Canonical Allele Identifier: CA3051372168
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749450_75749452dup , CM000663.2:g.75749450_75749452dup GRCh38
NC_000001.10:g.76215135_76215137dup , CM000663.1:g.76215135_76215137dup GRCh37
NC_000001.9:g.75987723_75987725dup NCBI36
NG_007045.2:g.30093_30095dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.740_742dup MANE Select ENSP00000359878.5:p.Thr247_Arg248insThr
ENST00000473018.3:n.2864_2866dup
ENST00000532207.6:n.1629_1631dup
ENST00000541113.6:c.740_742dup ENSP00000442324.2:p.Thr247_Arg248insThr
ENST00000679509.1:n.1702_1704dup
ENST00000679530.1:c.*508_*510dup ENSP00000506454.1:n.*508_*510dup
ENST00000679615.1:n.2755_2757dup
ENST00000679687.1:c.302_304dup ENSP00000506598.1:p.Thr101_Arg102insThr
ENST00000679704.1:c.*506_*508dup ENSP00000505117.1:n.*506_*508dup
ENST00000679709.1:c.*703_*705dup ENSP00000506623.1:n.*703_*705dup
ENST00000679976.1:c.*324_*326dup ENSP00000505565.1:n.*324_*326dup
ENST00000680166.1:n.4029_4031dup
ENST00000680517.1:c.*128_*130dup ENSP00000505803.1:n.*128_*130dup
ENST00000680582.1:n.1702_1704dup
ENST00000680613.1:c.*111_*113dup ENSP00000506114.1:n.*111_*113dup
ENST00000680662.1:c.*654_*656dup ENSP00000505080.1:n.*654_*656dup
ENST00000680691.1:c.*403_*405dup ENSP00000506487.1:n.*403_*405dup
ENST00000680694.1:c.*328_*330dup ENSP00000505658.1:n.*328_*330dup
ENST00000680743.1:c.*407_*409dup ENSP00000505073.1:n.*407_*409dup
ENST00000680749.1:c.*25_*27dup ENSP00000505122.1:n.*25_*27dup
ENST00000680798.1:c.*215_*217dup ENSP00000505670.1:n.*215_*217dup
ENST00000680805.1:c.709-1001_709-999dup ENSP00000505447.1:n.709-1001_709-999dup
ENST00000680844.1:c.*524_*526dup ENSP00000506541.1:n.*524_*526dup
ENST00000680948.1:c.*607_*609dup ENSP00000505441.1:n.*607_*609dup
ENST00000680964.1:c.740_742dup ENSP00000505961.1:p.Thr247_Arg248insThr
ENST00000681037.1:c.*2224_*2226dup ENSP00000506025.1:n.*2224_*2226dup
ENST00000681063.1:c.600-1001_600-999dup ENSP00000506616.1:n.600-1001_600-999dup
ENST00000681209.1:c.*395_*397dup ENSP00000505877.1:n.*395_*397dup
ENST00000681278.1:n.1097_1099dup
ENST00000681289.1:n.4735_4737dup
ENST00000681361.1:c.*407_*409dup ENSP00000506679.1:n.*407_*409dup
ENST00000681430.1:c.740_742dup ENSP00000506301.1:p.Thr247_Arg248insThr
ENST00000681446.1:c.*322_*324dup ENSP00000506244.1:n.*322_*324dup
ENST00000681450.1:c.*411_*413dup ENSP00000505660.1:n.*411_*413dup
ENST00000681548.1:c.*326_*328dup ENSP00000505275.1:n.*326_*328dup
ENST00000681616.1:c.*399_*401dup ENSP00000505111.1:n.*399_*401dup
ENST00000681621.1:c.*324_*326dup ENSP00000505770.1:n.*324_*326dup
ENST00000681680.1:n.2835_2837dup
ENST00000681720.1:c.*195_*197dup ENSP00000505438.1:n.*195_*197dup
ENST00000681730.1:n.962_964dup
ENST00000681790.1:c.482_484dup ENSP00000505130.1:p.Thr161_Arg162insThr
ENST00000681837.1:n.1356_1358dup
ENST00000681913.1:n.2864_2866dup
ENST00000681916.1:c.*508_*510dup ENSP00000506477.1:n.*508_*510dup
ENST00000681930.1:n.2864_2866dup
ENST00000370834.9:c.839_841dup ENSP00000359871.5:p.Thr280_Arg281insThr
ENST00000370841.8:c.740_742dup ENSP00000359878.4:p.Thr247_Arg248insThr
ENST00000420607.6:c.752_754dup ENSP00000409612.2:p.Thr251_Arg252insThr
ENST00000525808.5:c.*326_*328dup ENSP00000434823.1:n.*326_*328dup
ENST00000526129.5:c.*524_*526dup ENSP00000434092.1:n.*524_*526dup
ENST00000526196.5:c.*508_*510dup ENSP00000431953.1:n.*508_*510dup
ENST00000526930.1:n.513_515dup
ENST00000529059.5:n.649_651dup
ENST00000530953.6:c.*237_*239dup ENSP00000431372.1:n.*237_*239dup
ENST00000532207.5:n.470_472dup
ENST00000532509.5:c.*504_*506dup ENSP00000432522.1:n.*504_*506dup
ENST00000534334.5:c.*324_*326dup ENSP00000435584.1:n.*324_*326dup
ENST00000541113.5:c.632_634dup ENSP00000442324.1:p.Thr211_Arg212insThr
NM_000016.5:c.740_742dup NP_000007.1:p.Thr247_Arg248insThr
NM_001127328.2:c.752_754dup NP_001120800.1:p.Thr251_Arg252insThr
NM_001286042.1:c.632_634dup NP_001272971.1:p.Thr211_Arg212insThr
NM_001286043.1:c.839_841dup NP_001272972.1:p.Thr280_Arg281insThr
NM_001286044.1:c.173_175dup NP_001272973.1:p.Thr58_Arg59insThr
NM_000016.6:c.740_742dup MANE Select NP_000007.1:p.Thr247_Arg248insThr
NM_001127328.3:c.752_754dup NP_001120800.1:p.Thr251_Arg252insThr
NM_001286042.2:c.632_634dup NP_001272971.1:p.Thr211_Arg212insThr
NM_001286043.2:c.839_841dup NP_001272972.1:p.Thr280_Arg281insThr
NM_001286044.2:c.173_175dup NP_001272973.1:p.Thr58_Arg59insThr