Canonical Allele Identifier: CA412776909

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205851C>T (hg19) ; chrX:g.41346598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346598C>T , CM000685.2:g.41346598C>T	GRCh38
NC_000023.10:g.41205851C>T , CM000685.1:g.41205851C>T	GRCh37
NC_000023.9:g.41090795C>T	NCBI36
NG_012830.1:g.18201C>T
NG_012830.2:g.18201C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1723C>T	ENSP00000496052.2:p.Arg575Cys
ENST00000399959.7:c.1588C>T	ENSP00000382840.3:p.Arg530Cys
ENST00000441189.4:c.1492C>T	ENSP00000414281.3:p.Arg498Cys
ENST00000457138.7:c.1543C>T	ENSP00000392494.2:p.Arg515Cys
ENST00000611968.2:c.185C>T
ENST00000616050.3:c.339C>T
ENST00000629496.3:c.1591C>T	ENSP00000487224.1:p.Arg531Cys
ENST00000642161.1:n.3790C>T
ENST00000642322.1:c.1033C>T	ENSP00000496052.1:p.Arg345Cys
ENST00000642424.1:c.1033C>T	ENSP00000496356.1:p.Arg345Cys
ENST00000642589.1:n.4913C>T
ENST00000642597.1:n.1765C>T
ENST00000642687.1:n.1624C>T
ENST00000642722.1:n.2424C>T
ENST00000642763.1:n.2482C>T
ENST00000642793.1:c.*1040C>T	ENSP00000493976.1:n.*1040C>T
ENST00000642801.1:n.1240C>T
ENST00000643820.1:n.961C>T
ENST00000643963.1:c.*873C>T	ENSP00000495264.1:n.*873C>T
ENST00000644073.1:c.1549C>T	ENSP00000493475.1:p.Arg517Cys
ENST00000644074.1:c.1588C>T	ENSP00000496663.1:p.Arg530Cys
ENST00000644109.1:c.1753C>T	ENSP00000494952.1:p.Arg585Cys
ENST00000644307.1:n.1761C>T
ENST00000644513.1:c.1591C>T	ENSP00000493819.1:p.Arg531Cys
ENST00000644677.1:c.1474C>T	ENSP00000496524.1:p.Arg492Cys
ENST00000644876.2:c.1591C>T MANE Select	ENSP00000494040.1:p.Arg531Cys
ENST00000644958.1:n.3252C>T
ENST00000645080.1:c.*2813C>T	ENSP00000494767.1:n.*2813C>T
ENST00000645120.1:n.3086C>T
ENST00000645338.1:n.1761C>T
ENST00000645380.1:n.3055C>T
ENST00000645561.1:n.2767C>T
ENST00000645574.1:n.4455C>T
ENST00000645589.1:c.*90C>T	ENSP00000494588.1:n.*90C>T
ENST00000646107.1:c.1474C>T	ENSP00000494518.1:p.Arg492Cys
ENST00000646122.1:c.1591C>T	ENSP00000496222.1:p.Arg531Cys
ENST00000646196.1:n.2560C>T
ENST00000646223.1:c.*1584C>T	ENSP00000496043.1:n.*1584C>T
ENST00000646319.1:c.1591C>T	ENSP00000495377.1:p.Arg531Cys
ENST00000646390.1:n.3879C>T
ENST00000646627.1:c.1033C>T	ENSP00000493795.1:p.Arg345Cys
ENST00000646679.1:c.1033C>T	ENSP00000494887.1:p.Arg345Cys
ENST00000646822.1:n.2653C>T
ENST00000646940.1:n.1765C>T
ENST00000647286.1:n.1689C>T
ENST00000647477.1:n.330C>T
ENST00000399959.6:c.1591C>T	ENSP00000382840.2:p.Arg531Cys
ENST00000441189.3:c.341-1042C>T	ENSP00000414281.2:n.341-1042C>T
ENST00000457138.6:c.1543C>T	ENSP00000392494.2:p.Arg515Cys
ENST00000478993.5:c.1591C>T	ENSP00000478443.1:p.Arg531Cys
ENST00000611968.1:c.33C>T
ENST00000616050.2:c.144C>T
ENST00000625837.2:c.1591C>T	ENSP00000486306.1:p.Arg531Cys
ENST00000626301.2:c.1591C>T	ENSP00000486443.1:p.Arg531Cys
ENST00000629496.2:c.1591C>T	ENSP00000487224.1:p.Arg531Cys
ENST00000629785.2:c.1591C>T	ENSP00000486516.1:p.Arg531Cys
ENST00000630255.2:c.1591C>T	ENSP00000486720.1:p.Arg531Cys
ENST00000630370.2:c.1591C>T	ENSP00000487062.1:p.Arg531Cys
ENST00000630858.2:c.1591C>T	ENSP00000486514.1:p.Arg531Cys
NM_001193416.2:c.1591C>T	NP_001180345.1:p.Arg531Cys
NM_001193417.2:c.1543C>T	NP_001180346.1:p.Arg515Cys
NM_001356.4:c.1591C>T	NP_001347.3:p.Arg531Cys
NR_126093.1:n.2536C>T
XM_011543892.1:c.1591C>T	XP_011542194.1:p.Arg531Cys
NM_001363819.1:c.1033C>T	NP_001350748.1:p.Arg345Cys
XM_011543892.2:c.1591C>T	XP_011542194.1:p.Arg531Cys
XM_017029313.1:c.1033C>T	XP_016884802.1:p.Arg345Cys
NM_001193416.3:c.1591C>T	NP_001180345.1:p.Arg531Cys
NM_001193417.3:c.1543C>T	NP_001180346.1:p.Arg515Cys
NM_001356.5:c.1591C>T MANE Select	NP_001347.3:p.Arg531Cys