Canonical Allele Identifier: CA418545024

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216168A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750483A>G , CM000663.2:g.75750483A>G	GRCh38
NC_000001.10:g.76216168A>G , CM000663.1:g.76216168A>G	GRCh37
NC_000001.9:g.75988756A>G	NCBI36
NG_007045.2:g.31126A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.882A>G MANE Select	ENSP00000359878.5:p.Arg294=
ENST00000473018.3:n.3006A>G
ENST00000532207.6:n.1771A>G
ENST00000541113.6:c.849+924A>G	ENSP00000442324.2:n.849+924A>G
ENST00000679509.1:n.1844A>G
ENST00000679530.1:c.*650A>G	ENSP00000506454.1:n.*650A>G
ENST00000679615.1:n.2897A>G
ENST00000679687.1:c.444A>G	ENSP00000506598.1:p.Arg148=
ENST00000679704.1:c.*648A>G	ENSP00000505117.1:n.*648A>G
ENST00000679709.1:c.*845A>G	ENSP00000506623.1:n.*845A>G
ENST00000679976.1:c.*466A>G	ENSP00000505565.1:n.*466A>G
ENST00000680166.1:n.4171A>G
ENST00000680315.1:n.765A>G
ENST00000680517.1:c.*270A>G	ENSP00000505803.1:n.*270A>G
ENST00000680582.1:n.1844A>G
ENST00000680613.1:c.*253A>G	ENSP00000506114.1:n.*253A>G
ENST00000680662.1:c.*796A>G	ENSP00000505080.1:n.*796A>G
ENST00000680691.1:c.*545A>G	ENSP00000506487.1:n.*545A>G
ENST00000680694.1:c.*470A>G	ENSP00000505658.1:n.*470A>G
ENST00000680743.1:c.*549A>G	ENSP00000505073.1:n.*549A>G
ENST00000680749.1:c.*167A>G	ENSP00000505122.1:n.*167A>G
ENST00000680798.1:c.*357A>G	ENSP00000505670.1:n.*357A>G
ENST00000680805.1:c.741A>G	ENSP00000505447.1:p.Arg247=
ENST00000680844.1:c.*666A>G	ENSP00000506541.1:n.*666A>G
ENST00000680948.1:c.*749A>G	ENSP00000505441.1:n.*749A>G
ENST00000680964.1:c.882A>G	ENSP00000505961.1:p.Arg294=
ENST00000681037.1:c.*2366A>G	ENSP00000506025.1:n.*2366A>G
ENST00000681063.1:c.*29A>G	ENSP00000506616.1:n.*29A>G
ENST00000681209.1:c.*537A>G	ENSP00000505877.1:n.*537A>G
ENST00000681278.1:n.1239A>G
ENST00000681289.1:n.4877A>G
ENST00000681361.1:c.*549A>G	ENSP00000506679.1:n.*549A>G
ENST00000681430.1:c.882A>G	ENSP00000506301.1:p.Arg294=
ENST00000681446.1:c.*464A>G	ENSP00000506244.1:n.*464A>G
ENST00000681450.1:c.*553A>G	ENSP00000505660.1:n.*553A>G
ENST00000681548.1:c.*468A>G	ENSP00000505275.1:n.*468A>G
ENST00000681616.1:c.*541A>G	ENSP00000505111.1:n.*541A>G
ENST00000681621.1:c.*466A>G	ENSP00000505770.1:n.*466A>G
ENST00000681680.1:n.2977A>G
ENST00000681720.1:c.*337A>G	ENSP00000505438.1:n.*337A>G
ENST00000681730.1:n.1104A>G
ENST00000681790.1:c.624A>G	ENSP00000505130.1:p.Arg208=
ENST00000681837.1:n.1498A>G
ENST00000681913.1:n.3006A>G
ENST00000681916.1:c.*650A>G	ENSP00000506477.1:n.*650A>G
ENST00000681930.1:n.3006A>G
ENST00000370834.9:c.981A>G	ENSP00000359871.5:p.Arg327=
ENST00000370841.8:c.882A>G	ENSP00000359878.4:p.Arg294=
ENST00000420607.6:c.894A>G	ENSP00000409612.2:p.Arg298=
ENST00000481374.1:n.33A>G
ENST00000525808.5:c.*468A>G	ENSP00000434823.1:n.*468A>G
ENST00000526129.5:c.*666A>G	ENSP00000434092.1:n.*666A>G
ENST00000526196.5:c.*650A>G	ENSP00000431953.1:n.*650A>G
ENST00000528016.1:c.96A>G	ENSP00000434284.1:p.Arg32=
ENST00000529059.5:n.791A>G
ENST00000532207.5:n.612A>G
ENST00000534334.5:c.*466A>G	ENSP00000435584.1:n.*466A>G
ENST00000541113.5:c.774A>G	ENSP00000442324.1:p.Arg258=
NM_000016.5:c.882A>G	NP_000007.1:p.Arg294=
NM_001127328.2:c.894A>G	NP_001120800.1:p.Arg298=
NM_001286042.1:c.774A>G	NP_001272971.1:p.Arg258=
NM_001286043.1:c.981A>G	NP_001272972.1:p.Arg327=
NM_001286044.1:c.315A>G	NP_001272973.1:p.Arg105=
NM_000016.6:c.882A>G MANE Select	NP_000007.1:p.Arg294=
NM_001127328.3:c.894A>G	NP_001120800.1:p.Arg298=
NM_001286042.2:c.774A>G	NP_001272971.1:p.Arg258=
NM_001286043.2:c.981A>G	NP_001272972.1:p.Arg327=
NM_001286044.2:c.315A>G	NP_001272973.1:p.Arg105=