Canonical Allele Identifier: CA418544855

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215172A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749487A>G , CM000663.2:g.75749487A>G	GRCh38
NC_000001.10:g.76215172A>G , CM000663.1:g.76215172A>G	GRCh37
NC_000001.9:g.75987760A>G	NCBI36
NG_007045.2:g.30130A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.777A>G MANE Select	ENSP00000359878.5:p.Lys259=
ENST00000473018.3:n.2901A>G
ENST00000532207.6:n.1666A>G
ENST00000541113.6:c.777A>G	ENSP00000442324.2:p.Lys259=
ENST00000679509.1:n.1739A>G
ENST00000679530.1:c.*545A>G	ENSP00000506454.1:n.*545A>G
ENST00000679615.1:n.2792A>G
ENST00000679687.1:c.339A>G	ENSP00000506598.1:p.Lys113=
ENST00000679704.1:c.*543A>G	ENSP00000505117.1:n.*543A>G
ENST00000679709.1:c.*740A>G	ENSP00000506623.1:n.*740A>G
ENST00000679976.1:c.*361A>G	ENSP00000505565.1:n.*361A>G
ENST00000680166.1:n.4066A>G
ENST00000680517.1:c.*165A>G	ENSP00000505803.1:n.*165A>G
ENST00000680582.1:n.1739A>G
ENST00000680613.1:c.*148A>G	ENSP00000506114.1:n.*148A>G
ENST00000680662.1:c.*691A>G	ENSP00000505080.1:n.*691A>G
ENST00000680691.1:c.*440A>G	ENSP00000506487.1:n.*440A>G
ENST00000680694.1:c.*365A>G	ENSP00000505658.1:n.*365A>G
ENST00000680743.1:c.*444A>G	ENSP00000505073.1:n.*444A>G
ENST00000680749.1:c.*62A>G	ENSP00000505122.1:n.*62A>G
ENST00000680798.1:c.*252A>G	ENSP00000505670.1:n.*252A>G
ENST00000680805.1:c.709-964A>G	ENSP00000505447.1:n.709-964A>G
ENST00000680844.1:c.*561A>G	ENSP00000506541.1:n.*561A>G
ENST00000680948.1:c.*644A>G	ENSP00000505441.1:n.*644A>G
ENST00000680964.1:c.777A>G	ENSP00000505961.1:p.Lys259=
ENST00000681037.1:c.*2261A>G	ENSP00000506025.1:n.*2261A>G
ENST00000681063.1:c.600-964A>G	ENSP00000506616.1:n.600-964A>G
ENST00000681209.1:c.*432A>G	ENSP00000505877.1:n.*432A>G
ENST00000681278.1:n.1134A>G
ENST00000681289.1:n.4772A>G
ENST00000681361.1:c.*444A>G	ENSP00000506679.1:n.*444A>G
ENST00000681430.1:c.777A>G	ENSP00000506301.1:p.Lys259=
ENST00000681446.1:c.*359A>G	ENSP00000506244.1:n.*359A>G
ENST00000681450.1:c.*448A>G	ENSP00000505660.1:n.*448A>G
ENST00000681548.1:c.*363A>G	ENSP00000505275.1:n.*363A>G
ENST00000681616.1:c.*436A>G	ENSP00000505111.1:n.*436A>G
ENST00000681621.1:c.*361A>G	ENSP00000505770.1:n.*361A>G
ENST00000681680.1:n.2872A>G
ENST00000681720.1:c.*232A>G	ENSP00000505438.1:n.*232A>G
ENST00000681730.1:n.999A>G
ENST00000681790.1:c.519A>G	ENSP00000505130.1:p.Lys173=
ENST00000681837.1:n.1393A>G
ENST00000681913.1:n.2901A>G
ENST00000681916.1:c.*545A>G	ENSP00000506477.1:n.*545A>G
ENST00000681930.1:n.2901A>G
ENST00000370834.9:c.876A>G	ENSP00000359871.5:p.Lys292=
ENST00000370841.8:c.777A>G	ENSP00000359878.4:p.Lys259=
ENST00000420607.6:c.789A>G	ENSP00000409612.2:p.Lys263=
ENST00000525808.5:c.*363A>G	ENSP00000434823.1:n.*363A>G
ENST00000526129.5:c.*561A>G	ENSP00000434092.1:n.*561A>G
ENST00000526196.5:c.*545A>G	ENSP00000431953.1:n.*545A>G
ENST00000526930.1:n.550A>G
ENST00000529059.5:n.686A>G
ENST00000530953.6:c.*274A>G	ENSP00000431372.1:n.*274A>G
ENST00000532207.5:n.507A>G
ENST00000532509.5:c.*541A>G	ENSP00000432522.1:n.*541A>G
ENST00000534334.5:c.*361A>G	ENSP00000435584.1:n.*361A>G
ENST00000541113.5:c.669A>G	ENSP00000442324.1:p.Lys223=
NM_000016.5:c.777A>G	NP_000007.1:p.Lys259=
NM_001127328.2:c.789A>G	NP_001120800.1:p.Lys263=
NM_001286042.1:c.669A>G	NP_001272971.1:p.Lys223=
NM_001286043.1:c.876A>G	NP_001272972.1:p.Lys292=
NM_001286044.1:c.210A>G	NP_001272973.1:p.Lys70=
NM_000016.6:c.777A>G MANE Select	NP_000007.1:p.Lys259=
NM_001127328.3:c.789A>G	NP_001120800.1:p.Lys263=
NM_001286042.2:c.669A>G	NP_001272971.1:p.Lys223=
NM_001286043.2:c.876A>G	NP_001272972.1:p.Lys292=
NM_001286044.2:c.210A>G	NP_001272973.1:p.Lys70=