Canonical Allele Identifier: CA412771503
Gene: DDX3X HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345300T>A , CM000685.2:g.41345300T>A GRCh38
NC_000023.10:g.41204553T>A , CM000685.1:g.41204553T>A GRCh37
NC_000023.9:g.41089497T>A NCBI36
NG_012830.1:g.16903T>A
NG_012830.2:g.16903T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1278T>A ENSP00000496052.2:p.Ser426Arg
ENST00000399959.7:c.1143T>A ENSP00000382840.3:p.Ser381Arg
ENST00000441189.4:c.1047T>A ENSP00000414281.3:p.Ser349Arg
ENST00000457138.7:c.1098T>A ENSP00000392494.2:p.Ser366Arg
ENST00000629496.3:c.1146T>A ENSP00000487224.1:p.Ser382Arg
ENST00000642161.1:n.3345T>A
ENST00000642322.1:c.588T>A ENSP00000496052.1:p.Ser196Arg
ENST00000642424.1:c.588T>A ENSP00000496356.1:p.Ser196Arg
ENST00000642589.1:n.4468T>A
ENST00000642597.1:n.1320T>A
ENST00000642687.1:n.1179T>A
ENST00000642722.1:n.1979T>A
ENST00000642763.1:n.2037T>A
ENST00000642793.1:c.*595T>A ENSP00000493976.1:n.*595T>A
ENST00000642801.1:n.795T>A
ENST00000643820.1:n.422T>A
ENST00000643963.1:c.*428T>A ENSP00000495264.1:n.*428T>A
ENST00000644073.1:c.1104T>A ENSP00000493475.1:p.Ser368Arg
ENST00000644074.1:c.1143T>A ENSP00000496663.1:p.Ser381Arg
ENST00000644109.1:c.1308T>A ENSP00000494952.1:p.Ser436Arg
ENST00000644307.1:n.1237T>A
ENST00000644513.1:c.1146T>A ENSP00000493819.1:p.Ser382Arg
ENST00000644677.1:c.1029T>A ENSP00000496524.1:p.Ser343Arg
ENST00000644876.2:c.1146T>A MANE Select ENSP00000494040.1:p.Ser382Arg
ENST00000644958.1:n.2807T>A
ENST00000645080.1:c.*2368T>A ENSP00000494767.1:n.*2368T>A
ENST00000645120.1:n.2641T>A
ENST00000645338.1:n.1237T>A
ENST00000645380.1:n.2531T>A
ENST00000645561.1:n.2322T>A
ENST00000645574.1:n.4010T>A
ENST00000645589.1:c.1146T>A ENSP00000494588.1:p.Ser382Arg
ENST00000646093.1:n.330T>A
ENST00000646107.1:c.1029T>A ENSP00000494518.1:p.Ser343Arg
ENST00000646122.1:c.1146T>A ENSP00000496222.1:p.Ser382Arg
ENST00000646196.1:n.2115T>A
ENST00000646223.1:c.*1139T>A ENSP00000496043.1:n.*1139T>A
ENST00000646319.1:c.1146T>A ENSP00000495377.1:p.Ser382Arg
ENST00000646390.1:n.3434T>A
ENST00000646627.1:c.588T>A ENSP00000493795.1:p.Ser196Arg
ENST00000646679.1:c.588T>A ENSP00000494887.1:p.Ser196Arg
ENST00000646822.1:n.2208T>A
ENST00000646940.1:n.1320T>A
ENST00000647286.1:n.1244T>A
ENST00000399959.6:c.1146T>A ENSP00000382840.2:p.Ser382Arg
ENST00000441189.3:c.341-2340T>A ENSP00000414281.2:n.341-2340T>A
ENST00000457138.6:c.1098T>A ENSP00000392494.2:p.Ser366Arg
ENST00000478993.5:c.1146T>A ENSP00000478443.1:p.Ser382Arg
ENST00000542215.5:n.1194T>A
ENST00000625837.2:c.1146T>A ENSP00000486306.1:p.Ser382Arg
ENST00000626301.2:c.1146T>A ENSP00000486443.1:p.Ser382Arg
ENST00000629496.2:c.1146T>A ENSP00000487224.1:p.Ser382Arg
ENST00000629785.2:c.1146T>A ENSP00000486516.1:p.Ser382Arg
ENST00000630255.2:c.1146T>A ENSP00000486720.1:p.Ser382Arg
ENST00000630370.2:c.1146T>A ENSP00000487062.1:p.Ser382Arg
ENST00000630858.2:c.1146T>A ENSP00000486514.1:p.Ser382Arg
NM_001193416.2:c.1146T>A NP_001180345.1:p.Ser382Arg
NM_001193417.2:c.1098T>A NP_001180346.1:p.Ser366Arg
NM_001356.4:c.1146T>A NP_001347.3:p.Ser382Arg
NR_126093.1:n.2091T>A
XM_011543892.1:c.1146T>A XP_011542194.1:p.Ser382Arg
NM_001363819.1:c.588T>A NP_001350748.1:p.Ser196Arg
XM_011543892.2:c.1146T>A XP_011542194.1:p.Ser382Arg
XM_017029313.1:c.588T>A XP_016884802.1:p.Ser196Arg
NM_001193416.3:c.1146T>A NP_001180345.1:p.Ser382Arg
NM_001193417.3:c.1098T>A NP_001180346.1:p.Ser366Arg
NM_001356.5:c.1146T>A MANE Select NP_001347.3:p.Ser382Arg