Canonical Allele Identifier: CA2499214855
Gene: ACADM HGNC NCBI

Linked Data

ClinVar Variation Id: 1070356
ClinVar RCV Id: RCV001382469
dbSNP Id: rs2100417735

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749509_75749513del , CM000663.2:g.75749509_75749513del GRCh38
NC_000001.10:g.76215194_76215198del , CM000663.1:g.76215194_76215198del GRCh37
NC_000001.9:g.75987782_75987786del NCBI36
NG_007045.2:g.30152_30156del

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.799_803del MANE Select ENSP00000359878.5:p.Gly267TrpfsTer10
ENST00000473018.3:n.2923_2927del
ENST00000532207.6:n.1688_1692del
ENST00000541113.6:c.799_803del ENSP00000442324.2:p.Gly267TrpfsTer10
ENST00000679509.1:n.1761_1765del
ENST00000679530.1:c.*567_*571del ENSP00000506454.1:n.*567_*571del
ENST00000679615.1:n.2814_2818del
ENST00000679687.1:c.361_365del ENSP00000506598.1:p.Gly121TrpfsTer10
ENST00000679704.1:c.*565_*569del ENSP00000505117.1:n.*565_*569del
ENST00000679709.1:c.*762_*766del ENSP00000506623.1:n.*762_*766del
ENST00000679976.1:c.*383_*387del ENSP00000505565.1:n.*383_*387del
ENST00000680166.1:n.4088_4092del
ENST00000680517.1:c.*187_*191del ENSP00000505803.1:n.*187_*191del
ENST00000680582.1:n.1761_1765del
ENST00000680613.1:c.*170_*174del ENSP00000506114.1:n.*170_*174del
ENST00000680662.1:c.*713_*717del ENSP00000505080.1:n.*713_*717del
ENST00000680691.1:c.*462_*466del ENSP00000506487.1:n.*462_*466del
ENST00000680694.1:c.*387_*391del ENSP00000505658.1:n.*387_*391del
ENST00000680743.1:c.*466_*470del ENSP00000505073.1:n.*466_*470del
ENST00000680749.1:c.*84_*88del ENSP00000505122.1:n.*84_*88del
ENST00000680798.1:c.*274_*278del ENSP00000505670.1:n.*274_*278del
ENST00000680805.1:c.709-942_709-938del ENSP00000505447.1:n.709-942_709-938del
ENST00000680844.1:c.*583_*587del ENSP00000506541.1:n.*583_*587del
ENST00000680948.1:c.*666_*670del ENSP00000505441.1:n.*666_*670del
ENST00000680964.1:c.799_803del ENSP00000505961.1:p.Gly267TrpfsTer10
ENST00000681037.1:c.*2283_*2287del ENSP00000506025.1:n.*2283_*2287del
ENST00000681063.1:c.600-942_600-938del ENSP00000506616.1:n.600-942_600-938del
ENST00000681209.1:c.*454_*458del ENSP00000505877.1:n.*454_*458del
ENST00000681278.1:n.1156_1160del
ENST00000681289.1:n.4794_4798del
ENST00000681361.1:c.*466_*470del ENSP00000506679.1:n.*466_*470del
ENST00000681430.1:c.799_803del ENSP00000506301.1:p.Gly267TrpfsTer10
ENST00000681446.1:c.*381_*385del ENSP00000506244.1:n.*381_*385del
ENST00000681450.1:c.*470_*474del ENSP00000505660.1:n.*470_*474del
ENST00000681548.1:c.*385_*389del ENSP00000505275.1:n.*385_*389del
ENST00000681616.1:c.*458_*462del ENSP00000505111.1:n.*458_*462del
ENST00000681621.1:c.*383_*387del ENSP00000505770.1:n.*383_*387del
ENST00000681680.1:n.2894_2898del
ENST00000681720.1:c.*254_*258del ENSP00000505438.1:n.*254_*258del
ENST00000681730.1:n.1021_1025del
ENST00000681790.1:c.541_545del ENSP00000505130.1:p.Gly181TrpfsTer10
ENST00000681837.1:n.1415_1419del
ENST00000681913.1:n.2923_2927del
ENST00000681916.1:c.*567_*571del ENSP00000506477.1:n.*567_*571del
ENST00000681930.1:n.2923_2927del
ENST00000370834.9:c.898_902del ENSP00000359871.5:p.Gly300TrpfsTer10
ENST00000370841.8:c.799_803del ENSP00000359878.4:p.Gly267TrpfsTer10
ENST00000420607.6:c.811_815del ENSP00000409612.2:p.Gly271TrpfsTer10
ENST00000525808.5:c.*385_*389del ENSP00000434823.1:n.*385_*389del
ENST00000526129.5:c.*583_*587del ENSP00000434092.1:n.*583_*587del
ENST00000526196.5:c.*567_*571del ENSP00000431953.1:n.*567_*571del
ENST00000526930.1:n.572_576del
ENST00000528016.1:c.13_17del ENSP00000434284.1:p.Gly5TrpfsTer10
ENST00000529059.5:n.708_712del
ENST00000530953.6:c.*296_*300del ENSP00000431372.1:n.*296_*300del
ENST00000532207.5:n.529_533del
ENST00000532509.5:c.*563_*567del ENSP00000432522.1:n.*563_*567del
ENST00000534334.5:c.*383_*387del ENSP00000435584.1:n.*383_*387del
ENST00000541113.5:c.691_695del ENSP00000442324.1:p.Gly231TrpfsTer10
NM_000016.5:c.799_803del NP_000007.1:p.Gly267TrpfsTer10
NM_001127328.2:c.811_815del NP_001120800.1:p.Gly271TrpfsTer10
NM_001286042.1:c.691_695del NP_001272971.1:p.Gly231TrpfsTer10
NM_001286043.1:c.898_902del NP_001272972.1:p.Gly300TrpfsTer10
NM_001286044.1:c.232_236del NP_001272973.1:p.Gly78TrpfsTer10
NM_000016.6:c.799_803del MANE Select NP_000007.1:p.Gly267TrpfsTer10
NM_001127328.3:c.811_815del NP_001120800.1:p.Gly271TrpfsTer10
NM_001286042.2:c.691_695del NP_001272971.1:p.Gly231TrpfsTer10
NM_001286043.2:c.898_902del NP_001272972.1:p.Gly300TrpfsTer10
NM_001286044.2:c.232_236del NP_001272973.1:p.Gly78TrpfsTer10