Canonical Allele Identifier: CA340817836

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226808A>G (hg19) ; chr1:g.75761123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761123A>G , CM000663.2:g.75761123A>G	GRCh38
NC_000001.10:g.76226808A>G , CM000663.1:g.76226808A>G	GRCh37
NC_000001.9:g.75999396A>G	NCBI36
NG_007045.2:g.41766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.947A>G MANE Select	ENSP00000359878.5:p.His316Arg
ENST00000473018.3:n.3071A>G
ENST00000532207.6:n.1958A>G
ENST00000541113.6:c.851A>G	ENSP00000442324.2:p.His284Arg
ENST00000679509.1:n.1909A>G
ENST00000679530.1:c.*715A>G	ENSP00000506454.1:n.*715A>G
ENST00000679615.1:n.2962A>G
ENST00000679687.1:c.509A>G	ENSP00000506598.1:p.His170Arg
ENST00000679704.1:c.*713A>G	ENSP00000505117.1:n.*713A>G
ENST00000679709.1:c.*910A>G	ENSP00000506623.1:n.*910A>G
ENST00000679976.1:c.*531A>G	ENSP00000505565.1:n.*531A>G
ENST00000680166.1:n.4236A>G
ENST00000680315.1:n.830A>G
ENST00000680517.1:c.*335A>G	ENSP00000505803.1:n.*335A>G
ENST00000680582.1:n.1909A>G
ENST00000680613.1:c.*440A>G	ENSP00000506114.1:n.*440A>G
ENST00000680662.1:c.*861A>G	ENSP00000505080.1:n.*861A>G
ENST00000680691.1:c.*610A>G	ENSP00000506487.1:n.*610A>G
ENST00000680694.1:c.*535A>G	ENSP00000505658.1:n.*535A>G
ENST00000680743.1:c.*736A>G	ENSP00000505073.1:n.*736A>G
ENST00000680749.1:c.*232A>G	ENSP00000505122.1:n.*232A>G
ENST00000680798.1:c.*422A>G	ENSP00000505670.1:n.*422A>G
ENST00000680805.1:c.806A>G	ENSP00000505447.1:p.His269Arg
ENST00000680844.1:c.*731A>G	ENSP00000506541.1:n.*731A>G
ENST00000680948.1:c.*814A>G	ENSP00000505441.1:n.*814A>G
ENST00000680964.1:c.*40A>G	ENSP00000505961.1:n.*40A>G
ENST00000681037.1:c.*2431A>G	ENSP00000506025.1:n.*2431A>G
ENST00000681063.1:c.*216A>G	ENSP00000506616.1:n.*216A>G
ENST00000681209.1:c.*602A>G	ENSP00000505877.1:n.*602A>G
ENST00000681278.1:n.1649A>G
ENST00000681289.1:n.4942A>G
ENST00000681361.1:c.*614A>G	ENSP00000506679.1:n.*614A>G
ENST00000681430.1:c.*40A>G	ENSP00000506301.1:n.*40A>G
ENST00000681446.1:c.*651A>G	ENSP00000506244.1:n.*651A>G
ENST00000681450.1:c.*618A>G	ENSP00000505660.1:n.*618A>G
ENST00000681548.1:c.*533A>G	ENSP00000505275.1:n.*533A>G
ENST00000681616.1:c.*606A>G	ENSP00000505111.1:n.*606A>G
ENST00000681621.1:c.*531A>G	ENSP00000505770.1:n.*531A>G
ENST00000681680.1:n.3042A>G
ENST00000681720.1:c.*402A>G	ENSP00000505438.1:n.*402A>G
ENST00000681730.1:n.1169A>G
ENST00000681790.1:c.689A>G	ENSP00000505130.1:p.His230Arg
ENST00000681837.1:n.1563A>G
ENST00000681913.1:n.3193A>G
ENST00000681916.1:c.*715A>G	ENSP00000506477.1:n.*715A>G
ENST00000681930.1:n.3071A>G
ENST00000370834.9:c.1046A>G	ENSP00000359871.5:p.His349Arg
ENST00000370841.8:c.947A>G	ENSP00000359878.4:p.His316Arg
ENST00000420607.6:c.959A>G	ENSP00000409612.2:p.His320Arg
ENST00000481374.1:n.220A>G
ENST00000525808.5:c.*533A>G	ENSP00000434823.1:n.*533A>G
ENST00000526129.5:c.*731A>G	ENSP00000434092.1:n.*731A>G
ENST00000526196.5:c.*715A>G	ENSP00000431953.1:n.*715A>G
ENST00000528016.1:c.160-8054A>G	ENSP00000434284.1:n.160-8054A>G
ENST00000529059.5:n.856A>G
ENST00000532207.5:n.677A>G
ENST00000534334.5:c.*688A>G	ENSP00000435584.1:n.*688A>G
ENST00000541113.5:c.839A>G	ENSP00000442324.1:p.His280Arg
NM_000016.5:c.947A>G	NP_000007.1:p.His316Arg
NM_001127328.2:c.959A>G	NP_001120800.1:p.His320Arg
NM_001286042.1:c.839A>G	NP_001272971.1:p.His280Arg
NM_001286043.1:c.1046A>G	NP_001272972.1:p.His349Arg
NM_001286044.1:c.380A>G	NP_001272973.1:p.His127Arg
NM_000016.6:c.947A>G MANE Select	NP_000007.1:p.His316Arg
NM_001127328.3:c.959A>G	NP_001120800.1:p.His320Arg
NM_001286042.2:c.839A>G	NP_001272971.1:p.His280Arg
NM_001286043.2:c.1046A>G	NP_001272972.1:p.His349Arg
NM_001286044.2:c.380A>G	NP_001272973.1:p.His127Arg