Canonical Allele Identifier: CA340817998
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761194G>C , CM000663.2:g.75761194G>C GRCh38
NC_000001.10:g.76226879G>C , CM000663.1:g.76226879G>C GRCh37
NC_000001.9:g.75999467G>C NCBI36
NG_007045.2:g.41837G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1018G>C MANE Select ENSP00000359878.5:p.Ala340Pro
ENST00000473018.3:n.3142G>C
ENST00000532207.6:n.2029G>C
ENST00000541113.6:c.922G>C ENSP00000442324.2:p.Ala308Pro
ENST00000679509.1:n.1980G>C
ENST00000679530.1:c.*786G>C ENSP00000506454.1:n.*786G>C
ENST00000679615.1:n.3033G>C
ENST00000679687.1:c.580G>C ENSP00000506598.1:p.Ala194Pro
ENST00000679704.1:c.*784G>C ENSP00000505117.1:n.*784G>C
ENST00000679709.1:c.*981G>C ENSP00000506623.1:n.*981G>C
ENST00000679976.1:c.*602G>C ENSP00000505565.1:n.*602G>C
ENST00000680166.1:n.4307G>C
ENST00000680315.1:n.901G>C
ENST00000680517.1:c.*406G>C ENSP00000505803.1:n.*406G>C
ENST00000680582.1:n.1980G>C
ENST00000680613.1:c.*511G>C ENSP00000506114.1:n.*511G>C
ENST00000680662.1:c.*932G>C ENSP00000505080.1:n.*932G>C
ENST00000680691.1:c.*681G>C ENSP00000506487.1:n.*681G>C
ENST00000680694.1:c.*606G>C ENSP00000505658.1:n.*606G>C
ENST00000680743.1:c.*807G>C ENSP00000505073.1:n.*807G>C
ENST00000680749.1:c.*303G>C ENSP00000505122.1:n.*303G>C
ENST00000680798.1:c.*493G>C ENSP00000505670.1:n.*493G>C
ENST00000680805.1:c.877G>C ENSP00000505447.1:p.Ala293Pro
ENST00000680844.1:c.*802G>C ENSP00000506541.1:n.*802G>C
ENST00000680948.1:c.*885G>C ENSP00000505441.1:n.*885G>C
ENST00000680964.1:c.*111G>C ENSP00000505961.1:n.*111G>C
ENST00000681037.1:c.*2502G>C ENSP00000506025.1:n.*2502G>C
ENST00000681063.1:c.*287G>C ENSP00000506616.1:n.*287G>C
ENST00000681209.1:c.*673G>C ENSP00000505877.1:n.*673G>C
ENST00000681278.1:n.1720G>C
ENST00000681289.1:n.5013G>C
ENST00000681361.1:c.*685G>C ENSP00000506679.1:n.*685G>C
ENST00000681430.1:c.*111G>C ENSP00000506301.1:n.*111G>C
ENST00000681446.1:c.*722G>C ENSP00000506244.1:n.*722G>C
ENST00000681450.1:c.*689G>C ENSP00000505660.1:n.*689G>C
ENST00000681548.1:c.*604G>C ENSP00000505275.1:n.*604G>C
ENST00000681616.1:c.*677G>C ENSP00000505111.1:n.*677G>C
ENST00000681621.1:c.*602G>C ENSP00000505770.1:n.*602G>C
ENST00000681680.1:n.3113G>C
ENST00000681720.1:c.*473G>C ENSP00000505438.1:n.*473G>C
ENST00000681730.1:n.1240G>C
ENST00000681790.1:c.760G>C ENSP00000505130.1:p.Ala254Pro
ENST00000681837.1:n.1634G>C
ENST00000681913.1:n.3264G>C
ENST00000681916.1:c.*786G>C ENSP00000506477.1:n.*786G>C
ENST00000681930.1:n.3142G>C
ENST00000370834.9:c.1117G>C ENSP00000359871.5:p.Ala373Pro
ENST00000370841.8:c.1018G>C ENSP00000359878.4:p.Ala340Pro
ENST00000420607.6:c.1030G>C ENSP00000409612.2:p.Ala344Pro
ENST00000481374.1:n.291G>C
ENST00000525808.5:c.*604G>C ENSP00000434823.1:n.*604G>C
ENST00000526129.5:c.*802G>C ENSP00000434092.1:n.*802G>C
ENST00000526196.5:c.*786G>C ENSP00000431953.1:n.*786G>C
ENST00000528016.1:c.160-7983G>C ENSP00000434284.1:n.160-7983G>C
ENST00000529059.5:n.927G>C
ENST00000532207.5:n.748G>C
ENST00000534334.5:c.*759G>C ENSP00000435584.1:n.*759G>C
ENST00000541113.5:c.910G>C ENSP00000442324.1:p.Ala304Pro
NM_000016.5:c.1018G>C NP_000007.1:p.Ala340Pro
NM_001127328.2:c.1030G>C NP_001120800.1:p.Ala344Pro
NM_001286042.1:c.910G>C NP_001272971.1:p.Ala304Pro
NM_001286043.1:c.1117G>C NP_001272972.1:p.Ala373Pro
NM_001286044.1:c.451G>C NP_001272973.1:p.Ala151Pro
NM_000016.6:c.1018G>C MANE Select NP_000007.1:p.Ala340Pro
NM_001127328.3:c.1030G>C NP_001120800.1:p.Ala344Pro
NM_001286042.2:c.910G>C NP_001272971.1:p.Ala304Pro
NM_001286043.2:c.1117G>C NP_001272972.1:p.Ala373Pro
NM_001286044.2:c.451G>C NP_001272973.1:p.Ala151Pro