Canonical Allele Identifier: CA418707594

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226908A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761223A>C , CM000663.2:g.75761223A>C	GRCh38
NC_000001.10:g.76226908A>C , CM000663.1:g.76226908A>C	GRCh37
NC_000001.9:g.75999496A>C	NCBI36
NG_007045.2:g.41866A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1047A>C MANE Select	ENSP00000359878.5:p.Arg349=
ENST00000473018.3:n.3171A>C
ENST00000532207.6:n.2058A>C
ENST00000541113.6:c.951A>C	ENSP00000442324.2:p.Arg317=
ENST00000679509.1:n.2009A>C
ENST00000679530.1:c.*815A>C	ENSP00000506454.1:n.*815A>C
ENST00000679615.1:n.3062A>C
ENST00000679687.1:c.609A>C	ENSP00000506598.1:p.Arg203=
ENST00000679704.1:c.*813A>C	ENSP00000505117.1:n.*813A>C
ENST00000679709.1:c.*1010A>C	ENSP00000506623.1:n.*1010A>C
ENST00000679976.1:c.*631A>C	ENSP00000505565.1:n.*631A>C
ENST00000680166.1:n.4336A>C
ENST00000680315.1:n.930A>C
ENST00000680517.1:c.*435A>C	ENSP00000505803.1:n.*435A>C
ENST00000680582.1:n.2009A>C
ENST00000680613.1:c.*540A>C	ENSP00000506114.1:n.*540A>C
ENST00000680662.1:c.*961A>C	ENSP00000505080.1:n.*961A>C
ENST00000680691.1:c.*710A>C	ENSP00000506487.1:n.*710A>C
ENST00000680694.1:c.*635A>C	ENSP00000505658.1:n.*635A>C
ENST00000680743.1:c.*836A>C	ENSP00000505073.1:n.*836A>C
ENST00000680749.1:c.*332A>C	ENSP00000505122.1:n.*332A>C
ENST00000680798.1:c.*522A>C	ENSP00000505670.1:n.*522A>C
ENST00000680805.1:c.906A>C	ENSP00000505447.1:p.Arg302=
ENST00000680844.1:c.*831A>C	ENSP00000506541.1:n.*831A>C
ENST00000680948.1:c.*914A>C	ENSP00000505441.1:n.*914A>C
ENST00000680964.1:c.*140A>C	ENSP00000505961.1:n.*140A>C
ENST00000681037.1:c.*2531A>C	ENSP00000506025.1:n.*2531A>C
ENST00000681063.1:c.*316A>C	ENSP00000506616.1:n.*316A>C
ENST00000681209.1:c.*702A>C	ENSP00000505877.1:n.*702A>C
ENST00000681278.1:n.1749A>C
ENST00000681289.1:n.5042A>C
ENST00000681361.1:c.*714A>C	ENSP00000506679.1:n.*714A>C
ENST00000681430.1:c.*140A>C	ENSP00000506301.1:n.*140A>C
ENST00000681446.1:c.*751A>C	ENSP00000506244.1:n.*751A>C
ENST00000681450.1:c.*718A>C	ENSP00000505660.1:n.*718A>C
ENST00000681548.1:c.*633A>C	ENSP00000505275.1:n.*633A>C
ENST00000681616.1:c.*706A>C	ENSP00000505111.1:n.*706A>C
ENST00000681621.1:c.*631A>C	ENSP00000505770.1:n.*631A>C
ENST00000681680.1:n.3142A>C
ENST00000681720.1:c.*502A>C	ENSP00000505438.1:n.*502A>C
ENST00000681730.1:n.1269A>C
ENST00000681790.1:c.789A>C	ENSP00000505130.1:p.Arg263=
ENST00000681837.1:n.1663A>C
ENST00000681913.1:n.3293A>C
ENST00000681916.1:c.*815A>C	ENSP00000506477.1:n.*815A>C
ENST00000681930.1:n.3171A>C
ENST00000370834.9:c.1146A>C	ENSP00000359871.5:p.Arg382=
ENST00000370841.8:c.1047A>C	ENSP00000359878.4:p.Arg349=
ENST00000420607.6:c.1059A>C	ENSP00000409612.2:p.Arg353=
ENST00000481374.1:n.320A>C
ENST00000525808.5:c.*633A>C	ENSP00000434823.1:n.*633A>C
ENST00000526129.5:c.*831A>C	ENSP00000434092.1:n.*831A>C
ENST00000526196.5:c.*815A>C	ENSP00000431953.1:n.*815A>C
ENST00000528016.1:c.160-7954A>C	ENSP00000434284.1:n.160-7954A>C
ENST00000529059.5:n.956A>C
ENST00000534334.5:c.*788A>C	ENSP00000435584.1:n.*788A>C
ENST00000541113.5:c.939A>C	ENSP00000442324.1:p.Arg313=
NM_000016.5:c.1047A>C	NP_000007.1:p.Arg349=
NM_001127328.2:c.1059A>C	NP_001120800.1:p.Arg353=
NM_001286042.1:c.939A>C	NP_001272971.1:p.Arg313=
NM_001286043.1:c.1146A>C	NP_001272972.1:p.Arg382=
NM_001286044.1:c.480A>C	NP_001272973.1:p.Arg160=
NM_000016.6:c.1047A>C MANE Select	NP_000007.1:p.Arg349=
NM_001127328.3:c.1059A>C	NP_001120800.1:p.Arg353=
NM_001286042.2:c.939A>C	NP_001272971.1:p.Arg313=
NM_001286043.2:c.1146A>C	NP_001272972.1:p.Arg382=
NM_001286044.2:c.480A>C	NP_001272973.1:p.Arg160=