Canonical Allele Identifier: CA2831039317
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75732878_75732879insT , CM000663.2:g.75732878_75732879insT GRCh38
NC_000001.10:g.76198563_76198564insT , CM000663.1:g.76198563_76198564insT GRCh37
NC_000001.9:g.75971151_75971152insT NCBI36
NG_007045.2:g.13521_13522insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.242_243insT MANE Select ENSP00000359878.5:p.Trp82LeufsTer23
ENST00000473018.3:n.599_600insT
ENST00000525881.6:n.599_600insT
ENST00000541113.6:c.242_243insT ENSP00000442324.2:p.Trp82LeufsTer23
ENST00000679509.1:n.599_600insT
ENST00000679530.1:c.*10_*11insT ENSP00000506454.1:n.*10_*11insT
ENST00000679615.1:n.599_600insT
ENST00000679687.1:c.31-7102_31-7101insT ENSP00000506598.1:n.31-7102_31-7101insT
ENST00000679704.1:c.*10_*11insT ENSP00000505117.1:n.*10_*11insT
ENST00000679709.1:c.*205_*206insT ENSP00000506623.1:n.*205_*206insT
ENST00000679804.1:n.163_164insT
ENST00000679976.1:c.242_243insT ENSP00000505565.1:p.Trp82LeufsTer?
ENST00000680166.1:n.1764_1765insT
ENST00000680517.1:c.242_243insT ENSP00000505803.1:p.Trp82LeufsTer19
ENST00000680582.1:n.599_600insT
ENST00000680613.1:c.242_243insT ENSP00000506114.1:p.Trp82LeufsTer23
ENST00000680662.1:c.*156_*157insT ENSP00000505080.1:n.*156_*157insT
ENST00000680691.1:c.*6_*7insT ENSP00000506487.1:n.*6_*7insT
ENST00000680694.1:c.242_243insT ENSP00000505658.1:p.Trp82LeufsTer?
ENST00000680743.1:c.*10_*11insT ENSP00000505073.1:n.*10_*11insT
ENST00000680749.1:c.242_243insT ENSP00000505122.1:p.Trp82LeufsTer23
ENST00000680798.1:c.242_243insT ENSP00000505670.1:p.Trp82LeufsTer?
ENST00000680805.1:c.242_243insT ENSP00000505447.1:p.Trp82LeufsTer23
ENST00000680844.1:c.*26_*27insT ENSP00000506541.1:n.*26_*27insT
ENST00000680948.1:c.*10_*11insT ENSP00000505441.1:n.*10_*11insT
ENST00000680964.1:c.242_243insT ENSP00000505961.1:p.Trp82LeufsTer23
ENST00000681037.1:c.242_243insT ENSP00000506025.1:p.Trp82LeufsTer23
ENST00000681063.1:c.242_243insT ENSP00000506616.1:p.Trp82LeufsTer23
ENST00000681209.1:c.*6_*7insT ENSP00000505877.1:n.*6_*7insT
ENST00000681278.1:n.599_600insT
ENST00000681289.1:n.599_600insT
ENST00000681361.1:c.*10_*11insT ENSP00000506679.1:n.*10_*11insT
ENST00000681430.1:c.242_243insT ENSP00000506301.1:p.Trp82LeufsTer23
ENST00000681446.1:c.242_243insT ENSP00000506244.1:p.Trp82LeufsTer?
ENST00000681450.1:c.*10_*11insT ENSP00000505660.1:n.*10_*11insT
ENST00000681548.1:c.*10_*11insT ENSP00000505275.1:n.*10_*11insT
ENST00000681616.1:c.*10_*11insT ENSP00000505111.1:n.*10_*11insT
ENST00000681621.1:c.242_243insT ENSP00000505770.1:p.Trp82LeufsTer?
ENST00000681680.1:n.599_600insT
ENST00000681720.1:c.*10_*11insT ENSP00000505438.1:n.*10_*11insT
ENST00000681730.1:n.464_465insT
ENST00000681790.1:c.-17_-16insT ENSP00000505130.1:n.-17_-16insT
ENST00000681837.1:n.253_254insT
ENST00000681913.1:n.599_600insT
ENST00000681916.1:c.*10_*11insT ENSP00000506477.1:n.*10_*11insT
ENST00000681930.1:n.599_600insT
ENST00000370834.9:c.242_243insT ENSP00000359871.5:p.Trp82LeufsTer15
ENST00000370841.8:c.242_243insT ENSP00000359878.4:p.Trp82LeufsTer23
ENST00000420607.6:c.254_255insT ENSP00000409612.2:p.Trp86LeufsTer23
ENST00000473018.2:n.275_276insT
ENST00000525808.5:c.*10_*11insT ENSP00000434823.1:n.*10_*11insT
ENST00000525881.5:n.251_252insT
ENST00000526129.5:c.*26_*27insT ENSP00000434092.1:n.*26_*27insT
ENST00000526196.5:c.*10_*11insT ENSP00000431953.1:n.*10_*11insT
ENST00000529059.5:n.252_253insT
ENST00000530953.6:c.118+4390_118+4391insT ENSP00000431372.1:n.118+4390_118+4391insT
ENST00000532509.5:c.*6_*7insT ENSP00000432522.1:n.*6_*7insT
ENST00000534146.5:n.321_322insT
ENST00000534334.5:c.242_243insT ENSP00000435584.1:p.Trp82LeufsTer?
ENST00000541113.5:c.134_135insT ENSP00000442324.1:p.Trp46LeufsTer23
NM_000016.5:c.242_243insT NP_000007.1:p.Trp82LeufsTer23
NM_001127328.2:c.254_255insT NP_001120800.1:p.Trp86LeufsTer23
NM_001286042.1:c.134_135insT NP_001272971.1:p.Trp46LeufsTer23
NM_001286043.1:c.242_243insT NP_001272972.1:p.Trp82LeufsTer15
NM_001286044.1:c.-144_-143insT NP_001272973.1:n.-144_-143insT
NM_000016.6:c.242_243insT MANE Select NP_000007.1:p.Trp82LeufsTer23
NM_001127328.3:c.254_255insT NP_001120800.1:p.Trp86LeufsTer23
NM_001286042.2:c.134_135insT NP_001272971.1:p.Trp46LeufsTer23
NM_001286043.2:c.242_243insT NP_001272972.1:p.Trp82LeufsTer15
NM_001286044.2:c.-144_-143insT NP_001272973.1:n.-144_-143insT