Canonical Allele Identifier: CA24627600
Gene: ACADM HGNC NCBI

Linked Data

dbSNP Id: rs35922788

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75739997dup , CM000663.2:g.75739997dup GRCh38
NC_000001.10:g.76205682dup , CM000663.1:g.76205682dup GRCh37
NC_000001.9:g.75978270dup NCBI36
NG_007045.2:g.20640dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.486dup MANE Select ENSP00000359878.5:p.Pro163ThrfsTer6
ENST00000473018.3:n.2610dup
ENST00000541113.6:c.486dup ENSP00000442324.2:p.Pro163ThrfsTer6
ENST00000679509.1:n.1448dup
ENST00000679530.1:c.*254dup ENSP00000506454.1:n.*254dup
ENST00000679615.1:n.2610dup
ENST00000679687.1:c.48dup ENSP00000506598.1:p.Pro17ThrfsTer6
ENST00000679704.1:c.*252dup ENSP00000505117.1:n.*252dup
ENST00000679709.1:c.*449dup ENSP00000506623.1:n.*449dup
ENST00000679804.1:n.225dup
ENST00000679976.1:c.*70dup ENSP00000505565.1:n.*70dup
ENST00000680166.1:n.3775dup
ENST00000680517.1:c.304dup ENSP00000505803.1:p.Thr102AsnfsTer8
ENST00000680582.1:n.1448dup
ENST00000680613.1:c.486dup ENSP00000506114.1:p.Pro163ThrfsTer6
ENST00000680662.1:c.*400dup ENSP00000505080.1:n.*400dup
ENST00000680691.1:c.*149dup ENSP00000506487.1:n.*149dup
ENST00000680694.1:c.*74dup ENSP00000505658.1:n.*74dup
ENST00000680743.1:c.*153dup ENSP00000505073.1:n.*153dup
ENST00000680749.1:c.486dup ENSP00000505122.1:p.Pro163ThrfsTer6
ENST00000680798.1:c.*70dup ENSP00000505670.1:n.*70dup
ENST00000680805.1:c.486dup ENSP00000505447.1:p.Pro163ThrfsTer6
ENST00000680844.1:c.*270dup ENSP00000506541.1:n.*270dup
ENST00000680948.1:c.*353dup ENSP00000505441.1:n.*353dup
ENST00000680964.1:c.486dup ENSP00000505961.1:p.Pro163ThrfsTer6
ENST00000681037.1:c.486dup ENSP00000506025.1:p.Pro163ThrfsTer6
ENST00000681063.1:c.486dup ENSP00000506616.1:p.Pro163ThrfsTer6
ENST00000681209.1:c.*250dup ENSP00000505877.1:n.*250dup
ENST00000681278.1:n.843dup
ENST00000681289.1:n.843dup
ENST00000681361.1:c.*153dup ENSP00000506679.1:n.*153dup
ENST00000681430.1:c.486dup ENSP00000506301.1:p.Pro163ThrfsTer6
ENST00000681446.1:c.*68dup ENSP00000506244.1:n.*68dup
ENST00000681450.1:c.*157dup ENSP00000505660.1:n.*157dup
ENST00000681548.1:c.*72dup ENSP00000505275.1:n.*72dup
ENST00000681616.1:c.*254dup ENSP00000505111.1:n.*254dup
ENST00000681621.1:c.*70dup ENSP00000505770.1:n.*70dup
ENST00000681680.1:n.2610dup
ENST00000681720.1:c.*55-5809dup ENSP00000505438.1:n.*55-5809dup
ENST00000681730.1:n.708dup
ENST00000681790.1:c.228dup ENSP00000505130.1:p.Pro77ThrfsTer6
ENST00000681837.1:n.1102dup
ENST00000681913.1:n.2610dup
ENST00000681916.1:c.*254dup ENSP00000506477.1:n.*254dup
ENST00000681930.1:n.2610dup
ENST00000370834.9:c.585dup ENSP00000359871.5:p.Pro196ThrfsTer6
ENST00000370841.8:c.486dup ENSP00000359878.4:p.Pro163ThrfsTer6
ENST00000420607.6:c.498dup ENSP00000409612.2:p.Pro167ThrfsTer6
ENST00000525808.5:c.*72dup ENSP00000434823.1:n.*72dup
ENST00000526129.5:c.*270dup ENSP00000434092.1:n.*270dup
ENST00000526196.5:c.*254dup ENSP00000431953.1:n.*254dup
ENST00000526930.1:n.259dup
ENST00000529059.5:n.395dup
ENST00000530953.6:c.136dup ENSP00000431372.1:p.Thr46AsnfsTer8
ENST00000532509.5:c.*250dup ENSP00000432522.1:n.*250dup
ENST00000534334.5:c.*70dup ENSP00000435584.1:n.*70dup
ENST00000541113.5:c.378dup ENSP00000442324.1:p.Pro127ThrfsTer6
NM_000016.5:c.486dup NP_000007.1:p.Pro163ThrfsTer6
NM_001127328.2:c.498dup NP_001120800.1:p.Pro167ThrfsTer6
NM_001286042.1:c.378dup NP_001272971.1:p.Pro127ThrfsTer6
NM_001286043.1:c.585dup NP_001272972.1:p.Pro196ThrfsTer6
NM_001286044.1:c.-82dup NP_001272973.1:n.-82dup
NM_000016.6:c.486dup MANE Select NP_000007.1:p.Pro163ThrfsTer6
NM_001127328.3:c.498dup NP_001120800.1:p.Pro167ThrfsTer6
NM_001286042.2:c.378dup NP_001272971.1:p.Pro127ThrfsTer6
NM_001286043.2:c.585dup NP_001272972.1:p.Pro196ThrfsTer6
NM_001286044.2:c.-82dup NP_001272973.1:n.-82dup