Canonical Allele Identifier: CA340818278

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227013A>T (hg19) ; chr1:g.75761328A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761328A>T , CM000663.2:g.75761328A>T	GRCh38
NC_000001.10:g.76227013A>T , CM000663.1:g.76227013A>T	GRCh37
NC_000001.9:g.75999601A>T	NCBI36
NG_007045.2:g.41971A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1152A>T MANE Select	ENSP00000359878.5:p.Glu384Asp
ENST00000473018.3:n.3276A>T
ENST00000532207.6:n.2163A>T
ENST00000541113.6:c.1056A>T	ENSP00000442324.2:p.Glu352Asp
ENST00000679509.1:n.2114A>T
ENST00000679530.1:c.*920A>T	ENSP00000506454.1:n.*920A>T
ENST00000679615.1:n.3167A>T
ENST00000679687.1:c.714A>T	ENSP00000506598.1:p.Glu238Asp
ENST00000679704.1:c.*918A>T	ENSP00000505117.1:n.*918A>T
ENST00000679709.1:c.*1115A>T	ENSP00000506623.1:n.*1115A>T
ENST00000679976.1:c.*736A>T	ENSP00000505565.1:n.*736A>T
ENST00000680166.1:n.4441A>T
ENST00000680315.1:n.1035A>T
ENST00000680517.1:c.*540A>T	ENSP00000505803.1:n.*540A>T
ENST00000680582.1:n.2114A>T
ENST00000680613.1:c.*645A>T	ENSP00000506114.1:n.*645A>T
ENST00000680662.1:c.*1066A>T	ENSP00000505080.1:n.*1066A>T
ENST00000680691.1:c.*815A>T	ENSP00000506487.1:n.*815A>T
ENST00000680694.1:c.*740A>T	ENSP00000505658.1:n.*740A>T
ENST00000680743.1:c.*941A>T	ENSP00000505073.1:n.*941A>T
ENST00000680749.1:c.*437A>T	ENSP00000505122.1:n.*437A>T
ENST00000680798.1:c.*627A>T	ENSP00000505670.1:n.*627A>T
ENST00000680805.1:c.1011A>T	ENSP00000505447.1:p.Glu337Asp
ENST00000680844.1:c.*936A>T	ENSP00000506541.1:n.*936A>T
ENST00000680948.1:c.*1019A>T	ENSP00000505441.1:n.*1019A>T
ENST00000680964.1:c.*245A>T	ENSP00000505961.1:n.*245A>T
ENST00000681037.1:c.*2636A>T	ENSP00000506025.1:n.*2636A>T
ENST00000681063.1:c.*421A>T	ENSP00000506616.1:n.*421A>T
ENST00000681209.1:c.*807A>T	ENSP00000505877.1:n.*807A>T
ENST00000681278.1:n.1854A>T
ENST00000681289.1:n.5147A>T
ENST00000681361.1:c.*819A>T	ENSP00000506679.1:n.*819A>T
ENST00000681430.1:c.*245A>T	ENSP00000506301.1:n.*245A>T
ENST00000681446.1:c.*856A>T	ENSP00000506244.1:n.*856A>T
ENST00000681450.1:c.*823A>T	ENSP00000505660.1:n.*823A>T
ENST00000681548.1:c.*738A>T	ENSP00000505275.1:n.*738A>T
ENST00000681616.1:c.*811A>T	ENSP00000505111.1:n.*811A>T
ENST00000681621.1:c.*736A>T	ENSP00000505770.1:n.*736A>T
ENST00000681680.1:n.3247A>T
ENST00000681720.1:c.*607A>T	ENSP00000505438.1:n.*607A>T
ENST00000681730.1:n.1374A>T
ENST00000681790.1:c.894A>T	ENSP00000505130.1:p.Glu298Asp
ENST00000681837.1:n.1768A>T
ENST00000681913.1:n.3398A>T
ENST00000681916.1:c.*920A>T	ENSP00000506477.1:n.*920A>T
ENST00000681930.1:n.3276A>T
ENST00000370834.9:c.1251A>T	ENSP00000359871.5:p.Glu417Asp
ENST00000370841.8:c.1152A>T	ENSP00000359878.4:p.Glu384Asp
ENST00000420607.6:c.1164A>T	ENSP00000409612.2:p.Glu388Asp
ENST00000481374.1:n.425A>T
ENST00000525808.5:c.*738A>T	ENSP00000434823.1:n.*738A>T
ENST00000526129.5:c.*936A>T	ENSP00000434092.1:n.*936A>T
ENST00000526196.5:c.*920A>T	ENSP00000431953.1:n.*920A>T
ENST00000528016.1:c.160-7849A>T	ENSP00000434284.1:n.160-7849A>T
ENST00000529059.5:n.1061A>T
ENST00000541113.5:c.1044A>T	ENSP00000442324.1:p.Glu348Asp
NM_000016.5:c.1152A>T	NP_000007.1:p.Glu384Asp
NM_001127328.2:c.1164A>T	NP_001120800.1:p.Glu388Asp
NM_001286042.1:c.1044A>T	NP_001272971.1:p.Glu348Asp
NM_001286043.1:c.1251A>T	NP_001272972.1:p.Glu417Asp
NM_001286044.1:c.585A>T	NP_001272973.1:p.Glu195Asp
NM_000016.6:c.1152A>T MANE Select	NP_000007.1:p.Glu384Asp
NM_001127328.3:c.1164A>T	NP_001120800.1:p.Glu388Asp
NM_001286042.2:c.1044A>T	NP_001272971.1:p.Glu348Asp
NM_001286043.2:c.1251A>T	NP_001272972.1:p.Glu417Asp
NM_001286044.2:c.585A>T	NP_001272973.1:p.Glu195Asp