Canonical Allele Identifier: CA2425880567
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41344244A= , CM000685.2:g.41344244A= GRCh38
NC_000023.10:g.41203497A= , CM000685.1:g.41203497A= GRCh37
NC_000023.9:g.41088441A= NCBI36
NG_012830.1:g.15847A=
NG_012830.2:g.15847A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642322.2:c.1002A= ENSP00000496052.2:p.Ser334=
ENST00000399959.7:c.867A= ENSP00000382840.3:p.Ser289=
ENST00000441189.4:c.771A= ENSP00000414281.3:p.Ser257=
ENST00000457138.7:c.822A= ENSP00000392494.2:p.Ser274=
ENST00000629496.3:c.870A= ENSP00000487224.1:p.Ser290=
ENST00000631641.2:n.913A=
ENST00000642161.1:n.3069A=
ENST00000642322.1:c.312A= ENSP00000496052.1:p.Ser104=
ENST00000642424.1:c.312A= ENSP00000496356.1:p.Ser104=
ENST00000642589.1:n.4192A=
ENST00000642597.1:n.1044A=
ENST00000642687.1:n.903A=
ENST00000642722.1:n.1703A=
ENST00000642763.1:n.1761A=
ENST00000642793.1:c.*319A= ENSP00000493976.1:n.*319A=
ENST00000642801.1:n.519A=
ENST00000643820.1:n.146A=
ENST00000643963.1:c.*152A= ENSP00000495264.1:n.*152A=
ENST00000644073.1:c.828A= ENSP00000493475.1:p.Ser276=
ENST00000644074.1:c.867A= ENSP00000496663.1:p.Ser289=
ENST00000644109.1:c.867A= ENSP00000494952.1:p.Ser289=
ENST00000644307.1:n.961A=
ENST00000644513.1:c.870A= ENSP00000493819.1:p.Ser290=
ENST00000644677.1:c.753A= ENSP00000496524.1:p.Ser251=
ENST00000644876.2:c.870A= MANE Select ENSP00000494040.1:p.Ser290=
ENST00000644958.1:n.2531A=
ENST00000645080.1:c.*2092A= ENSP00000494767.1:n.*2092A=
ENST00000645120.1:n.2365A=
ENST00000645338.1:n.961A=
ENST00000645380.1:n.2255A=
ENST00000645561.1:n.2046A=
ENST00000645574.1:n.3734A=
ENST00000645589.1:c.870A= ENSP00000494588.1:p.Ser290=
ENST00000646093.1:n.54A=
ENST00000646107.1:c.753A= ENSP00000494518.1:p.Ser251=
ENST00000646122.1:c.870A= ENSP00000496222.1:p.Ser290=
ENST00000646196.1:n.1839A=
ENST00000646223.1:c.*863A= ENSP00000496043.1:n.*863A=
ENST00000646319.1:c.870A= ENSP00000495377.1:p.Ser290=
ENST00000646390.1:n.3158A=
ENST00000646627.1:c.312A= ENSP00000493795.1:p.Ser104=
ENST00000646679.1:c.312A= ENSP00000494887.1:p.Ser104=
ENST00000646822.1:n.1932A=
ENST00000646940.1:n.1044A=
ENST00000647286.1:n.968A=
ENST00000399959.6:c.870A= ENSP00000382840.2:p.Ser290=
ENST00000441189.3:c.340+1694A= ENSP00000414281.2:n.340+1694A=
ENST00000457138.6:c.822A= ENSP00000392494.2:p.Ser274=
ENST00000478993.5:c.870A= ENSP00000478443.1:p.Ser290=
ENST00000542215.5:n.918A=
ENST00000625837.2:c.870A= ENSP00000486306.1:p.Ser290=
ENST00000626301.2:c.870A= ENSP00000486443.1:p.Ser290=
ENST00000629496.2:c.870A= ENSP00000487224.1:p.Ser290=
ENST00000629785.2:c.870A= ENSP00000486516.1:p.Ser290=
ENST00000630255.2:c.870A= ENSP00000486720.1:p.Ser290=
ENST00000630370.2:c.870A= ENSP00000487062.1:p.Ser290=
ENST00000630858.2:c.870A= ENSP00000486514.1:p.Ser290=
NM_001193416.2:c.870A= NP_001180345.1:p.Ser290=
NM_001193417.2:c.822A= NP_001180346.1:p.Ser274=
NM_001356.4:c.870A= NP_001347.3:p.Ser290=
NR_126093.1:n.1815A=
XM_011543892.1:c.870A= XP_011542194.1:p.Ser290=
NM_001363819.1:c.312A= NP_001350748.1:p.Ser104=
XM_011543892.2:c.870A= XP_011542194.1:p.Ser290=
XM_017029313.1:c.312A= XP_016884802.1:p.Ser104=
NM_001193416.3:c.870A= NP_001180345.1:p.Ser290=
NM_001193417.3:c.822A= NP_001180346.1:p.Ser274=
NM_001356.5:c.870A= MANE Select NP_001347.3:p.Ser290=