Canonical Allele Identifier: CA418539895
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76205694C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740009C>A , CM000663.2:g.75740009C>A GRCh38
NC_000001.10:g.76205694C>A , CM000663.1:g.76205694C>A GRCh37
NC_000001.9:g.75978282C>A NCBI36
NG_007045.2:g.20652C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.498C>A MANE Select ENSP00000359878.5:p.Gly166=
ENST00000473018.3:n.2622C>A
ENST00000541113.6:c.498C>A ENSP00000442324.2:p.Gly166=
ENST00000679509.1:n.1460C>A
ENST00000679530.1:c.*266C>A ENSP00000506454.1:n.*266C>A
ENST00000679615.1:n.2622C>A
ENST00000679687.1:c.60C>A ENSP00000506598.1:p.Gly20=
ENST00000679704.1:c.*264C>A ENSP00000505117.1:n.*264C>A
ENST00000679709.1:c.*461C>A ENSP00000506623.1:n.*461C>A
ENST00000679804.1:n.237C>A
ENST00000679976.1:c.*82C>A ENSP00000505565.1:n.*82C>A
ENST00000680166.1:n.3787C>A
ENST00000680517.1:c.316C>A ENSP00000505803.1:p.Leu106Ile
ENST00000680582.1:n.1460C>A
ENST00000680613.1:c.498C>A ENSP00000506114.1:p.Gly166=
ENST00000680662.1:c.*412C>A ENSP00000505080.1:n.*412C>A
ENST00000680691.1:c.*161C>A ENSP00000506487.1:n.*161C>A
ENST00000680694.1:c.*86C>A ENSP00000505658.1:n.*86C>A
ENST00000680743.1:c.*165C>A ENSP00000505073.1:n.*165C>A
ENST00000680749.1:c.498C>A ENSP00000505122.1:p.Gly166=
ENST00000680798.1:c.*82C>A ENSP00000505670.1:n.*82C>A
ENST00000680805.1:c.498C>A ENSP00000505447.1:p.Gly166=
ENST00000680844.1:c.*282C>A ENSP00000506541.1:n.*282C>A
ENST00000680948.1:c.*365C>A ENSP00000505441.1:n.*365C>A
ENST00000680964.1:c.498C>A ENSP00000505961.1:p.Gly166=
ENST00000681037.1:c.498C>A ENSP00000506025.1:p.Gly166=
ENST00000681063.1:c.498C>A ENSP00000506616.1:p.Gly166=
ENST00000681209.1:c.*262C>A ENSP00000505877.1:n.*262C>A
ENST00000681278.1:n.855C>A
ENST00000681289.1:n.855C>A
ENST00000681361.1:c.*165C>A ENSP00000506679.1:n.*165C>A
ENST00000681430.1:c.498C>A ENSP00000506301.1:p.Gly166=
ENST00000681446.1:c.*80C>A ENSP00000506244.1:n.*80C>A
ENST00000681450.1:c.*169C>A ENSP00000505660.1:n.*169C>A
ENST00000681548.1:c.*84C>A ENSP00000505275.1:n.*84C>A
ENST00000681616.1:c.*266C>A ENSP00000505111.1:n.*266C>A
ENST00000681621.1:c.*82C>A ENSP00000505770.1:n.*82C>A
ENST00000681680.1:n.2622C>A
ENST00000681720.1:c.*55-5797C>A ENSP00000505438.1:n.*55-5797C>A
ENST00000681730.1:n.720C>A
ENST00000681790.1:c.240C>A ENSP00000505130.1:p.Gly80=
ENST00000681837.1:n.1114C>A
ENST00000681913.1:n.2622C>A
ENST00000681916.1:c.*266C>A ENSP00000506477.1:n.*266C>A
ENST00000681930.1:n.2622C>A
ENST00000370834.9:c.597C>A ENSP00000359871.5:p.Gly199=
ENST00000370841.8:c.498C>A ENSP00000359878.4:p.Gly166=
ENST00000420607.6:c.510C>A ENSP00000409612.2:p.Gly170=
ENST00000525808.5:c.*84C>A ENSP00000434823.1:n.*84C>A
ENST00000526129.5:c.*282C>A ENSP00000434092.1:n.*282C>A
ENST00000526196.5:c.*266C>A ENSP00000431953.1:n.*266C>A
ENST00000526930.1:n.271C>A
ENST00000529059.5:n.407C>A
ENST00000530953.6:c.148C>A ENSP00000431372.1:p.Leu50Ile
ENST00000532509.5:c.*262C>A ENSP00000432522.1:n.*262C>A
ENST00000534334.5:c.*82C>A ENSP00000435584.1:n.*82C>A
ENST00000541113.5:c.390C>A ENSP00000442324.1:p.Gly130=
NM_000016.5:c.498C>A NP_000007.1:p.Gly166=
NM_001127328.2:c.510C>A NP_001120800.1:p.Gly170=
NM_001286042.1:c.390C>A NP_001272971.1:p.Gly130=
NM_001286043.1:c.597C>A NP_001272972.1:p.Gly199=
NM_001286044.1:c.-70C>A NP_001272973.1:n.-70C>A
NM_000016.6:c.498C>A MANE Select NP_000007.1:p.Gly166=
NM_001127328.3:c.510C>A NP_001120800.1:p.Gly170=
NM_001286042.2:c.390C>A NP_001272971.1:p.Gly130=
NM_001286043.2:c.597C>A NP_001272972.1:p.Gly199=
NM_001286044.2:c.-70C>A NP_001272973.1:n.-70C>A