Canonical Allele Identifier: CA412771222

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204434T>G (hg19) ; chrX:g.41345181T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345181T>G , CM000685.2:g.41345181T>G	GRCh38
NC_000023.10:g.41204434T>G , CM000685.1:g.41204434T>G	GRCh37
NC_000023.9:g.41089378T>G	NCBI36
NG_012830.1:g.16784T>G
NG_012830.2:g.16784T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1159T>G	ENSP00000496052.2:p.Tyr387Asp
ENST00000399959.7:c.1024T>G	ENSP00000382840.3:p.Tyr342Asp
ENST00000441189.4:c.928T>G	ENSP00000414281.3:p.Tyr310Asp
ENST00000457138.7:c.979T>G	ENSP00000392494.2:p.Tyr327Asp
ENST00000629496.3:c.1027T>G	ENSP00000487224.1:p.Tyr343Asp
ENST00000642161.1:n.3226T>G
ENST00000642322.1:c.469T>G	ENSP00000496052.1:p.Tyr157Asp
ENST00000642424.1:c.469T>G	ENSP00000496356.1:p.Tyr157Asp
ENST00000642589.1:n.4349T>G
ENST00000642597.1:n.1201T>G
ENST00000642687.1:n.1060T>G
ENST00000642722.1:n.1860T>G
ENST00000642763.1:n.1918T>G
ENST00000642793.1:c.*476T>G	ENSP00000493976.1:n.*476T>G
ENST00000642801.1:n.676T>G
ENST00000643820.1:n.303T>G
ENST00000643963.1:c.*309T>G	ENSP00000495264.1:n.*309T>G
ENST00000644073.1:c.985T>G	ENSP00000493475.1:p.Tyr329Asp
ENST00000644074.1:c.1024T>G	ENSP00000496663.1:p.Tyr342Asp
ENST00000644109.1:c.1189T>G	ENSP00000494952.1:p.Tyr397Asp
ENST00000644307.1:n.1118T>G
ENST00000644513.1:c.1027T>G	ENSP00000493819.1:p.Tyr343Asp
ENST00000644677.1:c.910T>G	ENSP00000496524.1:p.Tyr304Asp
ENST00000644876.2:c.1027T>G MANE Select	ENSP00000494040.1:p.Tyr343Asp
ENST00000644958.1:n.2688T>G
ENST00000645080.1:c.*2249T>G	ENSP00000494767.1:n.*2249T>G
ENST00000645120.1:n.2522T>G
ENST00000645338.1:n.1118T>G
ENST00000645380.1:n.2412T>G
ENST00000645561.1:n.2203T>G
ENST00000645574.1:n.3891T>G
ENST00000645589.1:c.1027T>G	ENSP00000494588.1:p.Tyr343Asp
ENST00000646093.1:n.211T>G
ENST00000646107.1:c.910T>G	ENSP00000494518.1:p.Tyr304Asp
ENST00000646122.1:c.1027T>G	ENSP00000496222.1:p.Tyr343Asp
ENST00000646196.1:n.1996T>G
ENST00000646223.1:c.*1020T>G	ENSP00000496043.1:n.*1020T>G
ENST00000646319.1:c.1027T>G	ENSP00000495377.1:p.Tyr343Asp
ENST00000646390.1:n.3315T>G
ENST00000646627.1:c.469T>G	ENSP00000493795.1:p.Tyr157Asp
ENST00000646679.1:c.469T>G	ENSP00000494887.1:p.Tyr157Asp
ENST00000646822.1:n.2089T>G
ENST00000646940.1:n.1201T>G
ENST00000647286.1:n.1125T>G
ENST00000399959.6:c.1027T>G	ENSP00000382840.2:p.Tyr343Asp
ENST00000441189.3:c.341-2459T>G	ENSP00000414281.2:n.341-2459T>G
ENST00000457138.6:c.979T>G	ENSP00000392494.2:p.Tyr327Asp
ENST00000478993.5:c.1027T>G	ENSP00000478443.1:p.Tyr343Asp
ENST00000542215.5:n.1075T>G
ENST00000625837.2:c.1027T>G	ENSP00000486306.1:p.Tyr343Asp
ENST00000626301.2:c.1027T>G	ENSP00000486443.1:p.Tyr343Asp
ENST00000629496.2:c.1027T>G	ENSP00000487224.1:p.Tyr343Asp
ENST00000629785.2:c.1027T>G	ENSP00000486516.1:p.Tyr343Asp
ENST00000630255.2:c.1027T>G	ENSP00000486720.1:p.Tyr343Asp
ENST00000630370.2:c.1027T>G	ENSP00000487062.1:p.Tyr343Asp
ENST00000630858.2:c.1027T>G	ENSP00000486514.1:p.Tyr343Asp
NM_001193416.2:c.1027T>G	NP_001180345.1:p.Tyr343Asp
NM_001193417.2:c.979T>G	NP_001180346.1:p.Tyr327Asp
NM_001356.4:c.1027T>G	NP_001347.3:p.Tyr343Asp
NR_126093.1:n.1972T>G
XM_011543892.1:c.1027T>G	XP_011542194.1:p.Tyr343Asp
NM_001363819.1:c.469T>G	NP_001350748.1:p.Tyr157Asp
XM_011543892.2:c.1027T>G	XP_011542194.1:p.Tyr343Asp
XM_017029313.1:c.469T>G	XP_016884802.1:p.Tyr157Asp
NM_001193416.3:c.1027T>G	NP_001180345.1:p.Tyr343Asp
NM_001193417.3:c.979T>G	NP_001180346.1:p.Tyr327Asp
NM_001356.5:c.1027T>G MANE Select	NP_001347.3:p.Tyr343Asp