Canonical Allele Identifier: CA418539987

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205787A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740102A>G , CM000663.2:g.75740102A>G	GRCh38
NC_000001.10:g.76205787A>G , CM000663.1:g.76205787A>G	GRCh37
NC_000001.9:g.75978375A>G	NCBI36
NG_007045.2:g.20745A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.591A>G MANE Select	ENSP00000359878.5:p.Lys197=
ENST00000473018.3:n.2715A>G
ENST00000541113.6:c.591A>G	ENSP00000442324.2:p.Lys197=
ENST00000679509.1:n.1553A>G
ENST00000679530.1:c.*359A>G	ENSP00000506454.1:n.*359A>G
ENST00000679615.1:n.2715A>G
ENST00000679687.1:c.153A>G	ENSP00000506598.1:p.Lys51=
ENST00000679704.1:c.*357A>G	ENSP00000505117.1:n.*357A>G
ENST00000679709.1:c.*554A>G	ENSP00000506623.1:n.*554A>G
ENST00000679804.1:n.330A>G
ENST00000679976.1:c.*175A>G	ENSP00000505565.1:n.*175A>G
ENST00000680166.1:n.3880A>G
ENST00000680517.1:c.*88A>G	ENSP00000505803.1:n.*88A>G
ENST00000680582.1:n.1553A>G
ENST00000680613.1:c.591A>G	ENSP00000506114.1:p.Lys197=
ENST00000680662.1:c.*505A>G	ENSP00000505080.1:n.*505A>G
ENST00000680691.1:c.*254A>G	ENSP00000506487.1:n.*254A>G
ENST00000680694.1:c.*179A>G	ENSP00000505658.1:n.*179A>G
ENST00000680743.1:c.*258A>G	ENSP00000505073.1:n.*258A>G
ENST00000680749.1:c.591A>G	ENSP00000505122.1:p.Lys197=
ENST00000680798.1:c.*175A>G	ENSP00000505670.1:n.*175A>G
ENST00000680805.1:c.591A>G	ENSP00000505447.1:p.Lys197=
ENST00000680844.1:c.*375A>G	ENSP00000506541.1:n.*375A>G
ENST00000680948.1:c.*458A>G	ENSP00000505441.1:n.*458A>G
ENST00000680964.1:c.591A>G	ENSP00000505961.1:p.Lys197=
ENST00000681037.1:c.591A>G	ENSP00000506025.1:p.Lys197=
ENST00000681063.1:c.591A>G	ENSP00000506616.1:p.Lys197=
ENST00000681209.1:c.*355A>G	ENSP00000505877.1:n.*355A>G
ENST00000681278.1:n.948A>G
ENST00000681289.1:n.948A>G
ENST00000681361.1:c.*258A>G	ENSP00000506679.1:n.*258A>G
ENST00000681430.1:c.591A>G	ENSP00000506301.1:p.Lys197=
ENST00000681446.1:c.*173A>G	ENSP00000506244.1:n.*173A>G
ENST00000681450.1:c.*262A>G	ENSP00000505660.1:n.*262A>G
ENST00000681548.1:c.*177A>G	ENSP00000505275.1:n.*177A>G
ENST00000681616.1:c.*359A>G	ENSP00000505111.1:n.*359A>G
ENST00000681621.1:c.*175A>G	ENSP00000505770.1:n.*175A>G
ENST00000681680.1:n.2715A>G
ENST00000681720.1:c.*55-5704A>G	ENSP00000505438.1:n.*55-5704A>G
ENST00000681730.1:n.813A>G
ENST00000681790.1:c.333A>G	ENSP00000505130.1:p.Lys111=
ENST00000681837.1:n.1207A>G
ENST00000681913.1:n.2715A>G
ENST00000681916.1:c.*359A>G	ENSP00000506477.1:n.*359A>G
ENST00000681930.1:n.2715A>G
ENST00000370834.9:c.690A>G	ENSP00000359871.5:p.Lys230=
ENST00000370841.8:c.591A>G	ENSP00000359878.4:p.Lys197=
ENST00000420607.6:c.603A>G	ENSP00000409612.2:p.Lys201=
ENST00000525808.5:c.*177A>G	ENSP00000434823.1:n.*177A>G
ENST00000526129.5:c.*375A>G	ENSP00000434092.1:n.*375A>G
ENST00000526196.5:c.*359A>G	ENSP00000431953.1:n.*359A>G
ENST00000526930.1:n.364A>G
ENST00000529059.5:n.500A>G
ENST00000530953.6:c.*88A>G	ENSP00000431372.1:n.*88A>G
ENST00000532509.5:c.*355A>G	ENSP00000432522.1:n.*355A>G
ENST00000534334.5:c.*175A>G	ENSP00000435584.1:n.*175A>G
ENST00000541113.5:c.483A>G	ENSP00000442324.1:p.Lys161=
NM_000016.5:c.591A>G	NP_000007.1:p.Lys197=
NM_001127328.2:c.603A>G	NP_001120800.1:p.Lys201=
NM_001286042.1:c.483A>G	NP_001272971.1:p.Lys161=
NM_001286043.1:c.690A>G	NP_001272972.1:p.Lys230=
NM_001286044.1:c.24A>G	NP_001272973.1:p.Lys8=
NM_000016.6:c.591A>G MANE Select	NP_000007.1:p.Lys197=
NM_001127328.3:c.603A>G	NP_001120800.1:p.Lys201=
NM_001286042.2:c.483A>G	NP_001272971.1:p.Lys161=
NM_001286043.2:c.690A>G	NP_001272972.1:p.Lys230=
NM_001286044.2:c.24A>G	NP_001272973.1:p.Lys8=