Canonical Allele Identifier: CA2579588537
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346300del , CM000685.2:g.41346300del GRCh38
NC_000023.10:g.41205553del , CM000685.1:g.41205553del GRCh37
NC_000023.9:g.41090497del NCBI36
NG_012830.1:g.17903del
NG_012830.2:g.17903del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1519del ENSP00000496052.2:p.His507MetfsTer?
ENST00000399959.7:c.1384del ENSP00000382840.3:p.His462MetfsTer?
ENST00000441189.4:c.1288del ENSP00000414281.3:p.His430MetfsTer?
ENST00000457138.7:c.1339del ENSP00000392494.2:p.His447MetfsTer?
ENST00000616050.3:c.135del
ENST00000629496.3:c.1387del ENSP00000487224.1:p.His463MetfsTer?
ENST00000642161.1:n.3586del
ENST00000642322.1:c.829del ENSP00000496052.1:p.His277MetfsTer?
ENST00000642424.1:c.829del ENSP00000496356.1:p.His277MetfsTer?
ENST00000642589.1:n.4709del
ENST00000642597.1:n.1561del
ENST00000642687.1:n.1420del
ENST00000642722.1:n.2220del
ENST00000642763.1:n.2278del
ENST00000642793.1:c.*836del ENSP00000493976.1:n.*836del
ENST00000642801.1:n.1036del
ENST00000643820.1:n.663del
ENST00000643963.1:c.*669del ENSP00000495264.1:n.*669del
ENST00000644073.1:c.1345del ENSP00000493475.1:p.His449MetfsTer?
ENST00000644074.1:c.1384del ENSP00000496663.1:p.His462MetfsTer?
ENST00000644109.1:c.1549del ENSP00000494952.1:p.His517MetfsTer?
ENST00000644307.1:n.1557del
ENST00000644513.1:c.1387del ENSP00000493819.1:p.His463MetfsTer?
ENST00000644677.1:c.1270del ENSP00000496524.1:p.His424MetfsTer?
ENST00000644876.2:c.1387del MANE Select ENSP00000494040.1:p.His463MetfsTer?
ENST00000644958.1:n.3048del
ENST00000645080.1:c.*2609del ENSP00000494767.1:n.*2609del
ENST00000645120.1:n.2882del
ENST00000645338.1:n.1557del
ENST00000645380.1:n.2851del
ENST00000645561.1:n.2563del
ENST00000645574.1:n.4251del
ENST00000645589.1:c.1387del ENSP00000494588.1:p.His463MetfsTer?
ENST00000646107.1:c.1270del ENSP00000494518.1:p.His424MetfsTer?
ENST00000646122.1:c.1387del ENSP00000496222.1:p.His463MetfsTer?
ENST00000646196.1:n.2356del
ENST00000646223.1:c.*1380del ENSP00000496043.1:n.*1380del
ENST00000646319.1:c.1387del ENSP00000495377.1:p.His463MetfsTer?
ENST00000646390.1:n.3675del
ENST00000646627.1:c.829del ENSP00000493795.1:p.His277MetfsTer?
ENST00000646679.1:c.829del ENSP00000494887.1:p.His277MetfsTer?
ENST00000646822.1:n.2449del
ENST00000646940.1:n.1561del
ENST00000647286.1:n.1485del
ENST00000647477.1:n.126del
ENST00000399959.6:c.1387del ENSP00000382840.2:p.His463MetfsTer?
ENST00000441189.3:c.341-1340del ENSP00000414281.2:n.341-1340del
ENST00000457138.6:c.1339del ENSP00000392494.2:p.His447MetfsTer?
ENST00000478993.5:c.1387del ENSP00000478443.1:p.His463MetfsTer?
ENST00000542215.5:n.1435del
ENST00000625837.2:c.1387del ENSP00000486306.1:p.His463MetfsTer?
ENST00000626301.2:c.1387del ENSP00000486443.1:p.His463MetfsTer?
ENST00000629496.2:c.1387del ENSP00000487224.1:p.His463MetfsTer?
ENST00000629785.2:c.1387del ENSP00000486516.1:p.His463MetfsTer?
ENST00000630255.2:c.1387del ENSP00000486720.1:p.His463MetfsTer?
ENST00000630370.2:c.1387del ENSP00000487062.1:p.His463MetfsTer?
ENST00000630858.2:c.1387del ENSP00000486514.1:p.His463MetfsTer?
NM_001193416.2:c.1387del NP_001180345.1:p.His463MetfsTer?
NM_001193417.2:c.1339del NP_001180346.1:p.His447MetfsTer?
NM_001356.4:c.1387del NP_001347.3:p.His463MetfsTer?
NR_126093.1:n.2332del
XM_011543892.1:c.1387del XP_011542194.1:p.His463MetfsTer?
NM_001363819.1:c.829del NP_001350748.1:p.His277MetfsTer?
XM_011543892.2:c.1387del XP_011542194.1:p.His463MetfsTer?
XM_017029313.1:c.829del XP_016884802.1:p.His277MetfsTer?
NM_001193416.3:c.1387del NP_001180345.1:p.His463MetfsTer?
NM_001193417.3:c.1339del NP_001180346.1:p.His447MetfsTer?
NM_001356.5:c.1387del MANE Select NP_001347.3:p.His463MetfsTer?