Canonical Allele Identifier: CA418544786

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215124A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749439A>T , CM000663.2:g.75749439A>T	GRCh38
NC_000001.10:g.76215124A>T , CM000663.1:g.76215124A>T	GRCh37
NC_000001.9:g.75987712A>T	NCBI36
NG_007045.2:g.30082A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.729A>T MANE Select	ENSP00000359878.5:p.Arg243=
ENST00000473018.3:n.2853A>T
ENST00000532207.6:n.1618A>T
ENST00000541113.6:c.729A>T	ENSP00000442324.2:p.Arg243=
ENST00000679509.1:n.1691A>T
ENST00000679530.1:c.*497A>T	ENSP00000506454.1:n.*497A>T
ENST00000679615.1:n.2744A>T
ENST00000679687.1:c.291A>T	ENSP00000506598.1:p.Arg97=
ENST00000679704.1:c.*495A>T	ENSP00000505117.1:n.*495A>T
ENST00000679709.1:c.*692A>T	ENSP00000506623.1:n.*692A>T
ENST00000679976.1:c.*313A>T	ENSP00000505565.1:n.*313A>T
ENST00000680166.1:n.4018A>T
ENST00000680517.1:c.*117A>T	ENSP00000505803.1:n.*117A>T
ENST00000680582.1:n.1691A>T
ENST00000680613.1:c.*100A>T	ENSP00000506114.1:n.*100A>T
ENST00000680662.1:c.*643A>T	ENSP00000505080.1:n.*643A>T
ENST00000680691.1:c.*392A>T	ENSP00000506487.1:n.*392A>T
ENST00000680694.1:c.*317A>T	ENSP00000505658.1:n.*317A>T
ENST00000680743.1:c.*396A>T	ENSP00000505073.1:n.*396A>T
ENST00000680749.1:c.*14A>T	ENSP00000505122.1:n.*14A>T
ENST00000680798.1:c.*204A>T	ENSP00000505670.1:n.*204A>T
ENST00000680805.1:c.709-1012A>T	ENSP00000505447.1:n.709-1012A>T
ENST00000680844.1:c.*513A>T	ENSP00000506541.1:n.*513A>T
ENST00000680948.1:c.*596A>T	ENSP00000505441.1:n.*596A>T
ENST00000680964.1:c.729A>T	ENSP00000505961.1:p.Arg243=
ENST00000681037.1:c.*2213A>T	ENSP00000506025.1:n.*2213A>T
ENST00000681063.1:c.600-1012A>T	ENSP00000506616.1:n.600-1012A>T
ENST00000681209.1:c.*384A>T	ENSP00000505877.1:n.*384A>T
ENST00000681278.1:n.1086A>T
ENST00000681289.1:n.4724A>T
ENST00000681361.1:c.*396A>T	ENSP00000506679.1:n.*396A>T
ENST00000681430.1:c.729A>T	ENSP00000506301.1:p.Arg243=
ENST00000681446.1:c.*311A>T	ENSP00000506244.1:n.*311A>T
ENST00000681450.1:c.*400A>T	ENSP00000505660.1:n.*400A>T
ENST00000681548.1:c.*315A>T	ENSP00000505275.1:n.*315A>T
ENST00000681616.1:c.*388A>T	ENSP00000505111.1:n.*388A>T
ENST00000681621.1:c.*313A>T	ENSP00000505770.1:n.*313A>T
ENST00000681680.1:n.2824A>T
ENST00000681720.1:c.*184A>T	ENSP00000505438.1:n.*184A>T
ENST00000681730.1:n.951A>T
ENST00000681790.1:c.471A>T	ENSP00000505130.1:p.Arg157=
ENST00000681837.1:n.1345A>T
ENST00000681913.1:n.2853A>T
ENST00000681916.1:c.*497A>T	ENSP00000506477.1:n.*497A>T
ENST00000681930.1:n.2853A>T
ENST00000370834.9:c.828A>T	ENSP00000359871.5:p.Arg276=
ENST00000370841.8:c.729A>T	ENSP00000359878.4:p.Arg243=
ENST00000420607.6:c.741A>T	ENSP00000409612.2:p.Arg247=
ENST00000525808.5:c.*315A>T	ENSP00000434823.1:n.*315A>T
ENST00000526129.5:c.*513A>T	ENSP00000434092.1:n.*513A>T
ENST00000526196.5:c.*497A>T	ENSP00000431953.1:n.*497A>T
ENST00000526930.1:n.502A>T
ENST00000529059.5:n.638A>T
ENST00000530953.6:c.*226A>T	ENSP00000431372.1:n.*226A>T
ENST00000532207.5:n.459A>T
ENST00000532509.5:c.*493A>T	ENSP00000432522.1:n.*493A>T
ENST00000534334.5:c.*313A>T	ENSP00000435584.1:n.*313A>T
ENST00000541113.5:c.621A>T	ENSP00000442324.1:p.Arg207=
NM_000016.5:c.729A>T	NP_000007.1:p.Arg243=
NM_001127328.2:c.741A>T	NP_001120800.1:p.Arg247=
NM_001286042.1:c.621A>T	NP_001272971.1:p.Arg207=
NM_001286043.1:c.828A>T	NP_001272972.1:p.Arg276=
NM_001286044.1:c.162A>T	NP_001272973.1:p.Arg54=
NM_000016.6:c.729A>T MANE Select	NP_000007.1:p.Arg243=
NM_001127328.3:c.741A>T	NP_001120800.1:p.Arg247=
NM_001286042.2:c.621A>T	NP_001272971.1:p.Arg207=
NM_001286043.2:c.828A>T	NP_001272972.1:p.Arg276=
NM_001286044.2:c.162A>T	NP_001272973.1:p.Arg54=