Canonical Allele Identifier: CA16621385
Gene: DDX3X HGNC NCBI

Linked Data

ClinVar Variation Id: 419725
ClinVar RCV Id: RCV000480302
dbSNP Id: rs1064794068

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345298A>C , CM000685.2:g.41345298A>C GRCh38
NC_000023.10:g.41204551A>C , CM000685.1:g.41204551A>C GRCh37
NC_000023.9:g.41089495A>C NCBI36
NG_012830.1:g.16901A>C
NG_012830.2:g.16901A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000642322.2:c.1276A>C ENSP00000496052.2:p.Ser426Arg
ENST00000399959.7:c.1141A>C ENSP00000382840.3:p.Ser381Arg
ENST00000441189.4:c.1045A>C ENSP00000414281.3:p.Ser349Arg
ENST00000457138.7:c.1096A>C ENSP00000392494.2:p.Ser366Arg
ENST00000629496.3:c.1144A>C ENSP00000487224.1:p.Ser382Arg
ENST00000642161.1:n.3343A>C
ENST00000642322.1:c.586A>C ENSP00000496052.1:p.Ser196Arg
ENST00000642424.1:c.586A>C ENSP00000496356.1:p.Ser196Arg
ENST00000642589.1:n.4466A>C
ENST00000642597.1:n.1318A>C
ENST00000642687.1:n.1177A>C
ENST00000642722.1:n.1977A>C
ENST00000642763.1:n.2035A>C
ENST00000642793.1:c.*593A>C ENSP00000493976.1:n.*593A>C
ENST00000642801.1:n.793A>C
ENST00000643820.1:n.420A>C
ENST00000643963.1:c.*426A>C ENSP00000495264.1:n.*426A>C
ENST00000644073.1:c.1102A>C ENSP00000493475.1:p.Ser368Arg
ENST00000644074.1:c.1141A>C ENSP00000496663.1:p.Ser381Arg
ENST00000644109.1:c.1306A>C ENSP00000494952.1:p.Ser436Arg
ENST00000644307.1:n.1235A>C
ENST00000644513.1:c.1144A>C ENSP00000493819.1:p.Ser382Arg
ENST00000644677.1:c.1027A>C ENSP00000496524.1:p.Ser343Arg
ENST00000644876.2:c.1144A>C MANE Select ENSP00000494040.1:p.Ser382Arg
ENST00000644958.1:n.2805A>C
ENST00000645080.1:c.*2366A>C ENSP00000494767.1:n.*2366A>C
ENST00000645120.1:n.2639A>C
ENST00000645338.1:n.1235A>C
ENST00000645380.1:n.2529A>C
ENST00000645561.1:n.2320A>C
ENST00000645574.1:n.4008A>C
ENST00000645589.1:c.1144A>C ENSP00000494588.1:p.Ser382Arg
ENST00000646093.1:n.328A>C
ENST00000646107.1:c.1027A>C ENSP00000494518.1:p.Ser343Arg
ENST00000646122.1:c.1144A>C ENSP00000496222.1:p.Ser382Arg
ENST00000646196.1:n.2113A>C
ENST00000646223.1:c.*1137A>C ENSP00000496043.1:n.*1137A>C
ENST00000646319.1:c.1144A>C ENSP00000495377.1:p.Ser382Arg
ENST00000646390.1:n.3432A>C
ENST00000646627.1:c.586A>C ENSP00000493795.1:p.Ser196Arg
ENST00000646679.1:c.586A>C ENSP00000494887.1:p.Ser196Arg
ENST00000646822.1:n.2206A>C
ENST00000646940.1:n.1318A>C
ENST00000647286.1:n.1242A>C
ENST00000399959.6:c.1144A>C ENSP00000382840.2:p.Ser382Arg
ENST00000441189.3:c.341-2342A>C ENSP00000414281.2:n.341-2342A>C
ENST00000457138.6:c.1096A>C ENSP00000392494.2:p.Ser366Arg
ENST00000478993.5:c.1144A>C ENSP00000478443.1:p.Ser382Arg
ENST00000542215.5:n.1192A>C
ENST00000625837.2:c.1144A>C ENSP00000486306.1:p.Ser382Arg
ENST00000626301.2:c.1144A>C ENSP00000486443.1:p.Ser382Arg
ENST00000629496.2:c.1144A>C ENSP00000487224.1:p.Ser382Arg
ENST00000629785.2:c.1144A>C ENSP00000486516.1:p.Ser382Arg
ENST00000630255.2:c.1144A>C ENSP00000486720.1:p.Ser382Arg
ENST00000630370.2:c.1144A>C ENSP00000487062.1:p.Ser382Arg
ENST00000630858.2:c.1144A>C ENSP00000486514.1:p.Ser382Arg
NM_001193416.2:c.1144A>C NP_001180345.1:p.Ser382Arg
NM_001193417.2:c.1096A>C NP_001180346.1:p.Ser366Arg
NM_001356.4:c.1144A>C NP_001347.3:p.Ser382Arg
NR_126093.1:n.2089A>C
XM_011543892.1:c.1144A>C XP_011542194.1:p.Ser382Arg
NM_001363819.1:c.586A>C NP_001350748.1:p.Ser196Arg
XM_011543892.2:c.1144A>C XP_011542194.1:p.Ser382Arg
XM_017029313.1:c.586A>C XP_016884802.1:p.Ser196Arg
NM_001193416.3:c.1144A>C NP_001180345.1:p.Ser382Arg
NM_001193417.3:c.1096A>C NP_001180346.1:p.Ser366Arg
NM_001356.5:c.1144A>C MANE Select NP_001347.3:p.Ser382Arg