Canonical Allele Identifier: CA418544838
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76215160G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749475G>A , CM000663.2:g.75749475G>A GRCh38
NC_000001.10:g.76215160G>A , CM000663.1:g.76215160G>A GRCh37
NC_000001.9:g.75987748G>A NCBI36
NG_007045.2:g.30118G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.765G>A MANE Select ENSP00000359878.5:p.Val255=
ENST00000473018.3:n.2889G>A
ENST00000532207.6:n.1654G>A
ENST00000541113.6:c.765G>A ENSP00000442324.2:p.Val255=
ENST00000679509.1:n.1727G>A
ENST00000679530.1:c.*533G>A ENSP00000506454.1:n.*533G>A
ENST00000679615.1:n.2780G>A
ENST00000679687.1:c.327G>A ENSP00000506598.1:p.Val109=
ENST00000679704.1:c.*531G>A ENSP00000505117.1:n.*531G>A
ENST00000679709.1:c.*728G>A ENSP00000506623.1:n.*728G>A
ENST00000679976.1:c.*349G>A ENSP00000505565.1:n.*349G>A
ENST00000680166.1:n.4054G>A
ENST00000680517.1:c.*153G>A ENSP00000505803.1:n.*153G>A
ENST00000680582.1:n.1727G>A
ENST00000680613.1:c.*136G>A ENSP00000506114.1:n.*136G>A
ENST00000680662.1:c.*679G>A ENSP00000505080.1:n.*679G>A
ENST00000680691.1:c.*428G>A ENSP00000506487.1:n.*428G>A
ENST00000680694.1:c.*353G>A ENSP00000505658.1:n.*353G>A
ENST00000680743.1:c.*432G>A ENSP00000505073.1:n.*432G>A
ENST00000680749.1:c.*50G>A ENSP00000505122.1:n.*50G>A
ENST00000680798.1:c.*240G>A ENSP00000505670.1:n.*240G>A
ENST00000680805.1:c.709-976G>A ENSP00000505447.1:n.709-976G>A
ENST00000680844.1:c.*549G>A ENSP00000506541.1:n.*549G>A
ENST00000680948.1:c.*632G>A ENSP00000505441.1:n.*632G>A
ENST00000680964.1:c.765G>A ENSP00000505961.1:p.Val255=
ENST00000681037.1:c.*2249G>A ENSP00000506025.1:n.*2249G>A
ENST00000681063.1:c.600-976G>A ENSP00000506616.1:n.600-976G>A
ENST00000681209.1:c.*420G>A ENSP00000505877.1:n.*420G>A
ENST00000681278.1:n.1122G>A
ENST00000681289.1:n.4760G>A
ENST00000681361.1:c.*432G>A ENSP00000506679.1:n.*432G>A
ENST00000681430.1:c.765G>A ENSP00000506301.1:p.Val255=
ENST00000681446.1:c.*347G>A ENSP00000506244.1:n.*347G>A
ENST00000681450.1:c.*436G>A ENSP00000505660.1:n.*436G>A
ENST00000681548.1:c.*351G>A ENSP00000505275.1:n.*351G>A
ENST00000681616.1:c.*424G>A ENSP00000505111.1:n.*424G>A
ENST00000681621.1:c.*349G>A ENSP00000505770.1:n.*349G>A
ENST00000681680.1:n.2860G>A
ENST00000681720.1:c.*220G>A ENSP00000505438.1:n.*220G>A
ENST00000681730.1:n.987G>A
ENST00000681790.1:c.507G>A ENSP00000505130.1:p.Val169=
ENST00000681837.1:n.1381G>A
ENST00000681913.1:n.2889G>A
ENST00000681916.1:c.*533G>A ENSP00000506477.1:n.*533G>A
ENST00000681930.1:n.2889G>A
ENST00000370834.9:c.864G>A ENSP00000359871.5:p.Val288=
ENST00000370841.8:c.765G>A ENSP00000359878.4:p.Val255=
ENST00000420607.6:c.777G>A ENSP00000409612.2:p.Val259=
ENST00000525808.5:c.*351G>A ENSP00000434823.1:n.*351G>A
ENST00000526129.5:c.*549G>A ENSP00000434092.1:n.*549G>A
ENST00000526196.5:c.*533G>A ENSP00000431953.1:n.*533G>A
ENST00000526930.1:n.538G>A
ENST00000529059.5:n.674G>A
ENST00000530953.6:c.*262G>A ENSP00000431372.1:n.*262G>A
ENST00000532207.5:n.495G>A
ENST00000532509.5:c.*529G>A ENSP00000432522.1:n.*529G>A
ENST00000534334.5:c.*349G>A ENSP00000435584.1:n.*349G>A
ENST00000541113.5:c.657G>A ENSP00000442324.1:p.Val219=
NM_000016.5:c.765G>A NP_000007.1:p.Val255=
NM_001127328.2:c.777G>A NP_001120800.1:p.Val259=
NM_001286042.1:c.657G>A NP_001272971.1:p.Val219=
NM_001286043.1:c.864G>A NP_001272972.1:p.Val288=
NM_001286044.1:c.198G>A NP_001272973.1:p.Val66=
NM_000016.6:c.765G>A MANE Select NP_000007.1:p.Val255=
NM_001127328.3:c.777G>A NP_001120800.1:p.Val259=
NM_001286042.2:c.657G>A NP_001272971.1:p.Val219=
NM_001286043.2:c.864G>A NP_001272972.1:p.Val288=
NM_001286044.2:c.198G>A NP_001272973.1:p.Val66=