Canonical Allele Identifier: CA418545062

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216228A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750543A>G , CM000663.2:g.75750543A>G	GRCh38
NC_000001.10:g.76216228A>G , CM000663.1:g.76216228A>G	GRCh37
NC_000001.9:g.75988816A>G	NCBI36
NG_007045.2:g.31186A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.942A>G MANE Select	ENSP00000359878.5:p.Val314=
ENST00000473018.3:n.3066A>G
ENST00000532207.6:n.1831A>G
ENST00000541113.6:c.849+984A>G	ENSP00000442324.2:n.849+984A>G
ENST00000679509.1:n.1904A>G
ENST00000679530.1:c.*710A>G	ENSP00000506454.1:n.*710A>G
ENST00000679615.1:n.2957A>G
ENST00000679687.1:c.504A>G	ENSP00000506598.1:p.Val168=
ENST00000679704.1:c.*708A>G	ENSP00000505117.1:n.*708A>G
ENST00000679709.1:c.*905A>G	ENSP00000506623.1:n.*905A>G
ENST00000679976.1:c.*526A>G	ENSP00000505565.1:n.*526A>G
ENST00000680166.1:n.4231A>G
ENST00000680315.1:n.825A>G
ENST00000680517.1:c.*330A>G	ENSP00000505803.1:n.*330A>G
ENST00000680582.1:n.1904A>G
ENST00000680613.1:c.*313A>G	ENSP00000506114.1:n.*313A>G
ENST00000680662.1:c.*856A>G	ENSP00000505080.1:n.*856A>G
ENST00000680691.1:c.*605A>G	ENSP00000506487.1:n.*605A>G
ENST00000680694.1:c.*530A>G	ENSP00000505658.1:n.*530A>G
ENST00000680743.1:c.*609A>G	ENSP00000505073.1:n.*609A>G
ENST00000680749.1:c.*227A>G	ENSP00000505122.1:n.*227A>G
ENST00000680798.1:c.*417A>G	ENSP00000505670.1:n.*417A>G
ENST00000680805.1:c.801A>G	ENSP00000505447.1:p.Val267=
ENST00000680844.1:c.*726A>G	ENSP00000506541.1:n.*726A>G
ENST00000680948.1:c.*809A>G	ENSP00000505441.1:n.*809A>G
ENST00000680964.1:c.942A>G	ENSP00000505961.1:p.Val314=
ENST00000681037.1:c.*2426A>G	ENSP00000506025.1:n.*2426A>G
ENST00000681063.1:c.*89A>G	ENSP00000506616.1:n.*89A>G
ENST00000681209.1:c.*597A>G	ENSP00000505877.1:n.*597A>G
ENST00000681278.1:n.1299A>G
ENST00000681289.1:n.4937A>G
ENST00000681361.1:c.*609A>G	ENSP00000506679.1:n.*609A>G
ENST00000681430.1:c.942A>G	ENSP00000506301.1:p.Val314=
ENST00000681446.1:c.*524A>G	ENSP00000506244.1:n.*524A>G
ENST00000681450.1:c.*613A>G	ENSP00000505660.1:n.*613A>G
ENST00000681548.1:c.*528A>G	ENSP00000505275.1:n.*528A>G
ENST00000681616.1:c.*601A>G	ENSP00000505111.1:n.*601A>G
ENST00000681621.1:c.*526A>G	ENSP00000505770.1:n.*526A>G
ENST00000681680.1:n.3037A>G
ENST00000681720.1:c.*397A>G	ENSP00000505438.1:n.*397A>G
ENST00000681730.1:n.1164A>G
ENST00000681790.1:c.684A>G	ENSP00000505130.1:p.Val228=
ENST00000681837.1:n.1558A>G
ENST00000681913.1:n.3066A>G
ENST00000681916.1:c.*710A>G	ENSP00000506477.1:n.*710A>G
ENST00000681930.1:n.3066A>G
ENST00000370834.9:c.1041A>G	ENSP00000359871.5:p.Val347=
ENST00000370841.8:c.942A>G	ENSP00000359878.4:p.Val314=
ENST00000420607.6:c.954A>G	ENSP00000409612.2:p.Val318=
ENST00000481374.1:n.93A>G
ENST00000525808.5:c.*528A>G	ENSP00000434823.1:n.*528A>G
ENST00000526129.5:c.*726A>G	ENSP00000434092.1:n.*726A>G
ENST00000526196.5:c.*710A>G	ENSP00000431953.1:n.*710A>G
ENST00000528016.1:c.156A>G	ENSP00000434284.1:p.Val52=
ENST00000529059.5:n.851A>G
ENST00000532207.5:n.672A>G
ENST00000534334.5:c.*526A>G	ENSP00000435584.1:n.*526A>G
ENST00000541113.5:c.834A>G	ENSP00000442324.1:p.Val278=
NM_000016.5:c.942A>G	NP_000007.1:p.Val314=
NM_001127328.2:c.954A>G	NP_001120800.1:p.Val318=
NM_001286042.1:c.834A>G	NP_001272971.1:p.Val278=
NM_001286043.1:c.1041A>G	NP_001272972.1:p.Val347=
NM_001286044.1:c.375A>G	NP_001272973.1:p.Val125=
NM_000016.6:c.942A>G MANE Select	NP_000007.1:p.Val314=
NM_001127328.3:c.954A>G	NP_001120800.1:p.Val318=
NM_001286042.2:c.834A>G	NP_001272971.1:p.Val278=
NM_001286043.2:c.1041A>G	NP_001272972.1:p.Val347=
NM_001286044.2:c.375A>G	NP_001272973.1:p.Val125=