Canonical Allele Identifier: CA412770599

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41203498T>G (hg19) ; chrX:g.41344245T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344245T>G , CM000685.2:g.41344245T>G	GRCh38
NC_000023.10:g.41203498T>G , CM000685.1:g.41203498T>G	GRCh37
NC_000023.9:g.41088442T>G	NCBI36
NG_012830.1:g.15848T>G
NG_012830.2:g.15848T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1003T>G	ENSP00000496052.2:p.Tyr335Asp
ENST00000399959.7:c.868T>G	ENSP00000382840.3:p.Tyr290Asp
ENST00000441189.4:c.772T>G	ENSP00000414281.3:p.Tyr258Asp
ENST00000457138.7:c.823T>G	ENSP00000392494.2:p.Tyr275Asp
ENST00000629496.3:c.871T>G	ENSP00000487224.1:p.Tyr291Asp
ENST00000631641.2:n.914T>G
ENST00000642161.1:n.3070T>G
ENST00000642322.1:c.313T>G	ENSP00000496052.1:p.Tyr105Asp
ENST00000642424.1:c.313T>G	ENSP00000496356.1:p.Tyr105Asp
ENST00000642589.1:n.4193T>G
ENST00000642597.1:n.1045T>G
ENST00000642687.1:n.904T>G
ENST00000642722.1:n.1704T>G
ENST00000642763.1:n.1762T>G
ENST00000642793.1:c.*320T>G	ENSP00000493976.1:n.*320T>G
ENST00000642801.1:n.520T>G
ENST00000643820.1:n.147T>G
ENST00000643963.1:c.*153T>G	ENSP00000495264.1:n.*153T>G
ENST00000644073.1:c.829T>G	ENSP00000493475.1:p.Tyr277Asp
ENST00000644074.1:c.868T>G	ENSP00000496663.1:p.Tyr290Asp
ENST00000644109.1:c.868T>G	ENSP00000494952.1:p.Tyr290Asp
ENST00000644307.1:n.962T>G
ENST00000644513.1:c.871T>G	ENSP00000493819.1:p.Tyr291Asp
ENST00000644677.1:c.754T>G	ENSP00000496524.1:p.Tyr252Asp
ENST00000644876.2:c.871T>G MANE Select	ENSP00000494040.1:p.Tyr291Asp
ENST00000644958.1:n.2532T>G
ENST00000645080.1:c.*2093T>G	ENSP00000494767.1:n.*2093T>G
ENST00000645120.1:n.2366T>G
ENST00000645338.1:n.962T>G
ENST00000645380.1:n.2256T>G
ENST00000645561.1:n.2047T>G
ENST00000645574.1:n.3735T>G
ENST00000645589.1:c.871T>G	ENSP00000494588.1:p.Tyr291Asp
ENST00000646093.1:n.55T>G
ENST00000646107.1:c.754T>G	ENSP00000494518.1:p.Tyr252Asp
ENST00000646122.1:c.871T>G	ENSP00000496222.1:p.Tyr291Asp
ENST00000646196.1:n.1840T>G
ENST00000646223.1:c.*864T>G	ENSP00000496043.1:n.*864T>G
ENST00000646319.1:c.871T>G	ENSP00000495377.1:p.Tyr291Asp
ENST00000646390.1:n.3159T>G
ENST00000646627.1:c.313T>G	ENSP00000493795.1:p.Tyr105Asp
ENST00000646679.1:c.313T>G	ENSP00000494887.1:p.Tyr105Asp
ENST00000646822.1:n.1933T>G
ENST00000646940.1:n.1045T>G
ENST00000647286.1:n.969T>G
ENST00000399959.6:c.871T>G	ENSP00000382840.2:p.Tyr291Asp
ENST00000441189.3:c.340+1695T>G	ENSP00000414281.2:n.340+1695T>G
ENST00000457138.6:c.823T>G	ENSP00000392494.2:p.Tyr275Asp
ENST00000478993.5:c.871T>G	ENSP00000478443.1:p.Tyr291Asp
ENST00000542215.5:n.919T>G
ENST00000625837.2:c.871T>G	ENSP00000486306.1:p.Tyr291Asp
ENST00000626301.2:c.871T>G	ENSP00000486443.1:p.Tyr291Asp
ENST00000629496.2:c.871T>G	ENSP00000487224.1:p.Tyr291Asp
ENST00000629785.2:c.871T>G	ENSP00000486516.1:p.Tyr291Asp
ENST00000630255.2:c.871T>G	ENSP00000486720.1:p.Tyr291Asp
ENST00000630370.2:c.871T>G	ENSP00000487062.1:p.Tyr291Asp
ENST00000630858.2:c.871T>G	ENSP00000486514.1:p.Tyr291Asp
NM_001193416.2:c.871T>G	NP_001180345.1:p.Tyr291Asp
NM_001193417.2:c.823T>G	NP_001180346.1:p.Tyr275Asp
NM_001356.4:c.871T>G	NP_001347.3:p.Tyr291Asp
NR_126093.1:n.1816T>G
XM_011543892.1:c.871T>G	XP_011542194.1:p.Tyr291Asp
NM_001363819.1:c.313T>G	NP_001350748.1:p.Tyr105Asp
XM_011543892.2:c.871T>G	XP_011542194.1:p.Tyr291Asp
XM_017029313.1:c.313T>G	XP_016884802.1:p.Tyr105Asp
NM_001193416.3:c.871T>G	NP_001180345.1:p.Tyr291Asp
NM_001193417.3:c.823T>G	NP_001180346.1:p.Tyr275Asp
NM_001356.5:c.871T>G MANE Select	NP_001347.3:p.Tyr291Asp