Canonical Allele Identifier: CA418707549

Gene: ACADM

Linked Data

• dbSNP Id: rs1648830289
• MyVariant Identifiers: chr1:g.76226881A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761196A>G , CM000663.2:g.75761196A>G	GRCh38
NC_000001.10:g.76226881A>G , CM000663.1:g.76226881A>G	GRCh37
NC_000001.9:g.75999469A>G	NCBI36
NG_007045.2:g.41839A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1020A>G MANE Select	ENSP00000359878.5:p.Ala340=
ENST00000473018.3:n.3144A>G
ENST00000532207.6:n.2031A>G
ENST00000541113.6:c.924A>G	ENSP00000442324.2:p.Ala308=
ENST00000679509.1:n.1982A>G
ENST00000679530.1:c.*788A>G	ENSP00000506454.1:n.*788A>G
ENST00000679615.1:n.3035A>G
ENST00000679687.1:c.582A>G	ENSP00000506598.1:p.Ala194=
ENST00000679704.1:c.*786A>G	ENSP00000505117.1:n.*786A>G
ENST00000679709.1:c.*983A>G	ENSP00000506623.1:n.*983A>G
ENST00000679976.1:c.*604A>G	ENSP00000505565.1:n.*604A>G
ENST00000680166.1:n.4309A>G
ENST00000680315.1:n.903A>G
ENST00000680517.1:c.*408A>G	ENSP00000505803.1:n.*408A>G
ENST00000680582.1:n.1982A>G
ENST00000680613.1:c.*513A>G	ENSP00000506114.1:n.*513A>G
ENST00000680662.1:c.*934A>G	ENSP00000505080.1:n.*934A>G
ENST00000680691.1:c.*683A>G	ENSP00000506487.1:n.*683A>G
ENST00000680694.1:c.*608A>G	ENSP00000505658.1:n.*608A>G
ENST00000680743.1:c.*809A>G	ENSP00000505073.1:n.*809A>G
ENST00000680749.1:c.*305A>G	ENSP00000505122.1:n.*305A>G
ENST00000680798.1:c.*495A>G	ENSP00000505670.1:n.*495A>G
ENST00000680805.1:c.879A>G	ENSP00000505447.1:p.Ala293=
ENST00000680844.1:c.*804A>G	ENSP00000506541.1:n.*804A>G
ENST00000680948.1:c.*887A>G	ENSP00000505441.1:n.*887A>G
ENST00000680964.1:c.*113A>G	ENSP00000505961.1:n.*113A>G
ENST00000681037.1:c.*2504A>G	ENSP00000506025.1:n.*2504A>G
ENST00000681063.1:c.*289A>G	ENSP00000506616.1:n.*289A>G
ENST00000681209.1:c.*675A>G	ENSP00000505877.1:n.*675A>G
ENST00000681278.1:n.1722A>G
ENST00000681289.1:n.5015A>G
ENST00000681361.1:c.*687A>G	ENSP00000506679.1:n.*687A>G
ENST00000681430.1:c.*113A>G	ENSP00000506301.1:n.*113A>G
ENST00000681446.1:c.*724A>G	ENSP00000506244.1:n.*724A>G
ENST00000681450.1:c.*691A>G	ENSP00000505660.1:n.*691A>G
ENST00000681548.1:c.*606A>G	ENSP00000505275.1:n.*606A>G
ENST00000681616.1:c.*679A>G	ENSP00000505111.1:n.*679A>G
ENST00000681621.1:c.*604A>G	ENSP00000505770.1:n.*604A>G
ENST00000681680.1:n.3115A>G
ENST00000681720.1:c.*475A>G	ENSP00000505438.1:n.*475A>G
ENST00000681730.1:n.1242A>G
ENST00000681790.1:c.762A>G	ENSP00000505130.1:p.Ala254=
ENST00000681837.1:n.1636A>G
ENST00000681913.1:n.3266A>G
ENST00000681916.1:c.*788A>G	ENSP00000506477.1:n.*788A>G
ENST00000681930.1:n.3144A>G
ENST00000370834.9:c.1119A>G	ENSP00000359871.5:p.Ala373=
ENST00000370841.8:c.1020A>G	ENSP00000359878.4:p.Ala340=
ENST00000420607.6:c.1032A>G	ENSP00000409612.2:p.Ala344=
ENST00000481374.1:n.293A>G
ENST00000525808.5:c.*606A>G	ENSP00000434823.1:n.*606A>G
ENST00000526129.5:c.*804A>G	ENSP00000434092.1:n.*804A>G
ENST00000526196.5:c.*788A>G	ENSP00000431953.1:n.*788A>G
ENST00000528016.1:c.160-7981A>G	ENSP00000434284.1:n.160-7981A>G
ENST00000529059.5:n.929A>G
ENST00000532207.5:n.750A>G
ENST00000534334.5:c.*761A>G	ENSP00000435584.1:n.*761A>G
ENST00000541113.5:c.912A>G	ENSP00000442324.1:p.Ala304=
NM_000016.5:c.1020A>G	NP_000007.1:p.Ala340=
NM_001127328.2:c.1032A>G	NP_001120800.1:p.Ala344=
NM_001286042.1:c.912A>G	NP_001272971.1:p.Ala304=
NM_001286043.1:c.1119A>G	NP_001272972.1:p.Ala373=
NM_001286044.1:c.453A>G	NP_001272973.1:p.Ala151=
NM_000016.6:c.1020A>G MANE Select	NP_000007.1:p.Ala340=
NM_001127328.3:c.1032A>G	NP_001120800.1:p.Ala344=
NM_001286042.2:c.912A>G	NP_001272971.1:p.Ala304=
NM_001286043.2:c.1119A>G	NP_001272972.1:p.Ala373=
NM_001286044.2:c.453A>G	NP_001272973.1:p.Ala151=