Canonical Allele Identifier: CA2739290467
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345450dup , CM000685.2:g.41345450dup GRCh38
NC_000023.10:g.41204703dup , CM000685.1:g.41204703dup GRCh37
NC_000023.9:g.41089647dup NCBI36
NG_012830.1:g.17053dup
NG_012830.2:g.17053dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1349dup ENSP00000496052.2:p.Arg451LysfsTer7
ENST00000399959.7:c.1214dup ENSP00000382840.3:p.Arg406LysfsTer7
ENST00000441189.4:c.1118dup ENSP00000414281.3:p.Arg374LysfsTer7
ENST00000457138.7:c.1169dup ENSP00000392494.2:p.Arg391LysfsTer7
ENST00000629496.3:c.1217dup ENSP00000487224.1:p.Arg407LysfsTer7
ENST00000642161.1:n.3416dup
ENST00000642322.1:c.659dup ENSP00000496052.1:p.Arg221LysfsTer7
ENST00000642424.1:c.659dup ENSP00000496356.1:p.Arg221LysfsTer7
ENST00000642589.1:n.4539dup
ENST00000642597.1:n.1391dup
ENST00000642687.1:n.1250dup
ENST00000642722.1:n.2050dup
ENST00000642763.1:n.2108dup
ENST00000642793.1:c.*666dup ENSP00000493976.1:n.*666dup
ENST00000642801.1:n.866dup
ENST00000643820.1:n.493dup
ENST00000643963.1:c.*499dup ENSP00000495264.1:n.*499dup
ENST00000644073.1:c.1175dup ENSP00000493475.1:p.Arg393LysfsTer7
ENST00000644074.1:c.1214dup ENSP00000496663.1:p.Arg406LysfsTer7
ENST00000644109.1:c.1379dup ENSP00000494952.1:p.Arg461LysfsTer7
ENST00000644307.1:n.1387dup
ENST00000644513.1:c.1217dup ENSP00000493819.1:p.Arg407LysfsTer7
ENST00000644677.1:c.1100dup ENSP00000496524.1:p.Arg368LysfsTer7
ENST00000644876.2:c.1217dup MANE Select ENSP00000494040.1:p.Arg407LysfsTer7
ENST00000644958.1:n.2878dup
ENST00000645080.1:c.*2439dup ENSP00000494767.1:n.*2439dup
ENST00000645120.1:n.2712dup
ENST00000645338.1:n.1387dup
ENST00000645380.1:n.2681dup
ENST00000645561.1:n.2393dup
ENST00000645574.1:n.4081dup
ENST00000645589.1:c.1217dup ENSP00000494588.1:p.Arg407LysfsTer7
ENST00000646093.1:n.401dup
ENST00000646107.1:c.1100dup ENSP00000494518.1:p.Arg368LysfsTer7
ENST00000646122.1:c.1217dup ENSP00000496222.1:p.Arg407LysfsTer7
ENST00000646196.1:n.2186dup
ENST00000646223.1:c.*1210dup ENSP00000496043.1:n.*1210dup
ENST00000646319.1:c.1217dup ENSP00000495377.1:p.Arg407LysfsTer7
ENST00000646390.1:n.3505dup
ENST00000646627.1:c.659dup ENSP00000493795.1:p.Arg221LysfsTer7
ENST00000646679.1:c.659dup ENSP00000494887.1:p.Arg221LysfsTer7
ENST00000646822.1:n.2279dup
ENST00000646940.1:n.1391dup
ENST00000647286.1:n.1315dup
ENST00000399959.6:c.1217dup ENSP00000382840.2:p.Arg407LysfsTer7
ENST00000441189.3:c.341-2190dup ENSP00000414281.2:n.341-2190dup
ENST00000457138.6:c.1169dup ENSP00000392494.2:p.Arg391LysfsTer7
ENST00000478993.5:c.1217dup ENSP00000478443.1:p.Arg407LysfsTer7
ENST00000542215.5:n.1265dup
ENST00000625837.2:c.1217dup ENSP00000486306.1:p.Arg407LysfsTer7
ENST00000626301.2:c.1217dup ENSP00000486443.1:p.Arg407LysfsTer7
ENST00000629496.2:c.1217dup ENSP00000487224.1:p.Arg407LysfsTer7
ENST00000629785.2:c.1217dup ENSP00000486516.1:p.Arg407LysfsTer7
ENST00000630255.2:c.1217dup ENSP00000486720.1:p.Arg407LysfsTer7
ENST00000630370.2:c.1217dup ENSP00000487062.1:p.Arg407LysfsTer7
ENST00000630858.2:c.1217dup ENSP00000486514.1:p.Arg407LysfsTer7
NM_001193416.2:c.1217dup NP_001180345.1:p.Arg407LysfsTer7
NM_001193417.2:c.1169dup NP_001180346.1:p.Arg391LysfsTer7
NM_001356.4:c.1217dup NP_001347.3:p.Arg407LysfsTer7
NR_126093.1:n.2162dup
XM_011543892.1:c.1217dup XP_011542194.1:p.Arg407LysfsTer7
NM_001363819.1:c.659dup NP_001350748.1:p.Arg221LysfsTer7
XM_011543892.2:c.1217dup XP_011542194.1:p.Arg407LysfsTer7
XM_017029313.1:c.659dup XP_016884802.1:p.Arg221LysfsTer7
NM_001193416.3:c.1217dup NP_001180345.1:p.Arg407LysfsTer7
NM_001193417.3:c.1169dup NP_001180346.1:p.Arg391LysfsTer7
NM_001356.5:c.1217dup MANE Select NP_001347.3:p.Arg407LysfsTer7