Canonical Allele Identifier: CA2425880619
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41344359G= , CM000685.2:g.41344359G= GRCh38
NC_000023.10:g.41203612G= , CM000685.1:g.41203612G= GRCh37
NC_000023.9:g.41088556G= NCBI36
NG_012830.1:g.15962G=
NG_012830.2:g.15962G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1117G= ENSP00000496052.2:p.Asp373=
ENST00000399959.7:c.982G= ENSP00000382840.3:p.Asp328=
ENST00000441189.4:c.886G= ENSP00000414281.3:p.Asp296=
ENST00000457138.7:c.937G= ENSP00000392494.2:p.Asp313=
ENST00000629496.3:c.985G= ENSP00000487224.1:p.Asp329=
ENST00000631641.2:n.1028G=
ENST00000642161.1:n.3184G=
ENST00000642322.1:c.427G= ENSP00000496052.1:p.Asp143=
ENST00000642424.1:c.427G= ENSP00000496356.1:p.Asp143=
ENST00000642589.1:n.4307G=
ENST00000642597.1:n.1159G=
ENST00000642687.1:n.1018G=
ENST00000642722.1:n.1818G=
ENST00000642763.1:n.1876G=
ENST00000642793.1:c.*434G= ENSP00000493976.1:n.*434G=
ENST00000642801.1:n.634G=
ENST00000643820.1:n.261G=
ENST00000643963.1:c.*267G= ENSP00000495264.1:n.*267G=
ENST00000644073.1:c.943G= ENSP00000493475.1:p.Asp315=
ENST00000644074.1:c.982G= ENSP00000496663.1:p.Asp328=
ENST00000644109.1:c.982G= ENSP00000494952.1:p.Asp328=
ENST00000644307.1:n.1076G=
ENST00000644513.1:c.985G= ENSP00000493819.1:p.Asp329=
ENST00000644677.1:c.868G= ENSP00000496524.1:p.Asp290=
ENST00000644876.2:c.985G= MANE Select ENSP00000494040.1:p.Asp329=
ENST00000644958.1:n.2646G=
ENST00000645080.1:c.*2207G= ENSP00000494767.1:n.*2207G=
ENST00000645120.1:n.2480G=
ENST00000645338.1:n.1076G=
ENST00000645380.1:n.2370G=
ENST00000645561.1:n.2161G=
ENST00000645574.1:n.3849G=
ENST00000645589.1:c.985G= ENSP00000494588.1:p.Asp329=
ENST00000646093.1:n.169G=
ENST00000646107.1:c.868G= ENSP00000494518.1:p.Asp290=
ENST00000646122.1:c.985G= ENSP00000496222.1:p.Asp329=
ENST00000646196.1:n.1954G=
ENST00000646223.1:c.*978G= ENSP00000496043.1:n.*978G=
ENST00000646319.1:c.985G= ENSP00000495377.1:p.Asp329=
ENST00000646390.1:n.3273G=
ENST00000646627.1:c.427G= ENSP00000493795.1:p.Asp143=
ENST00000646679.1:c.427G= ENSP00000494887.1:p.Asp143=
ENST00000646822.1:n.2047G=
ENST00000646940.1:n.1159G=
ENST00000647286.1:n.1083G=
ENST00000399959.6:c.985G= ENSP00000382840.2:p.Asp329=
ENST00000441189.3:c.340+1809G= ENSP00000414281.2:n.340+1809G=
ENST00000457138.6:c.937G= ENSP00000392494.2:p.Asp313=
ENST00000478993.5:c.985G= ENSP00000478443.1:p.Asp329=
ENST00000542215.5:n.1033G=
ENST00000625837.2:c.985G= ENSP00000486306.1:p.Asp329=
ENST00000626301.2:c.985G= ENSP00000486443.1:p.Asp329=
ENST00000629496.2:c.985G= ENSP00000487224.1:p.Asp329=
ENST00000629785.2:c.985G= ENSP00000486516.1:p.Asp329=
ENST00000630255.2:c.985G= ENSP00000486720.1:p.Asp329=
ENST00000630370.2:c.985G= ENSP00000487062.1:p.Asp329=
ENST00000630858.2:c.985G= ENSP00000486514.1:p.Asp329=
NM_001193416.2:c.985G= NP_001180345.1:p.Asp329=
NM_001193417.2:c.937G= NP_001180346.1:p.Asp313=
NM_001356.4:c.985G= NP_001347.3:p.Asp329=
NR_126093.1:n.1930G=
XM_011543892.1:c.985G= XP_011542194.1:p.Asp329=
NM_001363819.1:c.427G= NP_001350748.1:p.Asp143=
XM_011543892.2:c.985G= XP_011542194.1:p.Asp329=
XM_017029313.1:c.427G= XP_016884802.1:p.Asp143=
NM_001193416.3:c.985G= NP_001180345.1:p.Asp329=
NM_001193417.3:c.937G= NP_001180346.1:p.Asp313=
NM_001356.5:c.985G= MANE Select NP_001347.3:p.Asp329=