Canonical Allele Identifier: CA16621383
Gene: DDX3X HGNC NCBI

Linked Data

ClinVar Variation Id: 424139
dbSNP Id: rs1064796820

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41344126A>G , CM000685.2:g.41344126A>G GRCh38
NC_000023.10:g.41203379A>G , CM000685.1:g.41203379A>G GRCh37
NC_000023.9:g.41088323A>G NCBI36
NG_012830.1:g.15729A>G
NG_012830.2:g.15729A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642322.2:c.994A>G ENSP00000496052.2:p.Lys332Glu
ENST00000399959.7:c.859A>G ENSP00000382840.3:p.Lys287Glu
ENST00000441189.4:c.766-113A>G ENSP00000414281.3:n.766-113A>G
ENST00000457138.7:c.814A>G ENSP00000392494.2:p.Lys272Glu
ENST00000629496.3:c.862A>G ENSP00000487224.1:p.Lys288Glu
ENST00000631641.2:n.905A>G
ENST00000642161.1:n.3061A>G
ENST00000642322.1:c.304A>G ENSP00000496052.1:p.Lys102Glu
ENST00000642424.1:c.304A>G ENSP00000496356.1:p.Lys102Glu
ENST00000642589.1:n.4184A>G
ENST00000642597.1:n.1036A>G
ENST00000642687.1:n.895A>G
ENST00000642722.1:n.1695A>G
ENST00000642763.1:n.1753A>G
ENST00000642793.1:c.*311A>G ENSP00000493976.1:n.*311A>G
ENST00000642801.1:n.511A>G
ENST00000643820.1:n.138A>G
ENST00000643963.1:c.*144A>G ENSP00000495264.1:n.*144A>G
ENST00000644073.1:c.820A>G ENSP00000493475.1:p.Lys274Glu
ENST00000644074.1:c.859A>G ENSP00000496663.1:p.Lys287Glu
ENST00000644109.1:c.859A>G ENSP00000494952.1:p.Lys287Glu
ENST00000644307.1:n.953A>G
ENST00000644513.1:c.862A>G ENSP00000493819.1:p.Lys288Glu
ENST00000644677.1:c.745A>G ENSP00000496524.1:p.Lys249Glu
ENST00000644876.2:c.862A>G MANE Select ENSP00000494040.1:p.Lys288Glu
ENST00000644958.1:n.2523A>G
ENST00000645080.1:c.*2084A>G ENSP00000494767.1:n.*2084A>G
ENST00000645120.1:n.2357A>G
ENST00000645338.1:n.953A>G
ENST00000645380.1:n.2247A>G
ENST00000645561.1:n.2038A>G
ENST00000645574.1:n.3726A>G
ENST00000645589.1:c.862A>G ENSP00000494588.1:p.Lys288Glu
ENST00000646107.1:c.745A>G ENSP00000494518.1:p.Lys249Glu
ENST00000646122.1:c.862A>G ENSP00000496222.1:p.Lys288Glu
ENST00000646196.1:n.1831A>G
ENST00000646223.1:c.*855A>G ENSP00000496043.1:n.*855A>G
ENST00000646319.1:c.862A>G ENSP00000495377.1:p.Lys288Glu
ENST00000646390.1:n.3150A>G
ENST00000646627.1:c.304A>G ENSP00000493795.1:p.Lys102Glu
ENST00000646679.1:c.304A>G ENSP00000494887.1:p.Lys102Glu
ENST00000646822.1:n.1924A>G
ENST00000646940.1:n.1036A>G
ENST00000647286.1:n.960A>G
ENST00000399959.6:c.862A>G ENSP00000382840.2:p.Lys288Glu
ENST00000441189.3:c.340+1576A>G ENSP00000414281.2:n.340+1576A>G
ENST00000457138.6:c.814A>G ENSP00000392494.2:p.Lys272Glu
ENST00000478993.5:c.862A>G ENSP00000478443.1:p.Lys288Glu
ENST00000542215.5:n.910A>G
ENST00000625837.2:c.862A>G ENSP00000486306.1:p.Lys288Glu
ENST00000626301.2:c.862A>G ENSP00000486443.1:p.Lys288Glu
ENST00000629496.2:c.862A>G ENSP00000487224.1:p.Lys288Glu
ENST00000629785.2:c.862A>G ENSP00000486516.1:p.Lys288Glu
ENST00000630255.2:c.862A>G ENSP00000486720.1:p.Lys288Glu
ENST00000630370.2:c.862A>G ENSP00000487062.1:p.Lys288Glu
ENST00000630858.2:c.862A>G ENSP00000486514.1:p.Lys288Glu
NM_001193416.2:c.862A>G NP_001180345.1:p.Lys288Glu
NM_001193417.2:c.814A>G NP_001180346.1:p.Lys272Glu
NM_001356.4:c.862A>G NP_001347.3:p.Lys288Glu
NR_126093.1:n.1807A>G
XM_011543892.1:c.862A>G XP_011542194.1:p.Lys288Glu
NM_001363819.1:c.304A>G NP_001350748.1:p.Lys102Glu
XM_011543892.2:c.862A>G XP_011542194.1:p.Lys288Glu
XM_017029313.1:c.304A>G XP_016884802.1:p.Lys102Glu
NM_001193416.3:c.862A>G NP_001180345.1:p.Lys288Glu
NM_001193417.3:c.814A>G NP_001180346.1:p.Lys272Glu
NM_001356.5:c.862A>G MANE Select NP_001347.3:p.Lys288Glu