Canonical Allele Identifier: CA1176711072
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75735132G= , CM000663.2:g.75735132G= GRCh38
NC_000001.10:g.76200817G= , CM000663.1:g.76200817G= GRCh37
NC_000001.9:g.75973405G= NCBI36
NG_007045.2:g.15775G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.468+261G= MANE Select ENSP00000359878.5:n.468+261G=
ENST00000473018.3:n.2592+261G=
ENST00000541113.6:c.468+261G= ENSP00000442324.2:n.468+261G=
ENST00000679509.1:n.1430+261G=
ENST00000679530.1:c.*236+261G= ENSP00000506454.1:n.*236+261G=
ENST00000679615.1:n.2592+261G=
ENST00000679687.1:c.31-4848G= ENSP00000506598.1:n.31-4848G=
ENST00000679704.1:c.*234+261G= ENSP00000505117.1:n.*234+261G=
ENST00000679709.1:c.*431+261G= ENSP00000506623.1:n.*431+261G=
ENST00000679804.1:n.207+2210G=
ENST00000679976.1:c.*52+261G= ENSP00000505565.1:n.*52+261G=
ENST00000680166.1:n.3757+261G=
ENST00000680517.1:c.286+2210G= ENSP00000505803.1:n.286+2210G=
ENST00000680582.1:n.1430+261G=
ENST00000680613.1:c.468+261G= ENSP00000506114.1:n.468+261G=
ENST00000680662.1:c.*382+261G= ENSP00000505080.1:n.*382+261G=
ENST00000680691.1:c.*131+261G= ENSP00000506487.1:n.*131+261G=
ENST00000680694.1:c.*56+257G= ENSP00000505658.1:n.*56+257G=
ENST00000680743.1:c.*135+261G= ENSP00000505073.1:n.*135+261G=
ENST00000680749.1:c.468+261G= ENSP00000505122.1:n.468+261G=
ENST00000680798.1:c.*52+261G= ENSP00000505670.1:n.*52+261G=
ENST00000680805.1:c.468+261G= ENSP00000505447.1:n.468+261G=
ENST00000680844.1:c.*252+261G= ENSP00000506541.1:n.*252+261G=
ENST00000680948.1:c.*335+261G= ENSP00000505441.1:n.*335+261G=
ENST00000680964.1:c.468+261G= ENSP00000505961.1:n.468+261G=
ENST00000681037.1:c.468+261G= ENSP00000506025.1:n.468+261G=
ENST00000681063.1:c.468+261G= ENSP00000506616.1:n.468+261G=
ENST00000681209.1:c.*232+261G= ENSP00000505877.1:n.*232+261G=
ENST00000681278.1:n.825+261G=
ENST00000681289.1:n.825+261G=
ENST00000681361.1:c.*135+261G= ENSP00000506679.1:n.*135+261G=
ENST00000681430.1:c.468+261G= ENSP00000506301.1:n.468+261G=
ENST00000681446.1:c.*50+263G= ENSP00000506244.1:n.*50+263G=
ENST00000681450.1:c.*139+257G= ENSP00000505660.1:n.*139+257G=
ENST00000681548.1:c.*54+2210G= ENSP00000505275.1:n.*54+2210G=
ENST00000681616.1:c.*236+261G= ENSP00000505111.1:n.*236+261G=
ENST00000681621.1:c.*52+261G= ENSP00000505770.1:n.*52+261G=
ENST00000681680.1:n.2592+261G=
ENST00000681720.1:c.*54+2210G= ENSP00000505438.1:n.*54+2210G=
ENST00000681730.1:n.690+261G=
ENST00000681790.1:c.210+261G= ENSP00000505130.1:n.210+261G=
ENST00000681837.1:n.1084+261G=
ENST00000681913.1:n.2592+261G=
ENST00000681916.1:c.*236+261G= ENSP00000506477.1:n.*236+261G=
ENST00000681930.1:n.2592+261G=
ENST00000370834.9:c.567+261G= ENSP00000359871.5:n.567+261G=
ENST00000370841.8:c.468+261G= ENSP00000359878.4:n.468+261G=
ENST00000420607.6:c.480+261G= ENSP00000409612.2:n.480+261G=
ENST00000525808.5:c.*54+2210G= ENSP00000434823.1:n.*54+2210G=
ENST00000526129.5:c.*252+261G= ENSP00000434092.1:n.*252+261G=
ENST00000526196.5:c.*236+261G= ENSP00000431953.1:n.*236+261G=
ENST00000526930.1:n.241+261G=
ENST00000529059.5:n.377+261G=
ENST00000530953.6:c.119-4848G= ENSP00000431372.1:n.119-4848G=
ENST00000532509.5:c.*232+261G= ENSP00000432522.1:n.*232+261G=
ENST00000534334.5:c.*52+261G= ENSP00000435584.1:n.*52+261G=
ENST00000541113.5:c.360+261G= ENSP00000442324.1:n.360+261G=
NM_000016.5:c.468+261G= NP_000007.1:n.468+261G=
NM_001127328.2:c.480+261G= NP_001120800.1:n.480+261G=
NM_001286042.1:c.360+261G= NP_001272971.1:n.360+261G=
NM_001286043.1:c.567+261G= NP_001272972.1:n.567+261G=
NM_001286044.1:c.-100+2210G= NP_001272973.1:n.-100+2210G=
NM_000016.6:c.468+261G= MANE Select NP_000007.1:n.468+261G=
NM_001127328.3:c.480+261G= NP_001120800.1:n.480+261G=
NM_001286042.2:c.360+261G= NP_001272971.1:n.360+261G=
NM_001286043.2:c.567+261G= NP_001272972.1:n.567+261G=
NM_001286044.2:c.-100+2210G= NP_001272973.1:n.-100+2210G=