Canonical Allele Identifier: CA1140458951
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750501C= , CM000663.2:g.75750501C= GRCh38
NC_000001.10:g.76216186C= , CM000663.1:g.76216186C= GRCh37
NC_000001.9:g.75988774C= NCBI36
NG_007045.2:g.31144C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.900C= MANE Select ENSP00000359878.5:p.Thr300=
ENST00000473018.3:n.3024C=
ENST00000532207.6:n.1789C=
ENST00000541113.6:c.849+942C= ENSP00000442324.2:n.849+942C=
ENST00000679509.1:n.1862C=
ENST00000679530.1:c.*668C= ENSP00000506454.1:n.*668C=
ENST00000679615.1:n.2915C=
ENST00000679687.1:c.462C= ENSP00000506598.1:p.Thr154=
ENST00000679704.1:c.*666C= ENSP00000505117.1:n.*666C=
ENST00000679709.1:c.*863C= ENSP00000506623.1:n.*863C=
ENST00000679976.1:c.*484C= ENSP00000505565.1:n.*484C=
ENST00000680166.1:n.4189C=
ENST00000680315.1:n.783C=
ENST00000680517.1:c.*288C= ENSP00000505803.1:n.*288C=
ENST00000680582.1:n.1862C=
ENST00000680613.1:c.*271C= ENSP00000506114.1:n.*271C=
ENST00000680662.1:c.*814C= ENSP00000505080.1:n.*814C=
ENST00000680691.1:c.*563C= ENSP00000506487.1:n.*563C=
ENST00000680694.1:c.*488C= ENSP00000505658.1:n.*488C=
ENST00000680743.1:c.*567C= ENSP00000505073.1:n.*567C=
ENST00000680749.1:c.*185C= ENSP00000505122.1:n.*185C=
ENST00000680798.1:c.*375C= ENSP00000505670.1:n.*375C=
ENST00000680805.1:c.759C= ENSP00000505447.1:p.Thr253=
ENST00000680844.1:c.*684C= ENSP00000506541.1:n.*684C=
ENST00000680948.1:c.*767C= ENSP00000505441.1:n.*767C=
ENST00000680964.1:c.900C= ENSP00000505961.1:p.Thr300=
ENST00000681037.1:c.*2384C= ENSP00000506025.1:n.*2384C=
ENST00000681063.1:c.*47C= ENSP00000506616.1:n.*47C=
ENST00000681209.1:c.*555C= ENSP00000505877.1:n.*555C=
ENST00000681278.1:n.1257C=
ENST00000681289.1:n.4895C=
ENST00000681361.1:c.*567C= ENSP00000506679.1:n.*567C=
ENST00000681430.1:c.900C= ENSP00000506301.1:p.Thr300=
ENST00000681446.1:c.*482C= ENSP00000506244.1:n.*482C=
ENST00000681450.1:c.*571C= ENSP00000505660.1:n.*571C=
ENST00000681548.1:c.*486C= ENSP00000505275.1:n.*486C=
ENST00000681616.1:c.*559C= ENSP00000505111.1:n.*559C=
ENST00000681621.1:c.*484C= ENSP00000505770.1:n.*484C=
ENST00000681680.1:n.2995C=
ENST00000681720.1:c.*355C= ENSP00000505438.1:n.*355C=
ENST00000681730.1:n.1122C=
ENST00000681790.1:c.642C= ENSP00000505130.1:p.Thr214=
ENST00000681837.1:n.1516C=
ENST00000681913.1:n.3024C=
ENST00000681916.1:c.*668C= ENSP00000506477.1:n.*668C=
ENST00000681930.1:n.3024C=
ENST00000370834.9:c.999C= ENSP00000359871.5:p.Thr333=
ENST00000370841.8:c.900C= ENSP00000359878.4:p.Thr300=
ENST00000420607.6:c.912C= ENSP00000409612.2:p.Thr304=
ENST00000481374.1:n.51C=
ENST00000525808.5:c.*486C= ENSP00000434823.1:n.*486C=
ENST00000526129.5:c.*684C= ENSP00000434092.1:n.*684C=
ENST00000526196.5:c.*668C= ENSP00000431953.1:n.*668C=
ENST00000528016.1:c.114C= ENSP00000434284.1:p.Thr38=
ENST00000529059.5:n.809C=
ENST00000532207.5:n.630C=
ENST00000534334.5:c.*484C= ENSP00000435584.1:n.*484C=
ENST00000541113.5:c.792C= ENSP00000442324.1:p.Thr264=
NM_000016.5:c.900C= NP_000007.1:p.Thr300=
NM_001127328.2:c.912C= NP_001120800.1:p.Thr304=
NM_001286042.1:c.792C= NP_001272971.1:p.Thr264=
NM_001286043.1:c.999C= NP_001272972.1:p.Thr333=
NM_001286044.1:c.333C= NP_001272973.1:p.Thr111=
NM_000016.6:c.900C= MANE Select NP_000007.1:p.Thr300=
NM_001127328.3:c.912C= NP_001120800.1:p.Thr304=
NM_001286042.2:c.792C= NP_001272971.1:p.Thr264=
NM_001286043.2:c.999C= NP_001272972.1:p.Thr333=
NM_001286044.2:c.333C= NP_001272973.1:p.Thr111=