Canonical Allele Identifier: CA2573132608
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 1457250
ClinVar RCV Id: RCV001953660
dbSNP Id: rs2100417619

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749488_75749492del , CM000663.2:g.75749488_75749492del GRCh38
NC_000001.10:g.76215173_76215177del , CM000663.1:g.76215173_76215177del GRCh37
NC_000001.9:g.75987761_75987765del NCBI36
NG_007045.2:g.30131_30135del

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.778_782del MANE Select ENSP00000359878.5:p.Glu260CysfsTer5
ENST00000473018.3:n.2902_2906del
ENST00000532207.6:n.1667_1671del
ENST00000541113.6:c.778_782del ENSP00000442324.2:p.Glu260CysfsTer5
ENST00000679509.1:n.1740_1744del
ENST00000679530.1:c.*546_*550del ENSP00000506454.1:n.*546_*550del
ENST00000679615.1:n.2793_2797del
ENST00000679687.1:c.340_344del ENSP00000506598.1:p.Glu114CysfsTer5
ENST00000679704.1:c.*544_*548del ENSP00000505117.1:n.*544_*548del
ENST00000679709.1:c.*741_*745del ENSP00000506623.1:n.*741_*745del
ENST00000679976.1:c.*362_*366del ENSP00000505565.1:n.*362_*366del
ENST00000680166.1:n.4067_4071del
ENST00000680517.1:c.*166_*170del ENSP00000505803.1:n.*166_*170del
ENST00000680582.1:n.1740_1744del
ENST00000680613.1:c.*149_*153del ENSP00000506114.1:n.*149_*153del
ENST00000680662.1:c.*692_*696del ENSP00000505080.1:n.*692_*696del
ENST00000680691.1:c.*441_*445del ENSP00000506487.1:n.*441_*445del
ENST00000680694.1:c.*366_*370del ENSP00000505658.1:n.*366_*370del
ENST00000680743.1:c.*445_*449del ENSP00000505073.1:n.*445_*449del
ENST00000680749.1:c.*63_*67del ENSP00000505122.1:n.*63_*67del
ENST00000680798.1:c.*253_*257del ENSP00000505670.1:n.*253_*257del
ENST00000680805.1:c.709-963_709-959del ENSP00000505447.1:n.709-963_709-959del
ENST00000680844.1:c.*562_*566del ENSP00000506541.1:n.*562_*566del
ENST00000680948.1:c.*645_*649del ENSP00000505441.1:n.*645_*649del
ENST00000680964.1:c.778_782del ENSP00000505961.1:p.Glu260CysfsTer5
ENST00000681037.1:c.*2262_*2266del ENSP00000506025.1:n.*2262_*2266del
ENST00000681063.1:c.600-963_600-959del ENSP00000506616.1:n.600-963_600-959del
ENST00000681209.1:c.*433_*437del ENSP00000505877.1:n.*433_*437del
ENST00000681278.1:n.1135_1139del
ENST00000681289.1:n.4773_4777del
ENST00000681361.1:c.*445_*449del ENSP00000506679.1:n.*445_*449del
ENST00000681430.1:c.778_782del ENSP00000506301.1:p.Glu260CysfsTer5
ENST00000681446.1:c.*360_*364del ENSP00000506244.1:n.*360_*364del
ENST00000681450.1:c.*449_*453del ENSP00000505660.1:n.*449_*453del
ENST00000681548.1:c.*364_*368del ENSP00000505275.1:n.*364_*368del
ENST00000681616.1:c.*437_*441del ENSP00000505111.1:n.*437_*441del
ENST00000681621.1:c.*362_*366del ENSP00000505770.1:n.*362_*366del
ENST00000681680.1:n.2873_2877del
ENST00000681720.1:c.*233_*237del ENSP00000505438.1:n.*233_*237del
ENST00000681730.1:n.1000_1004del
ENST00000681790.1:c.520_524del ENSP00000505130.1:p.Glu174CysfsTer5
ENST00000681837.1:n.1394_1398del
ENST00000681913.1:n.2902_2906del
ENST00000681916.1:c.*546_*550del ENSP00000506477.1:n.*546_*550del
ENST00000681930.1:n.2902_2906del
ENST00000370834.9:c.877_881del ENSP00000359871.5:p.Glu293CysfsTer5
ENST00000370841.8:c.778_782del ENSP00000359878.4:p.Glu260CysfsTer5
ENST00000420607.6:c.790_794del ENSP00000409612.2:p.Glu264CysfsTer5
ENST00000525808.5:c.*364_*368del ENSP00000434823.1:n.*364_*368del
ENST00000526129.5:c.*562_*566del ENSP00000434092.1:n.*562_*566del
ENST00000526196.5:c.*546_*550del ENSP00000431953.1:n.*546_*550del
ENST00000526930.1:n.551_555del
ENST00000529059.5:n.687_691del
ENST00000530953.6:c.*275_*279del ENSP00000431372.1:n.*275_*279del
ENST00000532207.5:n.508_512del
ENST00000532509.5:c.*542_*546del ENSP00000432522.1:n.*542_*546del
ENST00000534334.5:c.*362_*366del ENSP00000435584.1:n.*362_*366del
ENST00000541113.5:c.670_674del ENSP00000442324.1:p.Glu224CysfsTer5
NM_000016.5:c.778_782del NP_000007.1:p.Glu260CysfsTer5
NM_001127328.2:c.790_794del NP_001120800.1:p.Glu264CysfsTer5
NM_001286042.1:c.670_674del NP_001272971.1:p.Glu224CysfsTer5
NM_001286043.1:c.877_881del NP_001272972.1:p.Glu293CysfsTer5
NM_001286044.1:c.211_215del NP_001272973.1:p.Glu71CysfsTer5
NM_000016.6:c.778_782del MANE Select NP_000007.1:p.Glu260CysfsTer5
NM_001127328.3:c.790_794del NP_001120800.1:p.Glu264CysfsTer5
NM_001286042.2:c.670_674del NP_001272971.1:p.Glu224CysfsTer5
NM_001286043.2:c.877_881del NP_001272972.1:p.Glu293CysfsTer5
NM_001286044.2:c.211_215del NP_001272973.1:p.Glu71CysfsTer5