Canonical Allele Identifier: CA2837995236
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41344267dup , CM000685.2:g.41344267dup GRCh38
NC_000023.10:g.41203520dup , CM000685.1:g.41203520dup GRCh37
NC_000023.9:g.41088464dup NCBI36
NG_012830.1:g.15870dup
NG_012830.2:g.15870dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1025dup ENSP00000496052.2:p.Cys342TrpfsTer?
ENST00000399959.7:c.890dup ENSP00000382840.3:p.Cys297TrpfsTer?
ENST00000441189.4:c.794dup ENSP00000414281.3:p.Cys265TrpfsTer?
ENST00000457138.7:c.845dup ENSP00000392494.2:p.Cys282TrpfsTer?
ENST00000629496.3:c.893dup ENSP00000487224.1:p.Cys298TrpfsTer?
ENST00000631641.2:n.936dup
ENST00000642161.1:n.3092dup
ENST00000642322.1:c.335dup ENSP00000496052.1:p.Cys112TrpfsTer?
ENST00000642424.1:c.335dup ENSP00000496356.1:p.Cys112TrpfsTer?
ENST00000642589.1:n.4215dup
ENST00000642597.1:n.1067dup
ENST00000642687.1:n.926dup
ENST00000642722.1:n.1726dup
ENST00000642763.1:n.1784dup
ENST00000642793.1:c.*342dup ENSP00000493976.1:n.*342dup
ENST00000642801.1:n.542dup
ENST00000643820.1:n.169dup
ENST00000643963.1:c.*175dup ENSP00000495264.1:n.*175dup
ENST00000644073.1:c.851dup ENSP00000493475.1:p.Cys284TrpfsTer?
ENST00000644074.1:c.890dup ENSP00000496663.1:p.Cys297TrpfsTer?
ENST00000644109.1:c.890dup ENSP00000494952.1:p.Cys297TrpfsTer?
ENST00000644307.1:n.984dup
ENST00000644513.1:c.893dup ENSP00000493819.1:p.Cys298TrpfsTer?
ENST00000644677.1:c.776dup ENSP00000496524.1:p.Cys259TrpfsTer?
ENST00000644876.2:c.893dup MANE Select ENSP00000494040.1:p.Cys298TrpfsTer?
ENST00000644958.1:n.2554dup
ENST00000645080.1:c.*2115dup ENSP00000494767.1:n.*2115dup
ENST00000645120.1:n.2388dup
ENST00000645338.1:n.984dup
ENST00000645380.1:n.2278dup
ENST00000645561.1:n.2069dup
ENST00000645574.1:n.3757dup
ENST00000645589.1:c.893dup ENSP00000494588.1:p.Cys298TrpfsTer?
ENST00000646093.1:n.77dup
ENST00000646107.1:c.776dup ENSP00000494518.1:p.Cys259TrpfsTer?
ENST00000646122.1:c.893dup ENSP00000496222.1:p.Cys298TrpfsTer?
ENST00000646196.1:n.1862dup
ENST00000646223.1:c.*886dup ENSP00000496043.1:n.*886dup
ENST00000646319.1:c.893dup ENSP00000495377.1:p.Cys298TrpfsTer?
ENST00000646390.1:n.3181dup
ENST00000646627.1:c.335dup ENSP00000493795.1:p.Cys112TrpfsTer?
ENST00000646679.1:c.335dup ENSP00000494887.1:p.Cys112TrpfsTer?
ENST00000646822.1:n.1955dup
ENST00000646940.1:n.1067dup
ENST00000647286.1:n.991dup
ENST00000399959.6:c.893dup ENSP00000382840.2:p.Cys298TrpfsTer?
ENST00000441189.3:c.340+1717dup ENSP00000414281.2:n.340+1717dup
ENST00000457138.6:c.845dup ENSP00000392494.2:p.Cys282TrpfsTer?
ENST00000478993.5:c.893dup ENSP00000478443.1:p.Cys298TrpfsTer?
ENST00000542215.5:n.941dup
ENST00000625837.2:c.893dup ENSP00000486306.1:p.Cys298TrpfsTer?
ENST00000626301.2:c.893dup ENSP00000486443.1:p.Cys298TrpfsTer?
ENST00000629496.2:c.893dup ENSP00000487224.1:p.Cys298TrpfsTer?
ENST00000629785.2:c.893dup ENSP00000486516.1:p.Cys298TrpfsTer?
ENST00000630255.2:c.893dup ENSP00000486720.1:p.Cys298TrpfsTer?
ENST00000630370.2:c.893dup ENSP00000487062.1:p.Cys298TrpfsTer?
ENST00000630858.2:c.893dup ENSP00000486514.1:p.Cys298TrpfsTer?
NM_001193416.2:c.893dup NP_001180345.1:p.Cys298TrpfsTer?
NM_001193417.2:c.845dup NP_001180346.1:p.Cys282TrpfsTer?
NM_001356.4:c.893dup NP_001347.3:p.Cys298TrpfsTer?
NR_126093.1:n.1838dup
XM_011543892.1:c.893dup XP_011542194.1:p.Cys298TrpfsTer?
NM_001363819.1:c.335dup NP_001350748.1:p.Cys112TrpfsTer?
XM_011543892.2:c.893dup XP_011542194.1:p.Cys298TrpfsTer?
XM_017029313.1:c.335dup XP_016884802.1:p.Cys112TrpfsTer?
NM_001193416.3:c.893dup NP_001180345.1:p.Cys298TrpfsTer?
NM_001193417.3:c.845dup NP_001180346.1:p.Cys282TrpfsTer?
NM_001356.5:c.893dup MANE Select NP_001347.3:p.Cys298TrpfsTer?