Canonical Allele Identifier: CA2425881510
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346603G= , CM000685.2:g.41346603G= GRCh38
NC_000023.10:g.41205856G= , CM000685.1:g.41205856G= GRCh37
NC_000023.9:g.41090800G= NCBI36
NG_012830.1:g.18206G=
NG_012830.2:g.18206G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1728G= ENSP00000496052.2:p.Thr576=
ENST00000399959.7:c.1593G= ENSP00000382840.3:p.Thr531=
ENST00000441189.4:c.1497G= ENSP00000414281.3:p.Thr499=
ENST00000457138.7:c.1548G= ENSP00000392494.2:p.Thr516=
ENST00000611968.2:c.190G=
ENST00000616050.3:c.344G=
ENST00000629496.3:c.1596G= ENSP00000487224.1:p.Thr532=
ENST00000642161.1:n.3795G=
ENST00000642322.1:c.1038G= ENSP00000496052.1:p.Thr346=
ENST00000642424.1:c.1038G= ENSP00000496356.1:p.Thr346=
ENST00000642589.1:n.4918G=
ENST00000642597.1:n.1770G=
ENST00000642687.1:n.1629G=
ENST00000642722.1:n.2429G=
ENST00000642763.1:n.2487G=
ENST00000642793.1:c.*1045G= ENSP00000493976.1:n.*1045G=
ENST00000642801.1:n.1245G=
ENST00000643820.1:n.966G=
ENST00000643963.1:c.*878G= ENSP00000495264.1:n.*878G=
ENST00000644073.1:c.1554G= ENSP00000493475.1:p.Thr518=
ENST00000644074.1:c.1593G= ENSP00000496663.1:p.Thr531=
ENST00000644109.1:c.1758G= ENSP00000494952.1:p.Thr586=
ENST00000644307.1:n.1766G=
ENST00000644513.1:c.1596G= ENSP00000493819.1:p.Thr532=
ENST00000644677.1:c.1479G= ENSP00000496524.1:p.Thr493=
ENST00000644876.2:c.1596G= MANE Select ENSP00000494040.1:p.Thr532=
ENST00000644958.1:n.3257G=
ENST00000645080.1:c.*2818G= ENSP00000494767.1:n.*2818G=
ENST00000645120.1:n.3091G=
ENST00000645338.1:n.1766G=
ENST00000645380.1:n.3060G=
ENST00000645561.1:n.2772G=
ENST00000645574.1:n.4460G=
ENST00000645589.1:c.*95G= ENSP00000494588.1:n.*95G=
ENST00000646107.1:c.1479G= ENSP00000494518.1:p.Thr493=
ENST00000646122.1:c.1596G= ENSP00000496222.1:p.Thr532=
ENST00000646196.1:n.2565G=
ENST00000646223.1:c.*1589G= ENSP00000496043.1:n.*1589G=
ENST00000646319.1:c.1596G= ENSP00000495377.1:p.Thr532=
ENST00000646390.1:n.3884G=
ENST00000646627.1:c.1038G= ENSP00000493795.1:p.Thr346=
ENST00000646679.1:c.1038G= ENSP00000494887.1:p.Thr346=
ENST00000646822.1:n.2658G=
ENST00000646940.1:n.1770G=
ENST00000647286.1:n.1694G=
ENST00000647477.1:n.335G=
ENST00000399959.6:c.1596G= ENSP00000382840.2:p.Thr532=
ENST00000441189.3:c.341-1037G= ENSP00000414281.2:n.341-1037G=
ENST00000457138.6:c.1548G= ENSP00000392494.2:p.Thr516=
ENST00000478993.5:c.1596G= ENSP00000478443.1:p.Thr532=
ENST00000611968.1:c.38G=
ENST00000616050.2:c.149G=
ENST00000625837.2:c.1596G= ENSP00000486306.1:p.Thr532=
ENST00000626301.2:c.1596G= ENSP00000486443.1:p.Thr532=
ENST00000629496.2:c.1596G= ENSP00000487224.1:p.Thr532=
ENST00000629785.2:c.1596G= ENSP00000486516.1:p.Thr532=
ENST00000630255.2:c.1596G= ENSP00000486720.1:p.Thr532=
ENST00000630370.2:c.1596G= ENSP00000487062.1:p.Thr532=
ENST00000630858.2:c.1596G= ENSP00000486514.1:p.Thr532=
NM_001193416.2:c.1596G= NP_001180345.1:p.Thr532=
NM_001193417.2:c.1548G= NP_001180346.1:p.Thr516=
NM_001356.4:c.1596G= NP_001347.3:p.Thr532=
NR_126093.1:n.2541G=
XM_011543892.1:c.1596G= XP_011542194.1:p.Thr532=
NM_001363819.1:c.1038G= NP_001350748.1:p.Thr346=
XM_011543892.2:c.1596G= XP_011542194.1:p.Thr532=
XM_017029313.1:c.1038G= XP_016884802.1:p.Thr346=
NM_001193416.3:c.1596G= NP_001180345.1:p.Thr532=
NM_001193417.3:c.1548G= NP_001180346.1:p.Thr516=
NM_001356.5:c.1596G= MANE Select NP_001347.3:p.Thr532=