Canonical Allele Identifier: CA418545051
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76216216A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750531A>C , CM000663.2:g.75750531A>C GRCh38
NC_000001.10:g.76216216A>C , CM000663.1:g.76216216A>C GRCh37
NC_000001.9:g.75988804A>C NCBI36
NG_007045.2:g.31174A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.930A>C MANE Select ENSP00000359878.5:p.Gly310=
ENST00000473018.3:n.3054A>C
ENST00000532207.6:n.1819A>C
ENST00000541113.6:c.849+972A>C ENSP00000442324.2:n.849+972A>C
ENST00000679509.1:n.1892A>C
ENST00000679530.1:c.*698A>C ENSP00000506454.1:n.*698A>C
ENST00000679615.1:n.2945A>C
ENST00000679687.1:c.492A>C ENSP00000506598.1:p.Gly164=
ENST00000679704.1:c.*696A>C ENSP00000505117.1:n.*696A>C
ENST00000679709.1:c.*893A>C ENSP00000506623.1:n.*893A>C
ENST00000679976.1:c.*514A>C ENSP00000505565.1:n.*514A>C
ENST00000680166.1:n.4219A>C
ENST00000680315.1:n.813A>C
ENST00000680517.1:c.*318A>C ENSP00000505803.1:n.*318A>C
ENST00000680582.1:n.1892A>C
ENST00000680613.1:c.*301A>C ENSP00000506114.1:n.*301A>C
ENST00000680662.1:c.*844A>C ENSP00000505080.1:n.*844A>C
ENST00000680691.1:c.*593A>C ENSP00000506487.1:n.*593A>C
ENST00000680694.1:c.*518A>C ENSP00000505658.1:n.*518A>C
ENST00000680743.1:c.*597A>C ENSP00000505073.1:n.*597A>C
ENST00000680749.1:c.*215A>C ENSP00000505122.1:n.*215A>C
ENST00000680798.1:c.*405A>C ENSP00000505670.1:n.*405A>C
ENST00000680805.1:c.789A>C ENSP00000505447.1:p.Gly263=
ENST00000680844.1:c.*714A>C ENSP00000506541.1:n.*714A>C
ENST00000680948.1:c.*797A>C ENSP00000505441.1:n.*797A>C
ENST00000680964.1:c.930A>C ENSP00000505961.1:p.Gly310=
ENST00000681037.1:c.*2414A>C ENSP00000506025.1:n.*2414A>C
ENST00000681063.1:c.*77A>C ENSP00000506616.1:n.*77A>C
ENST00000681209.1:c.*585A>C ENSP00000505877.1:n.*585A>C
ENST00000681278.1:n.1287A>C
ENST00000681289.1:n.4925A>C
ENST00000681361.1:c.*597A>C ENSP00000506679.1:n.*597A>C
ENST00000681430.1:c.930A>C ENSP00000506301.1:p.Gly310=
ENST00000681446.1:c.*512A>C ENSP00000506244.1:n.*512A>C
ENST00000681450.1:c.*601A>C ENSP00000505660.1:n.*601A>C
ENST00000681548.1:c.*516A>C ENSP00000505275.1:n.*516A>C
ENST00000681616.1:c.*589A>C ENSP00000505111.1:n.*589A>C
ENST00000681621.1:c.*514A>C ENSP00000505770.1:n.*514A>C
ENST00000681680.1:n.3025A>C
ENST00000681720.1:c.*385A>C ENSP00000505438.1:n.*385A>C
ENST00000681730.1:n.1152A>C
ENST00000681790.1:c.672A>C ENSP00000505130.1:p.Gly224=
ENST00000681837.1:n.1546A>C
ENST00000681913.1:n.3054A>C
ENST00000681916.1:c.*698A>C ENSP00000506477.1:n.*698A>C
ENST00000681930.1:n.3054A>C
ENST00000370834.9:c.1029A>C ENSP00000359871.5:p.Gly343=
ENST00000370841.8:c.930A>C ENSP00000359878.4:p.Gly310=
ENST00000420607.6:c.942A>C ENSP00000409612.2:p.Gly314=
ENST00000481374.1:n.81A>C
ENST00000525808.5:c.*516A>C ENSP00000434823.1:n.*516A>C
ENST00000526129.5:c.*714A>C ENSP00000434092.1:n.*714A>C
ENST00000526196.5:c.*698A>C ENSP00000431953.1:n.*698A>C
ENST00000528016.1:c.144A>C ENSP00000434284.1:p.Gly48=
ENST00000529059.5:n.839A>C
ENST00000532207.5:n.660A>C
ENST00000534334.5:c.*514A>C ENSP00000435584.1:n.*514A>C
ENST00000541113.5:c.822A>C ENSP00000442324.1:p.Gly274=
NM_000016.5:c.930A>C NP_000007.1:p.Gly310=
NM_001127328.2:c.942A>C NP_001120800.1:p.Gly314=
NM_001286042.1:c.822A>C NP_001272971.1:p.Gly274=
NM_001286043.1:c.1029A>C NP_001272972.1:p.Gly343=
NM_001286044.1:c.363A>C NP_001272973.1:p.Gly121=
NM_000016.6:c.930A>C MANE Select NP_000007.1:p.Gly310=
NM_001127328.3:c.942A>C NP_001120800.1:p.Gly314=
NM_001286042.2:c.822A>C NP_001272971.1:p.Gly274=
NM_001286043.2:c.1029A>C NP_001272972.1:p.Gly343=
NM_001286044.2:c.363A>C NP_001272973.1:p.Gly121=