Canonical Allele Identifier: CA412764800
Gene: DDX3X HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41341520G>T , CM000685.2:g.41341520G>T GRCh38
NC_000023.10:g.41200773G>T , CM000685.1:g.41200773G>T GRCh37
NC_000023.9:g.41085717G>T NCBI36
NG_012830.1:g.13123G>T
NG_012830.2:g.13123G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.320G>T ENSP00000496052.2:p.Ser107Ile
ENST00000399959.7:c.185G>T ENSP00000382840.3:p.Ser62Ile
ENST00000441189.4:c.188G>T ENSP00000414281.3:p.Ser63Ile
ENST00000457138.7:c.140G>T ENSP00000392494.2:p.Ser47Ile
ENST00000611546.2:n.494G>T
ENST00000615313.5:c.146G>T ENSP00000496257.1:p.Ser49Ile
ENST00000622198.5:n.345G>T
ENST00000629496.3:c.188G>T ENSP00000487224.1:p.Ser63Ile
ENST00000631641.2:n.231G>T
ENST00000642161.1:n.1509G>T
ENST00000642322.1:c.-371G>T ENSP00000496052.1:n.-371G>T
ENST00000642424.1:c.-371G>T ENSP00000496356.1:n.-371G>T
ENST00000642589.1:n.1578G>T
ENST00000642597.1:n.279G>T
ENST00000642624.1:n.78G>T
ENST00000642722.1:n.279G>T
ENST00000642763.1:n.201G>T
ENST00000642793.1:c.188G>T ENSP00000493976.1:p.Ser63Ile
ENST00000643963.1:c.188G>T ENSP00000495264.1:p.Ser63Ile
ENST00000644073.1:c.146G>T ENSP00000493475.1:p.Ser49Ile
ENST00000644074.1:c.185G>T ENSP00000496663.1:p.Ser62Ile
ENST00000644109.1:c.185G>T ENSP00000494952.1:p.Ser62Ile
ENST00000644260.1:n.16G>T
ENST00000644307.1:n.279G>T
ENST00000644513.1:c.188G>T ENSP00000493819.1:p.Ser63Ile
ENST00000644677.1:c.71G>T ENSP00000496524.1:p.Ser24Ile
ENST00000644876.2:c.188G>T MANE Select ENSP00000494040.1:p.Ser63Ile
ENST00000644958.1:n.1849G>T
ENST00000645080.1:c.*1410G>T ENSP00000494767.1:n.*1410G>T
ENST00000645120.1:n.1683G>T
ENST00000645253.1:n.1611G>T
ENST00000645338.1:n.279G>T
ENST00000645380.1:n.1573G>T
ENST00000645561.1:n.279G>T
ENST00000645574.1:n.1499G>T
ENST00000645589.1:c.188G>T ENSP00000494588.1:p.Ser63Ile
ENST00000645783.1:c.*1287G>T ENSP00000494905.1:n.*1287G>T
ENST00000646107.1:c.71G>T ENSP00000494518.1:p.Ser24Ile
ENST00000646122.1:c.188G>T ENSP00000496222.1:p.Ser63Ile
ENST00000646196.1:n.279G>T
ENST00000646223.1:c.*181G>T ENSP00000496043.1:n.*181G>T
ENST00000646319.1:c.188G>T ENSP00000495377.1:p.Ser63Ile
ENST00000646390.1:n.1515G>T
ENST00000646627.1:c.-371G>T ENSP00000493795.1:n.-371G>T
ENST00000646679.1:c.-371G>T ENSP00000494887.1:n.-371G>T
ENST00000646822.1:n.279G>T
ENST00000646940.1:n.279G>T
ENST00000647219.1:n.173G>T
ENST00000399959.6:c.188G>T ENSP00000382840.2:p.Ser63Ile
ENST00000441189.3:c.188G>T ENSP00000414281.2:p.Ser63Ile
ENST00000457138.6:c.140G>T ENSP00000392494.2:p.Ser47Ile
ENST00000478993.5:c.188G>T ENSP00000478443.1:p.Ser63Ile
ENST00000542215.5:n.322G>T
ENST00000611546.1:n.320G>T
ENST00000615313.4:n.424G>T
ENST00000615742.4:c.188G>T ENSP00000480647.1:p.Ser63Ile
ENST00000622198.4:n.289G>T
ENST00000625837.2:c.188G>T ENSP00000486306.1:p.Ser63Ile
ENST00000626301.2:c.188G>T ENSP00000486443.1:p.Ser63Ile
ENST00000629496.2:c.188G>T ENSP00000487224.1:p.Ser63Ile
ENST00000629785.2:c.188G>T ENSP00000486516.1:p.Ser63Ile
ENST00000630255.2:c.188G>T ENSP00000486720.1:p.Ser63Ile
ENST00000630370.2:c.188G>T ENSP00000487062.1:p.Ser63Ile
ENST00000630858.2:c.188G>T ENSP00000486514.1:p.Ser63Ile
ENST00000631641.1:c.140G>T ENSP00000488854.1:p.Ser47Ile
NM_001193416.2:c.188G>T NP_001180345.1:p.Ser63Ile
NM_001193417.2:c.140G>T NP_001180346.1:p.Ser47Ile
NM_001356.4:c.188G>T NP_001347.3:p.Ser63Ile
NR_126093.1:n.1133G>T
XM_011543892.1:c.188G>T XP_011542194.1:p.Ser63Ile
NM_001363819.1:c.-371G>T NP_001350748.1:n.-371G>T
XM_011543892.2:c.188G>T XP_011542194.1:p.Ser63Ile
XM_017029313.1:c.-371G>T XP_016884802.1:n.-371G>T
NM_001193416.3:c.188G>T NP_001180345.1:p.Ser63Ile
NM_001193417.3:c.140G>T NP_001180346.1:p.Ser47Ile
NM_001356.5:c.188G>T MANE Select NP_001347.3:p.Ser63Ile