Canonical Allele Identifier: CA418545007

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216150T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750465T>G , CM000663.2:g.75750465T>G	GRCh38
NC_000001.10:g.76216150T>G , CM000663.1:g.76216150T>G	GRCh37
NC_000001.9:g.75988738T>G	NCBI36
NG_007045.2:g.31108T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.864T>G MANE Select	ENSP00000359878.5:p.Ala288=
ENST00000473018.3:n.2988T>G
ENST00000532207.6:n.1753T>G
ENST00000541113.6:c.849+906T>G	ENSP00000442324.2:n.849+906T>G
ENST00000679509.1:n.1826T>G
ENST00000679530.1:c.*632T>G	ENSP00000506454.1:n.*632T>G
ENST00000679615.1:n.2879T>G
ENST00000679687.1:c.426T>G	ENSP00000506598.1:p.Ala142=
ENST00000679704.1:c.*630T>G	ENSP00000505117.1:n.*630T>G
ENST00000679709.1:c.*827T>G	ENSP00000506623.1:n.*827T>G
ENST00000679976.1:c.*448T>G	ENSP00000505565.1:n.*448T>G
ENST00000680166.1:n.4153T>G
ENST00000680315.1:n.747T>G
ENST00000680517.1:c.*252T>G	ENSP00000505803.1:n.*252T>G
ENST00000680582.1:n.1826T>G
ENST00000680613.1:c.*235T>G	ENSP00000506114.1:n.*235T>G
ENST00000680662.1:c.*778T>G	ENSP00000505080.1:n.*778T>G
ENST00000680691.1:c.*527T>G	ENSP00000506487.1:n.*527T>G
ENST00000680694.1:c.*452T>G	ENSP00000505658.1:n.*452T>G
ENST00000680743.1:c.*531T>G	ENSP00000505073.1:n.*531T>G
ENST00000680749.1:c.*149T>G	ENSP00000505122.1:n.*149T>G
ENST00000680798.1:c.*339T>G	ENSP00000505670.1:n.*339T>G
ENST00000680805.1:c.723T>G	ENSP00000505447.1:p.Ala241=
ENST00000680844.1:c.*648T>G	ENSP00000506541.1:n.*648T>G
ENST00000680948.1:c.*731T>G	ENSP00000505441.1:n.*731T>G
ENST00000680964.1:c.864T>G	ENSP00000505961.1:p.Ala288=
ENST00000681037.1:c.*2348T>G	ENSP00000506025.1:n.*2348T>G
ENST00000681063.1:c.*11T>G	ENSP00000506616.1:n.*11T>G
ENST00000681209.1:c.*519T>G	ENSP00000505877.1:n.*519T>G
ENST00000681278.1:n.1221T>G
ENST00000681289.1:n.4859T>G
ENST00000681361.1:c.*531T>G	ENSP00000506679.1:n.*531T>G
ENST00000681430.1:c.864T>G	ENSP00000506301.1:p.Ala288=
ENST00000681446.1:c.*446T>G	ENSP00000506244.1:n.*446T>G
ENST00000681450.1:c.*535T>G	ENSP00000505660.1:n.*535T>G
ENST00000681548.1:c.*450T>G	ENSP00000505275.1:n.*450T>G
ENST00000681616.1:c.*523T>G	ENSP00000505111.1:n.*523T>G
ENST00000681621.1:c.*448T>G	ENSP00000505770.1:n.*448T>G
ENST00000681680.1:n.2959T>G
ENST00000681720.1:c.*319T>G	ENSP00000505438.1:n.*319T>G
ENST00000681730.1:n.1086T>G
ENST00000681790.1:c.606T>G	ENSP00000505130.1:p.Ala202=
ENST00000681837.1:n.1480T>G
ENST00000681913.1:n.2988T>G
ENST00000681916.1:c.*632T>G	ENSP00000506477.1:n.*632T>G
ENST00000681930.1:n.2988T>G
ENST00000370834.9:c.963T>G	ENSP00000359871.5:p.Ala321=
ENST00000370841.8:c.864T>G	ENSP00000359878.4:p.Ala288=
ENST00000420607.6:c.876T>G	ENSP00000409612.2:p.Ala292=
ENST00000481374.1:n.15T>G
ENST00000525808.5:c.*450T>G	ENSP00000434823.1:n.*450T>G
ENST00000526129.5:c.*648T>G	ENSP00000434092.1:n.*648T>G
ENST00000526196.5:c.*632T>G	ENSP00000431953.1:n.*632T>G
ENST00000528016.1:c.78T>G	ENSP00000434284.1:p.Ala26=
ENST00000529059.5:n.773T>G
ENST00000532207.5:n.594T>G
ENST00000534334.5:c.*448T>G	ENSP00000435584.1:n.*448T>G
ENST00000541113.5:c.756T>G	ENSP00000442324.1:p.Ala252=
NM_000016.5:c.864T>G	NP_000007.1:p.Ala288=
NM_001127328.2:c.876T>G	NP_001120800.1:p.Ala292=
NM_001286042.1:c.756T>G	NP_001272971.1:p.Ala252=
NM_001286043.1:c.963T>G	NP_001272972.1:p.Ala321=
NM_001286044.1:c.297T>G	NP_001272973.1:p.Ala99=
NM_000016.6:c.864T>G MANE Select	NP_000007.1:p.Ala288=
NM_001127328.3:c.876T>G	NP_001120800.1:p.Ala292=
NM_001286042.2:c.756T>G	NP_001272971.1:p.Ala252=
NM_001286043.2:c.963T>G	NP_001272972.1:p.Ala321=
NM_001286044.2:c.297T>G	NP_001272973.1:p.Ala99=