Canonical Allele Identifier: CA412776334

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205794C>G (hg19) ; chrX:g.41346541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346541C>G , CM000685.2:g.41346541C>G	GRCh38
NC_000023.10:g.41205794C>G , CM000685.1:g.41205794C>G	GRCh37
NC_000023.9:g.41090738C>G	NCBI36
NG_012830.1:g.18144C>G
NG_012830.2:g.18144C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1666C>G	ENSP00000496052.2:p.His556Asp
ENST00000399959.7:c.1531C>G	ENSP00000382840.3:p.His511Asp
ENST00000441189.4:c.1435C>G	ENSP00000414281.3:p.His479Asp
ENST00000457138.7:c.1486C>G	ENSP00000392494.2:p.His496Asp
ENST00000611968.2:c.128C>G
ENST00000616050.3:c.282C>G
ENST00000629496.3:c.1534C>G	ENSP00000487224.1:p.His512Asp
ENST00000642161.1:n.3733C>G
ENST00000642322.1:c.976C>G	ENSP00000496052.1:p.His326Asp
ENST00000642424.1:c.976C>G	ENSP00000496356.1:p.His326Asp
ENST00000642589.1:n.4856C>G
ENST00000642597.1:n.1708C>G
ENST00000642687.1:n.1567C>G
ENST00000642722.1:n.2367C>G
ENST00000642763.1:n.2425C>G
ENST00000642793.1:c.*983C>G	ENSP00000493976.1:n.*983C>G
ENST00000642801.1:n.1183C>G
ENST00000643820.1:n.904C>G
ENST00000643963.1:c.*816C>G	ENSP00000495264.1:n.*816C>G
ENST00000644073.1:c.1492C>G	ENSP00000493475.1:p.His498Asp
ENST00000644074.1:c.1531C>G	ENSP00000496663.1:p.His511Asp
ENST00000644109.1:c.1696C>G	ENSP00000494952.1:p.His566Asp
ENST00000644307.1:n.1704C>G
ENST00000644513.1:c.1534C>G	ENSP00000493819.1:p.His512Asp
ENST00000644677.1:c.1417C>G	ENSP00000496524.1:p.His473Asp
ENST00000644876.2:c.1534C>G MANE Select	ENSP00000494040.1:p.His512Asp
ENST00000644958.1:n.3195C>G
ENST00000645080.1:c.*2756C>G	ENSP00000494767.1:n.*2756C>G
ENST00000645120.1:n.3029C>G
ENST00000645338.1:n.1704C>G
ENST00000645380.1:n.2998C>G
ENST00000645561.1:n.2710C>G
ENST00000645574.1:n.4398C>G
ENST00000645589.1:c.*33C>G	ENSP00000494588.1:n.*33C>G
ENST00000646107.1:c.1417C>G	ENSP00000494518.1:p.His473Asp
ENST00000646122.1:c.1534C>G	ENSP00000496222.1:p.His512Asp
ENST00000646196.1:n.2503C>G
ENST00000646223.1:c.*1527C>G	ENSP00000496043.1:n.*1527C>G
ENST00000646319.1:c.1534C>G	ENSP00000495377.1:p.His512Asp
ENST00000646390.1:n.3822C>G
ENST00000646627.1:c.976C>G	ENSP00000493795.1:p.His326Asp
ENST00000646679.1:c.976C>G	ENSP00000494887.1:p.His326Asp
ENST00000646822.1:n.2596C>G
ENST00000646940.1:n.1708C>G
ENST00000647286.1:n.1632C>G
ENST00000647477.1:n.273C>G
ENST00000399959.6:c.1534C>G	ENSP00000382840.2:p.His512Asp
ENST00000441189.3:c.341-1099C>G	ENSP00000414281.2:n.341-1099C>G
ENST00000457138.6:c.1486C>G	ENSP00000392494.2:p.His496Asp
ENST00000478993.5:c.1534C>G	ENSP00000478443.1:p.His512Asp
ENST00000542215.5:n.1582C>G
ENST00000616050.2:c.87C>G
ENST00000625837.2:c.1534C>G	ENSP00000486306.1:p.His512Asp
ENST00000626301.2:c.1534C>G	ENSP00000486443.1:p.His512Asp
ENST00000629496.2:c.1534C>G	ENSP00000487224.1:p.His512Asp
ENST00000629785.2:c.1534C>G	ENSP00000486516.1:p.His512Asp
ENST00000630255.2:c.1534C>G	ENSP00000486720.1:p.His512Asp
ENST00000630370.2:c.1534C>G	ENSP00000487062.1:p.His512Asp
ENST00000630858.2:c.1534C>G	ENSP00000486514.1:p.His512Asp
NM_001193416.2:c.1534C>G	NP_001180345.1:p.His512Asp
NM_001193417.2:c.1486C>G	NP_001180346.1:p.His496Asp
NM_001356.4:c.1534C>G	NP_001347.3:p.His512Asp
NR_126093.1:n.2479C>G
XM_011543892.1:c.1534C>G	XP_011542194.1:p.His512Asp
NM_001363819.1:c.976C>G	NP_001350748.1:p.His326Asp
XM_011543892.2:c.1534C>G	XP_011542194.1:p.His512Asp
XM_017029313.1:c.976C>G	XP_016884802.1:p.His326Asp
NM_001193416.3:c.1534C>G	NP_001180345.1:p.His512Asp
NM_001193417.3:c.1486C>G	NP_001180346.1:p.His496Asp
NM_001356.5:c.1534C>G MANE Select	NP_001347.3:p.His512Asp