Canonical Allele Identifier: CA2569405095
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749449_75749450insTCAT , CM000663.2:g.75749449_75749450insTCAT GRCh38
NC_000001.10:g.76215134_76215135insTCAT , CM000663.1:g.76215134_76215135insTCAT GRCh37
NC_000001.9:g.75987722_75987723insTCAT NCBI36
NG_007045.2:g.30092_30093insTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.739_740insTCAT MANE Select ENSP00000359878.5:p.Thr247IlefsTer3
ENST00000473018.3:n.2863_2864insTCAT
ENST00000532207.6:n.1628_1629insTCAT
ENST00000541113.6:c.739_740insTCAT ENSP00000442324.2:p.Thr247IlefsTer3
ENST00000679509.1:n.1701_1702insTCAT
ENST00000679530.1:c.*507_*508insTCAT ENSP00000506454.1:n.*507_*508insTCAT
ENST00000679615.1:n.2754_2755insTCAT
ENST00000679687.1:c.301_302insTCAT ENSP00000506598.1:p.Thr101IlefsTer3
ENST00000679704.1:c.*505_*506insTCAT ENSP00000505117.1:n.*505_*506insTCAT
ENST00000679709.1:c.*702_*703insTCAT ENSP00000506623.1:n.*702_*703insTCAT
ENST00000679976.1:c.*323_*324insTCAT ENSP00000505565.1:n.*323_*324insTCAT
ENST00000680166.1:n.4028_4029insTCAT
ENST00000680517.1:c.*127_*128insTCAT ENSP00000505803.1:n.*127_*128insTCAT
ENST00000680582.1:n.1701_1702insTCAT
ENST00000680613.1:c.*110_*111insTCAT ENSP00000506114.1:n.*110_*111insTCAT
ENST00000680662.1:c.*653_*654insTCAT ENSP00000505080.1:n.*653_*654insTCAT
ENST00000680691.1:c.*402_*403insTCAT ENSP00000506487.1:n.*402_*403insTCAT
ENST00000680694.1:c.*327_*328insTCAT ENSP00000505658.1:n.*327_*328insTCAT
ENST00000680743.1:c.*406_*407insTCAT ENSP00000505073.1:n.*406_*407insTCAT
ENST00000680749.1:c.*24_*25insTCAT ENSP00000505122.1:n.*24_*25insTCAT
ENST00000680798.1:c.*214_*215insTCAT ENSP00000505670.1:n.*214_*215insTCAT
ENST00000680805.1:c.709-1002_709-1001insTCAT ENSP00000505447.1:n.709-1002_709-1001insTCAT
ENST00000680844.1:c.*523_*524insTCAT ENSP00000506541.1:n.*523_*524insTCAT
ENST00000680948.1:c.*606_*607insTCAT ENSP00000505441.1:n.*606_*607insTCAT
ENST00000680964.1:c.739_740insTCAT ENSP00000505961.1:p.Thr247IlefsTer3
ENST00000681037.1:c.*2223_*2224insTCAT ENSP00000506025.1:n.*2223_*2224insTCAT
ENST00000681063.1:c.600-1002_600-1001insTCAT ENSP00000506616.1:n.600-1002_600-1001insTCAT
ENST00000681209.1:c.*394_*395insTCAT ENSP00000505877.1:n.*394_*395insTCAT
ENST00000681278.1:n.1096_1097insTCAT
ENST00000681289.1:n.4734_4735insTCAT
ENST00000681361.1:c.*406_*407insTCAT ENSP00000506679.1:n.*406_*407insTCAT
ENST00000681430.1:c.739_740insTCAT ENSP00000506301.1:p.Thr247IlefsTer3
ENST00000681446.1:c.*321_*322insTCAT ENSP00000506244.1:n.*321_*322insTCAT
ENST00000681450.1:c.*410_*411insTCAT ENSP00000505660.1:n.*410_*411insTCAT
ENST00000681548.1:c.*325_*326insTCAT ENSP00000505275.1:n.*325_*326insTCAT
ENST00000681616.1:c.*398_*399insTCAT ENSP00000505111.1:n.*398_*399insTCAT
ENST00000681621.1:c.*323_*324insTCAT ENSP00000505770.1:n.*323_*324insTCAT
ENST00000681680.1:n.2834_2835insTCAT
ENST00000681720.1:c.*194_*195insTCAT ENSP00000505438.1:n.*194_*195insTCAT
ENST00000681730.1:n.961_962insTCAT
ENST00000681790.1:c.481_482insTCAT ENSP00000505130.1:p.Thr161IlefsTer3
ENST00000681837.1:n.1355_1356insTCAT
ENST00000681913.1:n.2863_2864insTCAT
ENST00000681916.1:c.*507_*508insTCAT ENSP00000506477.1:n.*507_*508insTCAT
ENST00000681930.1:n.2863_2864insTCAT
ENST00000370834.9:c.838_839insTCAT ENSP00000359871.5:p.Thr280IlefsTer3
ENST00000370841.8:c.739_740insTCAT ENSP00000359878.4:p.Thr247IlefsTer3
ENST00000420607.6:c.751_752insTCAT ENSP00000409612.2:p.Thr251IlefsTer3
ENST00000525808.5:c.*325_*326insTCAT ENSP00000434823.1:n.*325_*326insTCAT
ENST00000526129.5:c.*523_*524insTCAT ENSP00000434092.1:n.*523_*524insTCAT
ENST00000526196.5:c.*507_*508insTCAT ENSP00000431953.1:n.*507_*508insTCAT
ENST00000526930.1:n.512_513insTCAT
ENST00000529059.5:n.648_649insTCAT
ENST00000530953.6:c.*236_*237insTCAT ENSP00000431372.1:n.*236_*237insTCAT
ENST00000532207.5:n.469_470insTCAT
ENST00000532509.5:c.*503_*504insTCAT ENSP00000432522.1:n.*503_*504insTCAT
ENST00000534334.5:c.*323_*324insTCAT ENSP00000435584.1:n.*323_*324insTCAT
ENST00000541113.5:c.631_632insTCAT ENSP00000442324.1:p.Thr211IlefsTer3
NM_000016.5:c.739_740insTCAT NP_000007.1:p.Thr247IlefsTer3
NM_001127328.2:c.751_752insTCAT NP_001120800.1:p.Thr251IlefsTer3
NM_001286042.1:c.631_632insTCAT NP_001272971.1:p.Thr211IlefsTer3
NM_001286043.1:c.838_839insTCAT NP_001272972.1:p.Thr280IlefsTer3
NM_001286044.1:c.172_173insTCAT NP_001272973.1:p.Thr58IlefsTer3
NM_000016.6:c.739_740insTCAT MANE Select NP_000007.1:p.Thr247IlefsTer3
NM_001127328.3:c.751_752insTCAT NP_001120800.1:p.Thr251IlefsTer3
NM_001286042.2:c.631_632insTCAT NP_001272971.1:p.Thr211IlefsTer3
NM_001286043.2:c.838_839insTCAT NP_001272972.1:p.Thr280IlefsTer3
NM_001286044.2:c.172_173insTCAT NP_001272973.1:p.Thr58IlefsTer3