Canonical Allele Identifier: CA16621377
Gene: DDX3X HGNC NCBI

Linked Data

ClinVar Variation Id: 419413
dbSNP Id: rs1064793858

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41339051C>G , CM000685.2:g.41339051C>G GRCh38
NC_000023.10:g.41198304C>G , CM000685.1:g.41198304C>G GRCh37
NC_000023.9:g.41083248C>G NCBI36
NG_012830.1:g.10654C>G
NG_012830.2:g.10654C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642322.2:c.251C>G ENSP00000496052.2:p.Pro84Arg
ENST00000399959.7:c.116C>G ENSP00000382840.3:p.Pro39Arg
ENST00000441189.4:c.119C>G ENSP00000414281.3:p.Pro40Arg
ENST00000457138.7:c.103+1586C>G ENSP00000392494.2:n.103+1586C>G
ENST00000480592.6:n.1780C>G
ENST00000610559.5:n.510C>G
ENST00000611546.2:n.425C>G
ENST00000615313.5:c.77C>G ENSP00000496257.1:p.Pro26Arg
ENST00000622198.5:n.276C>G
ENST00000629496.3:c.119C>G ENSP00000487224.1:p.Pro40Arg
ENST00000631641.2:n.194+1586C>G
ENST00000642322.1:c.-440C>G ENSP00000496052.1:n.-440C>G
ENST00000642597.1:n.210C>G
ENST00000642624.1:n.42-2433C>G
ENST00000642722.1:n.210C>G
ENST00000642793.1:c.119C>G ENSP00000493976.1:p.Pro40Arg
ENST00000643963.1:c.119C>G ENSP00000495264.1:p.Pro40Arg
ENST00000644073.1:c.77C>G ENSP00000493475.1:p.Pro26Arg
ENST00000644074.1:c.116C>G ENSP00000496663.1:p.Pro39Arg
ENST00000644109.1:c.116C>G ENSP00000494952.1:p.Pro39Arg
ENST00000644307.1:n.210C>G
ENST00000644513.1:c.119C>G ENSP00000493819.1:p.Pro40Arg
ENST00000644677.1:c.-178C>G ENSP00000496524.1:n.-178C>G
ENST00000644876.2:c.119C>G MANE Select ENSP00000494040.1:p.Pro40Arg
ENST00000644958.1:n.1780C>G
ENST00000645080.1:c.*1341C>G ENSP00000494767.1:n.*1341C>G
ENST00000645120.1:n.1614C>G
ENST00000645338.1:n.210C>G
ENST00000645561.1:n.210C>G
ENST00000645589.1:c.119C>G ENSP00000494588.1:p.Pro40Arg
ENST00000645783.1:c.*1218C>G ENSP00000494905.1:n.*1218C>G
ENST00000646107.1:c.-178C>G ENSP00000494518.1:n.-178C>G
ENST00000646122.1:c.119C>G ENSP00000496222.1:p.Pro40Arg
ENST00000646196.1:n.210C>G
ENST00000646223.1:c.119C>G ENSP00000496043.1:p.Pro40Arg
ENST00000646319.1:c.119C>G ENSP00000495377.1:p.Pro40Arg
ENST00000646627.1:c.-440C>G ENSP00000493795.1:n.-440C>G
ENST00000646822.1:n.210C>G
ENST00000646940.1:n.210C>G
ENST00000647219.1:n.137-2433C>G
ENST00000399959.6:c.119C>G ENSP00000382840.2:p.Pro40Arg
ENST00000441189.3:c.119C>G ENSP00000414281.2:p.Pro40Arg
ENST00000457138.6:c.103+1586C>G ENSP00000392494.2:n.103+1586C>G
ENST00000478993.5:c.119C>G ENSP00000478443.1:p.Pro40Arg
ENST00000542215.5:n.253C>G
ENST00000610559.4:n.510C>G
ENST00000611546.1:n.251C>G
ENST00000615313.4:n.355C>G
ENST00000615742.4:c.119C>G ENSP00000480647.1:p.Pro40Arg
ENST00000622198.4:n.220C>G
ENST00000625837.2:c.119C>G ENSP00000486306.1:p.Pro40Arg
ENST00000626301.2:c.119C>G ENSP00000486443.1:p.Pro40Arg
ENST00000629496.2:c.119C>G ENSP00000487224.1:p.Pro40Arg
ENST00000629785.2:c.119C>G ENSP00000486516.1:p.Pro40Arg
ENST00000630255.2:c.119C>G ENSP00000486720.1:p.Pro40Arg
ENST00000630370.2:c.119C>G ENSP00000487062.1:p.Pro40Arg
ENST00000630858.2:c.119C>G ENSP00000486514.1:p.Pro40Arg
ENST00000631641.1:c.103+1586C>G ENSP00000488854.1:n.103+1586C>G
NM_001193416.2:c.119C>G NP_001180345.1:p.Pro40Arg
NM_001193417.2:c.103+1586C>G NP_001180346.1:n.103+1586C>G
NM_001356.4:c.119C>G NP_001347.3:p.Pro40Arg
NR_126093.1:n.1064C>G
XM_011543892.1:c.119C>G XP_011542194.1:p.Pro40Arg
NM_001363819.1:c.-440C>G NP_001350748.1:n.-440C>G
XM_011543892.2:c.119C>G XP_011542194.1:p.Pro40Arg
XM_017029313.1:c.-440C>G XP_016884802.1:n.-440C>G
NM_001193416.3:c.119C>G NP_001180345.1:p.Pro40Arg
NM_001193417.3:c.103+1586C>G NP_001180346.1:n.103+1586C>G
NM_001356.5:c.119C>G MANE Select NP_001347.3:p.Pro40Arg