Canonical Allele Identifier: CA340818222
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761303T>A , CM000663.2:g.75761303T>A GRCh38
NC_000001.10:g.76226988T>A , CM000663.1:g.76226988T>A GRCh37
NC_000001.9:g.75999576T>A NCBI36
NG_007045.2:g.41946T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1127T>A MANE Select ENSP00000359878.5:p.Leu376His
ENST00000473018.3:n.3251T>A
ENST00000532207.6:n.2138T>A
ENST00000541113.6:c.1031T>A ENSP00000442324.2:p.Leu344His
ENST00000679509.1:n.2089T>A
ENST00000679530.1:c.*895T>A ENSP00000506454.1:n.*895T>A
ENST00000679615.1:n.3142T>A
ENST00000679687.1:c.689T>A ENSP00000506598.1:p.Leu230His
ENST00000679704.1:c.*893T>A ENSP00000505117.1:n.*893T>A
ENST00000679709.1:c.*1090T>A ENSP00000506623.1:n.*1090T>A
ENST00000679976.1:c.*711T>A ENSP00000505565.1:n.*711T>A
ENST00000680166.1:n.4416T>A
ENST00000680315.1:n.1010T>A
ENST00000680517.1:c.*515T>A ENSP00000505803.1:n.*515T>A
ENST00000680582.1:n.2089T>A
ENST00000680613.1:c.*620T>A ENSP00000506114.1:n.*620T>A
ENST00000680662.1:c.*1041T>A ENSP00000505080.1:n.*1041T>A
ENST00000680691.1:c.*790T>A ENSP00000506487.1:n.*790T>A
ENST00000680694.1:c.*715T>A ENSP00000505658.1:n.*715T>A
ENST00000680743.1:c.*916T>A ENSP00000505073.1:n.*916T>A
ENST00000680749.1:c.*412T>A ENSP00000505122.1:n.*412T>A
ENST00000680798.1:c.*602T>A ENSP00000505670.1:n.*602T>A
ENST00000680805.1:c.986T>A ENSP00000505447.1:p.Leu329His
ENST00000680844.1:c.*911T>A ENSP00000506541.1:n.*911T>A
ENST00000680948.1:c.*994T>A ENSP00000505441.1:n.*994T>A
ENST00000680964.1:c.*220T>A ENSP00000505961.1:n.*220T>A
ENST00000681037.1:c.*2611T>A ENSP00000506025.1:n.*2611T>A
ENST00000681063.1:c.*396T>A ENSP00000506616.1:n.*396T>A
ENST00000681209.1:c.*782T>A ENSP00000505877.1:n.*782T>A
ENST00000681278.1:n.1829T>A
ENST00000681289.1:n.5122T>A
ENST00000681361.1:c.*794T>A ENSP00000506679.1:n.*794T>A
ENST00000681430.1:c.*220T>A ENSP00000506301.1:n.*220T>A
ENST00000681446.1:c.*831T>A ENSP00000506244.1:n.*831T>A
ENST00000681450.1:c.*798T>A ENSP00000505660.1:n.*798T>A
ENST00000681548.1:c.*713T>A ENSP00000505275.1:n.*713T>A
ENST00000681616.1:c.*786T>A ENSP00000505111.1:n.*786T>A
ENST00000681621.1:c.*711T>A ENSP00000505770.1:n.*711T>A
ENST00000681680.1:n.3222T>A
ENST00000681720.1:c.*582T>A ENSP00000505438.1:n.*582T>A
ENST00000681730.1:n.1349T>A
ENST00000681790.1:c.869T>A ENSP00000505130.1:p.Leu290His
ENST00000681837.1:n.1743T>A
ENST00000681913.1:n.3373T>A
ENST00000681916.1:c.*895T>A ENSP00000506477.1:n.*895T>A
ENST00000681930.1:n.3251T>A
ENST00000370834.9:c.1226T>A ENSP00000359871.5:p.Leu409His
ENST00000370841.8:c.1127T>A ENSP00000359878.4:p.Leu376His
ENST00000420607.6:c.1139T>A ENSP00000409612.2:p.Leu380His
ENST00000481374.1:n.400T>A
ENST00000525808.5:c.*713T>A ENSP00000434823.1:n.*713T>A
ENST00000526129.5:c.*911T>A ENSP00000434092.1:n.*911T>A
ENST00000526196.5:c.*895T>A ENSP00000431953.1:n.*895T>A
ENST00000528016.1:c.160-7874T>A ENSP00000434284.1:n.160-7874T>A
ENST00000529059.5:n.1036T>A
ENST00000541113.5:c.1019T>A ENSP00000442324.1:p.Leu340His
NM_000016.5:c.1127T>A NP_000007.1:p.Leu376His
NM_001127328.2:c.1139T>A NP_001120800.1:p.Leu380His
NM_001286042.1:c.1019T>A NP_001272971.1:p.Leu340His
NM_001286043.1:c.1226T>A NP_001272972.1:p.Leu409His
NM_001286044.1:c.560T>A NP_001272973.1:p.Leu187His
NM_000016.6:c.1127T>A MANE Select NP_000007.1:p.Leu376His
NM_001127328.3:c.1139T>A NP_001120800.1:p.Leu380His
NM_001286042.2:c.1019T>A NP_001272971.1:p.Leu340His
NM_001286043.2:c.1226T>A NP_001272972.1:p.Leu409His
NM_001286044.2:c.560T>A NP_001272973.1:p.Leu187His