Canonical Allele Identifier: CA412771060
Gene: DDX3X HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41344336T>A , CM000685.2:g.41344336T>A GRCh38
NC_000023.10:g.41203589T>A , CM000685.1:g.41203589T>A GRCh37
NC_000023.9:g.41088533T>A NCBI36
NG_012830.1:g.15939T>A
NG_012830.2:g.15939T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1094T>A ENSP00000496052.2:p.Val365Glu
ENST00000399959.7:c.959T>A ENSP00000382840.3:p.Val320Glu
ENST00000441189.4:c.863T>A ENSP00000414281.3:p.Val288Glu
ENST00000457138.7:c.914T>A ENSP00000392494.2:p.Val305Glu
ENST00000629496.3:c.962T>A ENSP00000487224.1:p.Val321Glu
ENST00000631641.2:n.1005T>A
ENST00000642161.1:n.3161T>A
ENST00000642322.1:c.404T>A ENSP00000496052.1:p.Val135Glu
ENST00000642424.1:c.404T>A ENSP00000496356.1:p.Val135Glu
ENST00000642589.1:n.4284T>A
ENST00000642597.1:n.1136T>A
ENST00000642687.1:n.995T>A
ENST00000642722.1:n.1795T>A
ENST00000642763.1:n.1853T>A
ENST00000642793.1:c.*411T>A ENSP00000493976.1:n.*411T>A
ENST00000642801.1:n.611T>A
ENST00000643820.1:n.238T>A
ENST00000643963.1:c.*244T>A ENSP00000495264.1:n.*244T>A
ENST00000644073.1:c.920T>A ENSP00000493475.1:p.Val307Glu
ENST00000644074.1:c.959T>A ENSP00000496663.1:p.Val320Glu
ENST00000644109.1:c.959T>A ENSP00000494952.1:p.Val320Glu
ENST00000644307.1:n.1053T>A
ENST00000644513.1:c.962T>A ENSP00000493819.1:p.Val321Glu
ENST00000644677.1:c.845T>A ENSP00000496524.1:p.Val282Glu
ENST00000644876.2:c.962T>A MANE Select ENSP00000494040.1:p.Val321Glu
ENST00000644958.1:n.2623T>A
ENST00000645080.1:c.*2184T>A ENSP00000494767.1:n.*2184T>A
ENST00000645120.1:n.2457T>A
ENST00000645338.1:n.1053T>A
ENST00000645380.1:n.2347T>A
ENST00000645561.1:n.2138T>A
ENST00000645574.1:n.3826T>A
ENST00000645589.1:c.962T>A ENSP00000494588.1:p.Val321Glu
ENST00000646093.1:n.146T>A
ENST00000646107.1:c.845T>A ENSP00000494518.1:p.Val282Glu
ENST00000646122.1:c.962T>A ENSP00000496222.1:p.Val321Glu
ENST00000646196.1:n.1931T>A
ENST00000646223.1:c.*955T>A ENSP00000496043.1:n.*955T>A
ENST00000646319.1:c.962T>A ENSP00000495377.1:p.Val321Glu
ENST00000646390.1:n.3250T>A
ENST00000646627.1:c.404T>A ENSP00000493795.1:p.Val135Glu
ENST00000646679.1:c.404T>A ENSP00000494887.1:p.Val135Glu
ENST00000646822.1:n.2024T>A
ENST00000646940.1:n.1136T>A
ENST00000647286.1:n.1060T>A
ENST00000399959.6:c.962T>A ENSP00000382840.2:p.Val321Glu
ENST00000441189.3:c.340+1786T>A ENSP00000414281.2:n.340+1786T>A
ENST00000457138.6:c.914T>A ENSP00000392494.2:p.Val305Glu
ENST00000478993.5:c.962T>A ENSP00000478443.1:p.Val321Glu
ENST00000542215.5:n.1010T>A
ENST00000625837.2:c.962T>A ENSP00000486306.1:p.Val321Glu
ENST00000626301.2:c.962T>A ENSP00000486443.1:p.Val321Glu
ENST00000629496.2:c.962T>A ENSP00000487224.1:p.Val321Glu
ENST00000629785.2:c.962T>A ENSP00000486516.1:p.Val321Glu
ENST00000630255.2:c.962T>A ENSP00000486720.1:p.Val321Glu
ENST00000630370.2:c.962T>A ENSP00000487062.1:p.Val321Glu
ENST00000630858.2:c.962T>A ENSP00000486514.1:p.Val321Glu
NM_001193416.2:c.962T>A NP_001180345.1:p.Val321Glu
NM_001193417.2:c.914T>A NP_001180346.1:p.Val305Glu
NM_001356.4:c.962T>A NP_001347.3:p.Val321Glu
NR_126093.1:n.1907T>A
XM_011543892.1:c.962T>A XP_011542194.1:p.Val321Glu
NM_001363819.1:c.404T>A NP_001350748.1:p.Val135Glu
XM_011543892.2:c.962T>A XP_011542194.1:p.Val321Glu
XM_017029313.1:c.404T>A XP_016884802.1:p.Val135Glu
NM_001193416.3:c.962T>A NP_001180345.1:p.Val321Glu
NM_001193417.3:c.914T>A NP_001180346.1:p.Val305Glu
NM_001356.5:c.962T>A MANE Select NP_001347.3:p.Val321Glu