Canonical Allele Identifier: CA2425881413
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346397T= , CM000685.2:g.41346397T= GRCh38
NC_000023.10:g.41205650T= , CM000685.1:g.41205650T= GRCh37
NC_000023.9:g.41090594T= NCBI36
NG_012830.1:g.18000T=
NG_012830.2:g.18000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642322.2:c.1616T= ENSP00000496052.2:p.Leu539=
ENST00000399959.7:c.1481T= ENSP00000382840.3:p.Leu494=
ENST00000441189.4:c.1385T= ENSP00000414281.3:p.Leu462=
ENST00000457138.7:c.1436T= ENSP00000392494.2:p.Leu479=
ENST00000611968.2:c.78T=
ENST00000616050.3:c.232T=
ENST00000629496.3:c.1484T= ENSP00000487224.1:p.Leu495=
ENST00000642161.1:n.3683T=
ENST00000642322.1:c.926T= ENSP00000496052.1:p.Leu309=
ENST00000642424.1:c.926T= ENSP00000496356.1:p.Leu309=
ENST00000642589.1:n.4806T=
ENST00000642597.1:n.1658T=
ENST00000642687.1:n.1517T=
ENST00000642722.1:n.2317T=
ENST00000642763.1:n.2375T=
ENST00000642793.1:c.*933T= ENSP00000493976.1:n.*933T=
ENST00000642801.1:n.1133T=
ENST00000643820.1:n.760T=
ENST00000643963.1:c.*766T= ENSP00000495264.1:n.*766T=
ENST00000644073.1:c.1442T= ENSP00000493475.1:p.Leu481=
ENST00000644074.1:c.1481T= ENSP00000496663.1:p.Leu494=
ENST00000644109.1:c.1646T= ENSP00000494952.1:p.Leu549=
ENST00000644307.1:n.1654T=
ENST00000644513.1:c.1484T= ENSP00000493819.1:p.Leu495=
ENST00000644677.1:c.1367T= ENSP00000496524.1:p.Leu456=
ENST00000644876.2:c.1484T= MANE Select ENSP00000494040.1:p.Leu495=
ENST00000644958.1:n.3145T=
ENST00000645080.1:c.*2706T= ENSP00000494767.1:n.*2706T=
ENST00000645120.1:n.2979T=
ENST00000645338.1:n.1654T=
ENST00000645380.1:n.2948T=
ENST00000645561.1:n.2660T=
ENST00000645574.1:n.4348T=
ENST00000645589.1:c.1484T= ENSP00000494588.1:p.Leu495=
ENST00000646107.1:c.1367T= ENSP00000494518.1:p.Leu456=
ENST00000646122.1:c.1484T= ENSP00000496222.1:p.Leu495=
ENST00000646196.1:n.2453T=
ENST00000646223.1:c.*1477T= ENSP00000496043.1:n.*1477T=
ENST00000646319.1:c.1484T= ENSP00000495377.1:p.Leu495=
ENST00000646390.1:n.3772T=
ENST00000646627.1:c.926T= ENSP00000493795.1:p.Leu309=
ENST00000646679.1:c.926T= ENSP00000494887.1:p.Leu309=
ENST00000646822.1:n.2546T=
ENST00000646940.1:n.1658T=
ENST00000647286.1:n.1582T=
ENST00000647477.1:n.223T=
ENST00000399959.6:c.1484T= ENSP00000382840.2:p.Leu495=
ENST00000441189.3:c.341-1243T= ENSP00000414281.2:n.341-1243T=
ENST00000457138.6:c.1436T= ENSP00000392494.2:p.Leu479=
ENST00000478993.5:c.1484T= ENSP00000478443.1:p.Leu495=
ENST00000542215.5:n.1532T=
ENST00000616050.2:c.37T=
ENST00000625837.2:c.1484T= ENSP00000486306.1:p.Leu495=
ENST00000626301.2:c.1484T= ENSP00000486443.1:p.Leu495=
ENST00000629496.2:c.1484T= ENSP00000487224.1:p.Leu495=
ENST00000629785.2:c.1484T= ENSP00000486516.1:p.Leu495=
ENST00000630255.2:c.1484T= ENSP00000486720.1:p.Leu495=
ENST00000630370.2:c.1484T= ENSP00000487062.1:p.Leu495=
ENST00000630858.2:c.1484T= ENSP00000486514.1:p.Leu495=
NM_001193416.2:c.1484T= NP_001180345.1:p.Leu495=
NM_001193417.2:c.1436T= NP_001180346.1:p.Leu479=
NM_001356.4:c.1484T= NP_001347.3:p.Leu495=
NR_126093.1:n.2429T=
XM_011543892.1:c.1484T= XP_011542194.1:p.Leu495=
NM_001363819.1:c.926T= NP_001350748.1:p.Leu309=
XM_011543892.2:c.1484T= XP_011542194.1:p.Leu495=
XM_017029313.1:c.926T= XP_016884802.1:p.Leu309=
NM_001193416.3:c.1484T= NP_001180345.1:p.Leu495=
NM_001193417.3:c.1436T= NP_001180346.1:p.Leu479=
NM_001356.5:c.1484T= MANE Select NP_001347.3:p.Leu495=