Canonical Allele Identifier: CA340818021
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761205G>C , CM000663.2:g.75761205G>C GRCh38
NC_000001.10:g.76226890G>C , CM000663.1:g.76226890G>C GRCh37
NC_000001.9:g.75999478G>C NCBI36
NG_007045.2:g.41848G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1029G>C MANE Select ENSP00000359878.5:p.Glu343Asp
ENST00000473018.3:n.3153G>C
ENST00000532207.6:n.2040G>C
ENST00000541113.6:c.933G>C ENSP00000442324.2:p.Glu311Asp
ENST00000679509.1:n.1991G>C
ENST00000679530.1:c.*797G>C ENSP00000506454.1:n.*797G>C
ENST00000679615.1:n.3044G>C
ENST00000679687.1:c.591G>C ENSP00000506598.1:p.Glu197Asp
ENST00000679704.1:c.*795G>C ENSP00000505117.1:n.*795G>C
ENST00000679709.1:c.*992G>C ENSP00000506623.1:n.*992G>C
ENST00000679976.1:c.*613G>C ENSP00000505565.1:n.*613G>C
ENST00000680166.1:n.4318G>C
ENST00000680315.1:n.912G>C
ENST00000680517.1:c.*417G>C ENSP00000505803.1:n.*417G>C
ENST00000680582.1:n.1991G>C
ENST00000680613.1:c.*522G>C ENSP00000506114.1:n.*522G>C
ENST00000680662.1:c.*943G>C ENSP00000505080.1:n.*943G>C
ENST00000680691.1:c.*692G>C ENSP00000506487.1:n.*692G>C
ENST00000680694.1:c.*617G>C ENSP00000505658.1:n.*617G>C
ENST00000680743.1:c.*818G>C ENSP00000505073.1:n.*818G>C
ENST00000680749.1:c.*314G>C ENSP00000505122.1:n.*314G>C
ENST00000680798.1:c.*504G>C ENSP00000505670.1:n.*504G>C
ENST00000680805.1:c.888G>C ENSP00000505447.1:p.Glu296Asp
ENST00000680844.1:c.*813G>C ENSP00000506541.1:n.*813G>C
ENST00000680948.1:c.*896G>C ENSP00000505441.1:n.*896G>C
ENST00000680964.1:c.*122G>C ENSP00000505961.1:n.*122G>C
ENST00000681037.1:c.*2513G>C ENSP00000506025.1:n.*2513G>C
ENST00000681063.1:c.*298G>C ENSP00000506616.1:n.*298G>C
ENST00000681209.1:c.*684G>C ENSP00000505877.1:n.*684G>C
ENST00000681278.1:n.1731G>C
ENST00000681289.1:n.5024G>C
ENST00000681361.1:c.*696G>C ENSP00000506679.1:n.*696G>C
ENST00000681430.1:c.*122G>C ENSP00000506301.1:n.*122G>C
ENST00000681446.1:c.*733G>C ENSP00000506244.1:n.*733G>C
ENST00000681450.1:c.*700G>C ENSP00000505660.1:n.*700G>C
ENST00000681548.1:c.*615G>C ENSP00000505275.1:n.*615G>C
ENST00000681616.1:c.*688G>C ENSP00000505111.1:n.*688G>C
ENST00000681621.1:c.*613G>C ENSP00000505770.1:n.*613G>C
ENST00000681680.1:n.3124G>C
ENST00000681720.1:c.*484G>C ENSP00000505438.1:n.*484G>C
ENST00000681730.1:n.1251G>C
ENST00000681790.1:c.771G>C ENSP00000505130.1:p.Glu257Asp
ENST00000681837.1:n.1645G>C
ENST00000681913.1:n.3275G>C
ENST00000681916.1:c.*797G>C ENSP00000506477.1:n.*797G>C
ENST00000681930.1:n.3153G>C
ENST00000370834.9:c.1128G>C ENSP00000359871.5:p.Glu376Asp
ENST00000370841.8:c.1029G>C ENSP00000359878.4:p.Glu343Asp
ENST00000420607.6:c.1041G>C ENSP00000409612.2:p.Glu347Asp
ENST00000481374.1:n.302G>C
ENST00000525808.5:c.*615G>C ENSP00000434823.1:n.*615G>C
ENST00000526129.5:c.*813G>C ENSP00000434092.1:n.*813G>C
ENST00000526196.5:c.*797G>C ENSP00000431953.1:n.*797G>C
ENST00000528016.1:c.160-7972G>C ENSP00000434284.1:n.160-7972G>C
ENST00000529059.5:n.938G>C
ENST00000532207.5:n.759G>C
ENST00000534334.5:c.*770G>C ENSP00000435584.1:n.*770G>C
ENST00000541113.5:c.921G>C ENSP00000442324.1:p.Glu307Asp
NM_000016.5:c.1029G>C NP_000007.1:p.Glu343Asp
NM_001127328.2:c.1041G>C NP_001120800.1:p.Glu347Asp
NM_001286042.1:c.921G>C NP_001272971.1:p.Glu307Asp
NM_001286043.1:c.1128G>C NP_001272972.1:p.Glu376Asp
NM_001286044.1:c.462G>C NP_001272973.1:p.Glu154Asp
NM_000016.6:c.1029G>C MANE Select NP_000007.1:p.Glu343Asp
NM_001127328.3:c.1041G>C NP_001120800.1:p.Glu347Asp
NM_001286042.2:c.921G>C NP_001272971.1:p.Glu307Asp
NM_001286043.2:c.1128G>C NP_001272972.1:p.Glu376Asp
NM_001286044.2:c.462G>C NP_001272973.1:p.Glu154Asp