Canonical Allele Identifier: CA418544993
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76216138A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750453A>C , CM000663.2:g.75750453A>C GRCh38
NC_000001.10:g.76216138A>C , CM000663.1:g.76216138A>C GRCh37
NC_000001.9:g.75988726A>C NCBI36
NG_007045.2:g.31096A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.852A>C MANE Select ENSP00000359878.5:p.Val284=
ENST00000473018.3:n.2976A>C
ENST00000532207.6:n.1741A>C
ENST00000541113.6:c.849+894A>C ENSP00000442324.2:n.849+894A>C
ENST00000679509.1:n.1814A>C
ENST00000679530.1:c.*620A>C ENSP00000506454.1:n.*620A>C
ENST00000679615.1:n.2867A>C
ENST00000679687.1:c.414A>C ENSP00000506598.1:p.Val138=
ENST00000679704.1:c.*618A>C ENSP00000505117.1:n.*618A>C
ENST00000679709.1:c.*815A>C ENSP00000506623.1:n.*815A>C
ENST00000679976.1:c.*436A>C ENSP00000505565.1:n.*436A>C
ENST00000680166.1:n.4141A>C
ENST00000680315.1:n.735A>C
ENST00000680517.1:c.*240A>C ENSP00000505803.1:n.*240A>C
ENST00000680582.1:n.1814A>C
ENST00000680613.1:c.*223A>C ENSP00000506114.1:n.*223A>C
ENST00000680662.1:c.*766A>C ENSP00000505080.1:n.*766A>C
ENST00000680691.1:c.*515A>C ENSP00000506487.1:n.*515A>C
ENST00000680694.1:c.*440A>C ENSP00000505658.1:n.*440A>C
ENST00000680743.1:c.*519A>C ENSP00000505073.1:n.*519A>C
ENST00000680749.1:c.*137A>C ENSP00000505122.1:n.*137A>C
ENST00000680798.1:c.*327A>C ENSP00000505670.1:n.*327A>C
ENST00000680805.1:c.711A>C ENSP00000505447.1:p.Val237=
ENST00000680844.1:c.*636A>C ENSP00000506541.1:n.*636A>C
ENST00000680948.1:c.*719A>C ENSP00000505441.1:n.*719A>C
ENST00000680964.1:c.852A>C ENSP00000505961.1:p.Val284=
ENST00000681037.1:c.*2336A>C ENSP00000506025.1:n.*2336A>C
ENST00000681063.1:c.602A>C ENSP00000506616.1:p.Ter201Ser
ENST00000681209.1:c.*507A>C ENSP00000505877.1:n.*507A>C
ENST00000681278.1:n.1209A>C
ENST00000681289.1:n.4847A>C
ENST00000681361.1:c.*519A>C ENSP00000506679.1:n.*519A>C
ENST00000681430.1:c.852A>C ENSP00000506301.1:p.Val284=
ENST00000681446.1:c.*434A>C ENSP00000506244.1:n.*434A>C
ENST00000681450.1:c.*523A>C ENSP00000505660.1:n.*523A>C
ENST00000681548.1:c.*438A>C ENSP00000505275.1:n.*438A>C
ENST00000681616.1:c.*511A>C ENSP00000505111.1:n.*511A>C
ENST00000681621.1:c.*436A>C ENSP00000505770.1:n.*436A>C
ENST00000681680.1:n.2947A>C
ENST00000681720.1:c.*307A>C ENSP00000505438.1:n.*307A>C
ENST00000681730.1:n.1074A>C
ENST00000681790.1:c.594A>C ENSP00000505130.1:p.Val198=
ENST00000681837.1:n.1468A>C
ENST00000681913.1:n.2976A>C
ENST00000681916.1:c.*620A>C ENSP00000506477.1:n.*620A>C
ENST00000681930.1:n.2976A>C
ENST00000370834.9:c.951A>C ENSP00000359871.5:p.Val317=
ENST00000370841.8:c.852A>C ENSP00000359878.4:p.Val284=
ENST00000420607.6:c.864A>C ENSP00000409612.2:p.Val288=
ENST00000481374.1:n.3A>C
ENST00000525808.5:c.*438A>C ENSP00000434823.1:n.*438A>C
ENST00000526129.5:c.*636A>C ENSP00000434092.1:n.*636A>C
ENST00000526196.5:c.*620A>C ENSP00000431953.1:n.*620A>C
ENST00000528016.1:c.66A>C ENSP00000434284.1:p.Val22=
ENST00000529059.5:n.761A>C
ENST00000532207.5:n.582A>C
ENST00000534334.5:c.*436A>C ENSP00000435584.1:n.*436A>C
ENST00000541113.5:c.744A>C ENSP00000442324.1:p.Val248=
NM_000016.5:c.852A>C NP_000007.1:p.Val284=
NM_001127328.2:c.864A>C NP_001120800.1:p.Val288=
NM_001286042.1:c.744A>C NP_001272971.1:p.Val248=
NM_001286043.1:c.951A>C NP_001272972.1:p.Val317=
NM_001286044.1:c.285A>C NP_001272973.1:p.Val95=
NM_000016.6:c.852A>C MANE Select NP_000007.1:p.Val284=
NM_001127328.3:c.864A>C NP_001120800.1:p.Val288=
NM_001286042.2:c.744A>C NP_001272971.1:p.Val248=
NM_001286043.2:c.951A>C NP_001272972.1:p.Val317=
NM_001286044.2:c.285A>C NP_001272973.1:p.Val95=