Canonical Allele Identifier: CA418544862

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215181T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749496T>A , CM000663.2:g.75749496T>A	GRCh38
NC_000001.10:g.76215181T>A , CM000663.1:g.76215181T>A	GRCh37
NC_000001.9:g.75987769T>A	NCBI36
NG_007045.2:g.30139T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.786T>A MANE Select	ENSP00000359878.5:p.Val262=
ENST00000473018.3:n.2910T>A
ENST00000532207.6:n.1675T>A
ENST00000541113.6:c.786T>A	ENSP00000442324.2:p.Val262=
ENST00000679509.1:n.1748T>A
ENST00000679530.1:c.*554T>A	ENSP00000506454.1:n.*554T>A
ENST00000679615.1:n.2801T>A
ENST00000679687.1:c.348T>A	ENSP00000506598.1:p.Val116=
ENST00000679704.1:c.*552T>A	ENSP00000505117.1:n.*552T>A
ENST00000679709.1:c.*749T>A	ENSP00000506623.1:n.*749T>A
ENST00000679976.1:c.*370T>A	ENSP00000505565.1:n.*370T>A
ENST00000680166.1:n.4075T>A
ENST00000680517.1:c.*174T>A	ENSP00000505803.1:n.*174T>A
ENST00000680582.1:n.1748T>A
ENST00000680613.1:c.*157T>A	ENSP00000506114.1:n.*157T>A
ENST00000680662.1:c.*700T>A	ENSP00000505080.1:n.*700T>A
ENST00000680691.1:c.*449T>A	ENSP00000506487.1:n.*449T>A
ENST00000680694.1:c.*374T>A	ENSP00000505658.1:n.*374T>A
ENST00000680743.1:c.*453T>A	ENSP00000505073.1:n.*453T>A
ENST00000680749.1:c.*71T>A	ENSP00000505122.1:n.*71T>A
ENST00000680798.1:c.*261T>A	ENSP00000505670.1:n.*261T>A
ENST00000680805.1:c.709-955T>A	ENSP00000505447.1:n.709-955T>A
ENST00000680844.1:c.*570T>A	ENSP00000506541.1:n.*570T>A
ENST00000680948.1:c.*653T>A	ENSP00000505441.1:n.*653T>A
ENST00000680964.1:c.786T>A	ENSP00000505961.1:p.Val262=
ENST00000681037.1:c.*2270T>A	ENSP00000506025.1:n.*2270T>A
ENST00000681063.1:c.600-955T>A	ENSP00000506616.1:n.600-955T>A
ENST00000681209.1:c.*441T>A	ENSP00000505877.1:n.*441T>A
ENST00000681278.1:n.1143T>A
ENST00000681289.1:n.4781T>A
ENST00000681361.1:c.*453T>A	ENSP00000506679.1:n.*453T>A
ENST00000681430.1:c.786T>A	ENSP00000506301.1:p.Val262=
ENST00000681446.1:c.*368T>A	ENSP00000506244.1:n.*368T>A
ENST00000681450.1:c.*457T>A	ENSP00000505660.1:n.*457T>A
ENST00000681548.1:c.*372T>A	ENSP00000505275.1:n.*372T>A
ENST00000681616.1:c.*445T>A	ENSP00000505111.1:n.*445T>A
ENST00000681621.1:c.*370T>A	ENSP00000505770.1:n.*370T>A
ENST00000681680.1:n.2881T>A
ENST00000681720.1:c.*241T>A	ENSP00000505438.1:n.*241T>A
ENST00000681730.1:n.1008T>A
ENST00000681790.1:c.528T>A	ENSP00000505130.1:p.Val176=
ENST00000681837.1:n.1402T>A
ENST00000681913.1:n.2910T>A
ENST00000681916.1:c.*554T>A	ENSP00000506477.1:n.*554T>A
ENST00000681930.1:n.2910T>A
ENST00000370834.9:c.885T>A	ENSP00000359871.5:p.Val295=
ENST00000370841.8:c.786T>A	ENSP00000359878.4:p.Val262=
ENST00000420607.6:c.798T>A	ENSP00000409612.2:p.Val266=
ENST00000525808.5:c.*372T>A	ENSP00000434823.1:n.*372T>A
ENST00000526129.5:c.*570T>A	ENSP00000434092.1:n.*570T>A
ENST00000526196.5:c.*554T>A	ENSP00000431953.1:n.*554T>A
ENST00000526930.1:n.559T>A
ENST00000529059.5:n.695T>A
ENST00000530953.6:c.*283T>A	ENSP00000431372.1:n.*283T>A
ENST00000532207.5:n.516T>A
ENST00000532509.5:c.*550T>A	ENSP00000432522.1:n.*550T>A
ENST00000534334.5:c.*370T>A	ENSP00000435584.1:n.*370T>A
ENST00000541113.5:c.678T>A	ENSP00000442324.1:p.Val226=
NM_000016.5:c.786T>A	NP_000007.1:p.Val262=
NM_001127328.2:c.798T>A	NP_001120800.1:p.Val266=
NM_001286042.1:c.678T>A	NP_001272971.1:p.Val226=
NM_001286043.1:c.885T>A	NP_001272972.1:p.Val295=
NM_001286044.1:c.219T>A	NP_001272973.1:p.Val73=
NM_000016.6:c.786T>A MANE Select	NP_000007.1:p.Val262=
NM_001127328.3:c.798T>A	NP_001120800.1:p.Val266=
NM_001286042.2:c.678T>A	NP_001272971.1:p.Val226=
NM_001286043.2:c.885T>A	NP_001272972.1:p.Val295=
NM_001286044.2:c.219T>A	NP_001272973.1:p.Val73=