Canonical Allele Identifier: CA875368037
Gene: DDX3X HGNC NCBI

Linked Data

dbSNP Id: rs774166436

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345388del , CM000685.2:g.41345388del GRCh38
NC_000023.10:g.41204641del , CM000685.1:g.41204641del GRCh37
NC_000023.9:g.41089585del NCBI36
NG_012830.1:g.16991del
NG_012830.2:g.16991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1303-16del ENSP00000496052.2:n.1303-16del
ENST00000399959.7:c.1168-16del ENSP00000382840.3:n.1168-16del
ENST00000441189.4:c.1072-16del ENSP00000414281.3:n.1072-16del
ENST00000457138.7:c.1123-16del ENSP00000392494.2:n.1123-16del
ENST00000629496.3:c.1171-16del ENSP00000487224.1:n.1171-16del
ENST00000642161.1:n.3370-16del
ENST00000642322.1:c.613-16del ENSP00000496052.1:n.613-16del
ENST00000642424.1:c.613-16del ENSP00000496356.1:n.613-16del
ENST00000642589.1:n.4493-16del
ENST00000642597.1:n.1345-16del
ENST00000642687.1:n.1204-16del
ENST00000642722.1:n.2004-16del
ENST00000642763.1:n.2062-16del
ENST00000642793.1:c.*620-16del ENSP00000493976.1:n.*620-16del
ENST00000642801.1:n.820-16del
ENST00000643820.1:n.447-16del
ENST00000643963.1:c.*453-16del ENSP00000495264.1:n.*453-16del
ENST00000644073.1:c.1129-16del ENSP00000493475.1:n.1129-16del
ENST00000644074.1:c.1168-16del ENSP00000496663.1:n.1168-16del
ENST00000644109.1:c.1333-16del ENSP00000494952.1:n.1333-16del
ENST00000644307.1:n.1325del
ENST00000644513.1:c.1171-16del ENSP00000493819.1:n.1171-16del
ENST00000644677.1:c.1054-16del ENSP00000496524.1:n.1054-16del
ENST00000644876.2:c.1171-16del MANE Select ENSP00000494040.1:n.1171-16del
ENST00000644958.1:n.2832-16del
ENST00000645080.1:c.*2393-16del ENSP00000494767.1:n.*2393-16del
ENST00000645120.1:n.2666-16del
ENST00000645338.1:n.1325del
ENST00000645380.1:n.2619del
ENST00000645561.1:n.2347-16del
ENST00000645574.1:n.4035-16del
ENST00000645589.1:c.1171-16del ENSP00000494588.1:n.1171-16del
ENST00000646093.1:n.355-16del
ENST00000646107.1:c.1054-16del ENSP00000494518.1:n.1054-16del
ENST00000646122.1:c.1171-16del ENSP00000496222.1:n.1171-16del
ENST00000646196.1:n.2140-16del
ENST00000646223.1:c.*1164-16del ENSP00000496043.1:n.*1164-16del
ENST00000646319.1:c.1171-16del ENSP00000495377.1:n.1171-16del
ENST00000646390.1:n.3459-16del
ENST00000646627.1:c.613-16del ENSP00000493795.1:n.613-16del
ENST00000646679.1:c.613-16del ENSP00000494887.1:n.613-16del
ENST00000646822.1:n.2233-16del
ENST00000646940.1:n.1345-16del
ENST00000647286.1:n.1269-16del
ENST00000399959.6:c.1171-16del ENSP00000382840.2:n.1171-16del
ENST00000441189.3:c.341-2252del ENSP00000414281.2:n.341-2252del
ENST00000457138.6:c.1123-16del ENSP00000392494.2:n.1123-16del
ENST00000478993.5:c.1171-16del ENSP00000478443.1:n.1171-16del
ENST00000542215.5:n.1219-16del
ENST00000625837.2:c.1171-16del ENSP00000486306.1:n.1171-16del
ENST00000626301.2:c.1171-16del ENSP00000486443.1:n.1171-16del
ENST00000629496.2:c.1171-16del ENSP00000487224.1:n.1171-16del
ENST00000629785.2:c.1171-16del ENSP00000486516.1:n.1171-16del
ENST00000630255.2:c.1171-16del ENSP00000486720.1:n.1171-16del
ENST00000630370.2:c.1171-16del ENSP00000487062.1:n.1171-16del
ENST00000630858.2:c.1171-16del ENSP00000486514.1:n.1171-16del
NM_001193416.2:c.1171-16del NP_001180345.1:n.1171-16del
NM_001193417.2:c.1123-16del NP_001180346.1:n.1123-16del
NM_001356.4:c.1171-16del NP_001347.3:n.1171-16del
NR_126093.1:n.2116-16del
XM_011543892.1:c.1171-16del XP_011542194.1:n.1171-16del
NM_001363819.1:c.613-16del NP_001350748.1:n.613-16del
XM_011543892.2:c.1171-16del XP_011542194.1:n.1171-16del
XM_017029313.1:c.613-16del XP_016884802.1:n.613-16del
NM_001193416.3:c.1171-16del NP_001180345.1:n.1171-16del
NM_001193417.3:c.1123-16del NP_001180346.1:n.1123-16del
NM_001356.5:c.1171-16del MANE Select NP_001347.3:n.1171-16del