Canonical Allele Identifier: CA418707759

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227001A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761316A>T , CM000663.2:g.75761316A>T	GRCh38
NC_000001.10:g.76227001A>T , CM000663.1:g.76227001A>T	GRCh37
NC_000001.9:g.75999589A>T	NCBI36
NG_007045.2:g.41959A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1140A>T MANE Select	ENSP00000359878.5:p.Gly380=
ENST00000473018.3:n.3264A>T
ENST00000532207.6:n.2151A>T
ENST00000541113.6:c.1044A>T	ENSP00000442324.2:p.Gly348=
ENST00000679509.1:n.2102A>T
ENST00000679530.1:c.*908A>T	ENSP00000506454.1:n.*908A>T
ENST00000679615.1:n.3155A>T
ENST00000679687.1:c.702A>T	ENSP00000506598.1:p.Gly234=
ENST00000679704.1:c.*906A>T	ENSP00000505117.1:n.*906A>T
ENST00000679709.1:c.*1103A>T	ENSP00000506623.1:n.*1103A>T
ENST00000679976.1:c.*724A>T	ENSP00000505565.1:n.*724A>T
ENST00000680166.1:n.4429A>T
ENST00000680315.1:n.1023A>T
ENST00000680517.1:c.*528A>T	ENSP00000505803.1:n.*528A>T
ENST00000680582.1:n.2102A>T
ENST00000680613.1:c.*633A>T	ENSP00000506114.1:n.*633A>T
ENST00000680662.1:c.*1054A>T	ENSP00000505080.1:n.*1054A>T
ENST00000680691.1:c.*803A>T	ENSP00000506487.1:n.*803A>T
ENST00000680694.1:c.*728A>T	ENSP00000505658.1:n.*728A>T
ENST00000680743.1:c.*929A>T	ENSP00000505073.1:n.*929A>T
ENST00000680749.1:c.*425A>T	ENSP00000505122.1:n.*425A>T
ENST00000680798.1:c.*615A>T	ENSP00000505670.1:n.*615A>T
ENST00000680805.1:c.999A>T	ENSP00000505447.1:p.Gly333=
ENST00000680844.1:c.*924A>T	ENSP00000506541.1:n.*924A>T
ENST00000680948.1:c.*1007A>T	ENSP00000505441.1:n.*1007A>T
ENST00000680964.1:c.*233A>T	ENSP00000505961.1:n.*233A>T
ENST00000681037.1:c.*2624A>T	ENSP00000506025.1:n.*2624A>T
ENST00000681063.1:c.*409A>T	ENSP00000506616.1:n.*409A>T
ENST00000681209.1:c.*795A>T	ENSP00000505877.1:n.*795A>T
ENST00000681278.1:n.1842A>T
ENST00000681289.1:n.5135A>T
ENST00000681361.1:c.*807A>T	ENSP00000506679.1:n.*807A>T
ENST00000681430.1:c.*233A>T	ENSP00000506301.1:n.*233A>T
ENST00000681446.1:c.*844A>T	ENSP00000506244.1:n.*844A>T
ENST00000681450.1:c.*811A>T	ENSP00000505660.1:n.*811A>T
ENST00000681548.1:c.*726A>T	ENSP00000505275.1:n.*726A>T
ENST00000681616.1:c.*799A>T	ENSP00000505111.1:n.*799A>T
ENST00000681621.1:c.*724A>T	ENSP00000505770.1:n.*724A>T
ENST00000681680.1:n.3235A>T
ENST00000681720.1:c.*595A>T	ENSP00000505438.1:n.*595A>T
ENST00000681730.1:n.1362A>T
ENST00000681790.1:c.882A>T	ENSP00000505130.1:p.Gly294=
ENST00000681837.1:n.1756A>T
ENST00000681913.1:n.3386A>T
ENST00000681916.1:c.*908A>T	ENSP00000506477.1:n.*908A>T
ENST00000681930.1:n.3264A>T
ENST00000370834.9:c.1239A>T	ENSP00000359871.5:p.Gly413=
ENST00000370841.8:c.1140A>T	ENSP00000359878.4:p.Gly380=
ENST00000420607.6:c.1152A>T	ENSP00000409612.2:p.Gly384=
ENST00000481374.1:n.413A>T
ENST00000525808.5:c.*726A>T	ENSP00000434823.1:n.*726A>T
ENST00000526129.5:c.*924A>T	ENSP00000434092.1:n.*924A>T
ENST00000526196.5:c.*908A>T	ENSP00000431953.1:n.*908A>T
ENST00000528016.1:c.160-7861A>T	ENSP00000434284.1:n.160-7861A>T
ENST00000529059.5:n.1049A>T
ENST00000541113.5:c.1032A>T	ENSP00000442324.1:p.Gly344=
NM_000016.5:c.1140A>T	NP_000007.1:p.Gly380=
NM_001127328.2:c.1152A>T	NP_001120800.1:p.Gly384=
NM_001286042.1:c.1032A>T	NP_001272971.1:p.Gly344=
NM_001286043.1:c.1239A>T	NP_001272972.1:p.Gly413=
NM_001286044.1:c.573A>T	NP_001272973.1:p.Gly191=
NM_000016.6:c.1140A>T MANE Select	NP_000007.1:p.Gly380=
NM_001127328.3:c.1152A>T	NP_001120800.1:p.Gly384=
NM_001286042.2:c.1032A>T	NP_001272971.1:p.Gly344=
NM_001286043.2:c.1239A>T	NP_001272972.1:p.Gly413=
NM_001286044.2:c.573A>T	NP_001272973.1:p.Gly191=