST00000680166.1:n.4471C>G
ENST00000680315.1:n.1065C>G
ENST00000680517.1:c.*570C>G	ENSP00000505803.1:n.*570C>G
ENST00000680582.1:n.2144C>G
ENST00000680613.1:c.*675C>G	ENSP00000506114.1:n.*675C>G
ENST00000680662.1:c.*1096C>G	ENSP00000505080.1:n.*1096C>G
ENST00000680691.1:c.*845C>G	ENSP00000506487.1:n.*845C>G
ENST00000680694.1:c.*770C>G	ENSP00000505658.1:n.*770C>G
ENST00000680743.1:c.*971C>G	ENSP00000505073.1:n.*971C>G
ENST00000680749.1:c.*467C>G	ENSP00000505122.1:n.*467C>G
ENST00000680798.1:c.*657C>G	ENSP00000505670.1:n.*657C>G
ENST00000680805.1:c.1041C>G	ENSP00000505447.1:p.Ala347=
ENST00000680844.1:c.*966C>G	ENSP00000506541.1:n.*966C>G
ENST00000680948.1:c.*1049C>G	ENSP00000505441.1:n.*1049C>G
ENST00000680964.1:c.*275C>G	ENSP00000505961.1:n.*275C>G
ENST00000681037.1:c.*2666C>G	ENSP00000506025.1:n.*2666C>G
ENST00000681063.1:c.*451C>G	ENSP00000506616.1:n.*451C>G
ENST00000681209.1:c.*837C>G	ENSP00000505877.1:n.*837C>G
ENST00000681278.1:n.1884C>G
ENST00000681289.1:n.5177C>G
ENST00000681361.1:c.*849C>G	ENSP00000506679.1:n.*849C>G
ENST00000681430.1:c.*275C>G	ENSP00000506301.1:n.*275C>G
ENST00000681446.1:c.*886C>G	ENSP00000506244.1:n.*886C>G
ENST00000681450.1:c.*853C>G	ENSP00000505660.1:n.*853C>G
ENST00000681548.1:c.*768C>G	ENSP00000505275.1:n.*768C>G
ENST00000681616.1:c.*841C>G	ENSP00000505111.1:n.*841C>G
ENST00000681621.1:c.*766C>G	ENSP00000505770.1:n.*766C>G
ENST00000681680.1:n.3277C>G
ENST00000681720.1:c.*637C>G	ENSP00000505438.1:n.*637C>G
ENST00000681730.1:n.1404C>G
ENST00000681790.1:c.924C>G	ENSP00000505130.1:p.Ala308=
ENST00000681837.1:n.1798C>G
ENST00000681913.1:n.3428C>G
ENST00000681916.1:c.*950C>G	ENSP00000506477.1:n.*950C>G
ENST00000681930.1:n.3306C>G
ENST00000370834.9:c.1281C>G	ENSP00000359871.5:p.Ala427=
ENST00000370841.8:c.1182C>G	ENSP00000359878.4:p.Ala394=
ENST00000420607.6:c.1194C>G	ENSP00000409612.2:p.Ala398=
ENST00000481374.1:n.455C>G
ENST00000525808.5:c.*768C>G	ENSP00000434823.1:n.*768C>G
ENST00000526129.5:c.*966C>G	ENSP00000434092.1:n.*966C>G
ENST00000526196.5:c.*950C>G	ENSP00000431953.1:n.*950C>G
ENST00000528016.1:c.160-7819C>G	ENSP00000434284.1:n.160-7819C>G
ENST00000529059.5:n.1091C>G
ENST00000541113.5:c.1074C>G	ENSP00000442324.1:p.Ala358=
NM_000016.5:c.1182C>G	NP_000007.1:p.Ala394=
NM_001127328.2:c.1194C>G	NP_001120800.1:p.Ala398=
NM_001286042.1:c.1074C>G	NP_001272971.1:p.Ala358=
NM_001286043.1:c.1281C>G	NP_001272972.1:p.Ala427=
NM_001286044.1:c.615C>G	NP_001272973.1:p.Ala205=
NM_000016.6:c.1182C>G MANE Select	NP_000007.1:p.Ala394=
NM_001127328.3:c.1194C>G	NP_001120800.1:p.Ala398=
NM_001286042.2:c.1074C>G	NP_001272971.1:p.Ala358=
NM_001286043.2:c.1281C>G	NP_001272972.1:p.Ala427=
NM_001286044.2:c.615C>G	NP_001272973.1:p.Ala205=