Canonical Allele Identifier: CA340818093

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226925C>G (hg19) ; chr1:g.75761240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761240C>G , CM000663.2:g.75761240C>G	GRCh38
NC_000001.10:g.76226925C>G , CM000663.1:g.76226925C>G	GRCh37
NC_000001.9:g.75999513C>G	NCBI36
NG_007045.2:g.41883C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1064C>G MANE Select	ENSP00000359878.5:p.Ser355Cys
ENST00000473018.3:n.3188C>G
ENST00000532207.6:n.2075C>G
ENST00000541113.6:c.968C>G	ENSP00000442324.2:p.Ser323Cys
ENST00000679509.1:n.2026C>G
ENST00000679530.1:c.*832C>G	ENSP00000506454.1:n.*832C>G
ENST00000679615.1:n.3079C>G
ENST00000679687.1:c.626C>G	ENSP00000506598.1:p.Ser209Cys
ENST00000679704.1:c.*830C>G	ENSP00000505117.1:n.*830C>G
ENST00000679709.1:c.*1027C>G	ENSP00000506623.1:n.*1027C>G
ENST00000679976.1:c.*648C>G	ENSP00000505565.1:n.*648C>G
ENST00000680166.1:n.4353C>G
ENST00000680315.1:n.947C>G
ENST00000680517.1:c.*452C>G	ENSP00000505803.1:n.*452C>G
ENST00000680582.1:n.2026C>G
ENST00000680613.1:c.*557C>G	ENSP00000506114.1:n.*557C>G
ENST00000680662.1:c.*978C>G	ENSP00000505080.1:n.*978C>G
ENST00000680691.1:c.*727C>G	ENSP00000506487.1:n.*727C>G
ENST00000680694.1:c.*652C>G	ENSP00000505658.1:n.*652C>G
ENST00000680743.1:c.*853C>G	ENSP00000505073.1:n.*853C>G
ENST00000680749.1:c.*349C>G	ENSP00000505122.1:n.*349C>G
ENST00000680798.1:c.*539C>G	ENSP00000505670.1:n.*539C>G
ENST00000680805.1:c.923C>G	ENSP00000505447.1:p.Ser308Cys
ENST00000680844.1:c.*848C>G	ENSP00000506541.1:n.*848C>G
ENST00000680948.1:c.*931C>G	ENSP00000505441.1:n.*931C>G
ENST00000680964.1:c.*157C>G	ENSP00000505961.1:n.*157C>G
ENST00000681037.1:c.*2548C>G	ENSP00000506025.1:n.*2548C>G
ENST00000681063.1:c.*333C>G	ENSP00000506616.1:n.*333C>G
ENST00000681209.1:c.*719C>G	ENSP00000505877.1:n.*719C>G
ENST00000681278.1:n.1766C>G
ENST00000681289.1:n.5059C>G
ENST00000681361.1:c.*731C>G	ENSP00000506679.1:n.*731C>G
ENST00000681430.1:c.*157C>G	ENSP00000506301.1:n.*157C>G
ENST00000681446.1:c.*768C>G	ENSP00000506244.1:n.*768C>G
ENST00000681450.1:c.*735C>G	ENSP00000505660.1:n.*735C>G
ENST00000681548.1:c.*650C>G	ENSP00000505275.1:n.*650C>G
ENST00000681616.1:c.*723C>G	ENSP00000505111.1:n.*723C>G
ENST00000681621.1:c.*648C>G	ENSP00000505770.1:n.*648C>G
ENST00000681680.1:n.3159C>G
ENST00000681720.1:c.*519C>G	ENSP00000505438.1:n.*519C>G
ENST00000681730.1:n.1286C>G
ENST00000681790.1:c.806C>G	ENSP00000505130.1:p.Ser269Cys
ENST00000681837.1:n.1680C>G
ENST00000681913.1:n.3310C>G
ENST00000681916.1:c.*832C>G	ENSP00000506477.1:n.*832C>G
ENST00000681930.1:n.3188C>G
ENST00000370834.9:c.1163C>G	ENSP00000359871.5:p.Ser388Cys
ENST00000370841.8:c.1064C>G	ENSP00000359878.4:p.Ser355Cys
ENST00000420607.6:c.1076C>G	ENSP00000409612.2:p.Ser359Cys
ENST00000481374.1:n.337C>G
ENST00000525808.5:c.*650C>G	ENSP00000434823.1:n.*650C>G
ENST00000526129.5:c.*848C>G	ENSP00000434092.1:n.*848C>G
ENST00000526196.5:c.*832C>G	ENSP00000431953.1:n.*832C>G
ENST00000528016.1:c.160-7937C>G	ENSP00000434284.1:n.160-7937C>G
ENST00000529059.5:n.973C>G
ENST00000534334.5:c.*805C>G	ENSP00000435584.1:n.*805C>G
ENST00000541113.5:c.956C>G	ENSP00000442324.1:p.Ser319Cys
NM_000016.5:c.1064C>G	NP_000007.1:p.Ser355Cys
NM_001127328.2:c.1076C>G	NP_001120800.1:p.Ser359Cys
NM_001286042.1:c.956C>G	NP_001272971.1:p.Ser319Cys
NM_001286043.1:c.1163C>G	NP_001272972.1:p.Ser388Cys
NM_001286044.1:c.497C>G	NP_001272973.1:p.Ser166Cys
NM_000016.6:c.1064C>G MANE Select	NP_000007.1:p.Ser355Cys
NM_001127328.3:c.1076C>G	NP_001120800.1:p.Ser359Cys
NM_001286042.2:c.956C>G	NP_001272971.1:p.Ser319Cys
NM_001286043.2:c.1163C>G	NP_001272972.1:p.Ser388Cys
NM_001286044.2:c.497C>G	NP_001272973.1:p.Ser166Cys