Canonical Allele Identifier: CA2425881026
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345187G= , CM000685.2:g.41345187G= GRCh38
NC_000023.10:g.41204440G= , CM000685.1:g.41204440G= GRCh37
NC_000023.9:g.41089384G= NCBI36
NG_012830.1:g.16790G=
NG_012830.2:g.16790G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1165G= ENSP00000496052.2:p.Val389=
ENST00000399959.7:c.1030G= ENSP00000382840.3:p.Val344=
ENST00000441189.4:c.934G= ENSP00000414281.3:p.Val312=
ENST00000457138.7:c.985G= ENSP00000392494.2:p.Val329=
ENST00000629496.3:c.1033G= ENSP00000487224.1:p.Val345=
ENST00000642161.1:n.3232G=
ENST00000642322.1:c.475G= ENSP00000496052.1:p.Val159=
ENST00000642424.1:c.475G= ENSP00000496356.1:p.Val159=
ENST00000642589.1:n.4355G=
ENST00000642597.1:n.1207G=
ENST00000642687.1:n.1066G=
ENST00000642722.1:n.1866G=
ENST00000642763.1:n.1924G=
ENST00000642793.1:c.*482G= ENSP00000493976.1:n.*482G=
ENST00000642801.1:n.682G=
ENST00000643820.1:n.309G=
ENST00000643963.1:c.*315G= ENSP00000495264.1:n.*315G=
ENST00000644073.1:c.991G= ENSP00000493475.1:p.Val331=
ENST00000644074.1:c.1030G= ENSP00000496663.1:p.Val344=
ENST00000644109.1:c.1195G= ENSP00000494952.1:p.Val399=
ENST00000644307.1:n.1124G=
ENST00000644513.1:c.1033G= ENSP00000493819.1:p.Val345=
ENST00000644677.1:c.916G= ENSP00000496524.1:p.Val306=
ENST00000644876.2:c.1033G= MANE Select ENSP00000494040.1:p.Val345=
ENST00000644958.1:n.2694G=
ENST00000645080.1:c.*2255G= ENSP00000494767.1:n.*2255G=
ENST00000645120.1:n.2528G=
ENST00000645338.1:n.1124G=
ENST00000645380.1:n.2418G=
ENST00000645561.1:n.2209G=
ENST00000645574.1:n.3897G=
ENST00000645589.1:c.1033G= ENSP00000494588.1:p.Val345=
ENST00000646093.1:n.217G=
ENST00000646107.1:c.916G= ENSP00000494518.1:p.Val306=
ENST00000646122.1:c.1033G= ENSP00000496222.1:p.Val345=
ENST00000646196.1:n.2002G=
ENST00000646223.1:c.*1026G= ENSP00000496043.1:n.*1026G=
ENST00000646319.1:c.1033G= ENSP00000495377.1:p.Val345=
ENST00000646390.1:n.3321G=
ENST00000646627.1:c.475G= ENSP00000493795.1:p.Val159=
ENST00000646679.1:c.475G= ENSP00000494887.1:p.Val159=
ENST00000646822.1:n.2095G=
ENST00000646940.1:n.1207G=
ENST00000647286.1:n.1131G=
ENST00000399959.6:c.1033G= ENSP00000382840.2:p.Val345=
ENST00000441189.3:c.341-2453G= ENSP00000414281.2:n.341-2453G=
ENST00000457138.6:c.985G= ENSP00000392494.2:p.Val329=
ENST00000478993.5:c.1033G= ENSP00000478443.1:p.Val345=
ENST00000542215.5:n.1081G=
ENST00000625837.2:c.1033G= ENSP00000486306.1:p.Val345=
ENST00000626301.2:c.1033G= ENSP00000486443.1:p.Val345=
ENST00000629496.2:c.1033G= ENSP00000487224.1:p.Val345=
ENST00000629785.2:c.1033G= ENSP00000486516.1:p.Val345=
ENST00000630255.2:c.1033G= ENSP00000486720.1:p.Val345=
ENST00000630370.2:c.1033G= ENSP00000487062.1:p.Val345=
ENST00000630858.2:c.1033G= ENSP00000486514.1:p.Val345=
NM_001193416.2:c.1033G= NP_001180345.1:p.Val345=
NM_001193417.2:c.985G= NP_001180346.1:p.Val329=
NM_001356.4:c.1033G= NP_001347.3:p.Val345=
NR_126093.1:n.1978G=
XM_011543892.1:c.1033G= XP_011542194.1:p.Val345=
NM_001363819.1:c.475G= NP_001350748.1:p.Val159=
XM_011543892.2:c.1033G= XP_011542194.1:p.Val345=
XM_017029313.1:c.475G= XP_016884802.1:p.Val159=
NM_001193416.3:c.1033G= NP_001180345.1:p.Val345=
NM_001193417.3:c.985G= NP_001180346.1:p.Val329=
NM_001356.5:c.1033G= MANE Select NP_001347.3:p.Val345=