Canonical Allele Identifier: CA412776801

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205839C>G (hg19) ; chrX:g.41346586C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346586C>G , CM000685.2:g.41346586C>G	GRCh38
NC_000023.10:g.41205839C>G , CM000685.1:g.41205839C>G	GRCh37
NC_000023.9:g.41090783C>G	NCBI36
NG_012830.1:g.18189C>G
NG_012830.2:g.18189C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1711C>G	ENSP00000496052.2:p.His571Asp
ENST00000399959.7:c.1576C>G	ENSP00000382840.3:p.His526Asp
ENST00000441189.4:c.1480C>G	ENSP00000414281.3:p.His494Asp
ENST00000457138.7:c.1531C>G	ENSP00000392494.2:p.His511Asp
ENST00000611968.2:c.173C>G
ENST00000616050.3:c.327C>G
ENST00000629496.3:c.1579C>G	ENSP00000487224.1:p.His527Asp
ENST00000642161.1:n.3778C>G
ENST00000642322.1:c.1021C>G	ENSP00000496052.1:p.His341Asp
ENST00000642424.1:c.1021C>G	ENSP00000496356.1:p.His341Asp
ENST00000642589.1:n.4901C>G
ENST00000642597.1:n.1753C>G
ENST00000642687.1:n.1612C>G
ENST00000642722.1:n.2412C>G
ENST00000642763.1:n.2470C>G
ENST00000642793.1:c.*1028C>G	ENSP00000493976.1:n.*1028C>G
ENST00000642801.1:n.1228C>G
ENST00000643820.1:n.949C>G
ENST00000643963.1:c.*861C>G	ENSP00000495264.1:n.*861C>G
ENST00000644073.1:c.1537C>G	ENSP00000493475.1:p.His513Asp
ENST00000644074.1:c.1576C>G	ENSP00000496663.1:p.His526Asp
ENST00000644109.1:c.1741C>G	ENSP00000494952.1:p.His581Asp
ENST00000644307.1:n.1749C>G
ENST00000644513.1:c.1579C>G	ENSP00000493819.1:p.His527Asp
ENST00000644677.1:c.1462C>G	ENSP00000496524.1:p.His488Asp
ENST00000644876.2:c.1579C>G MANE Select	ENSP00000494040.1:p.His527Asp
ENST00000644958.1:n.3240C>G
ENST00000645080.1:c.*2801C>G	ENSP00000494767.1:n.*2801C>G
ENST00000645120.1:n.3074C>G
ENST00000645338.1:n.1749C>G
ENST00000645380.1:n.3043C>G
ENST00000645561.1:n.2755C>G
ENST00000645574.1:n.4443C>G
ENST00000645589.1:c.*78C>G	ENSP00000494588.1:n.*78C>G
ENST00000646107.1:c.1462C>G	ENSP00000494518.1:p.His488Asp
ENST00000646122.1:c.1579C>G	ENSP00000496222.1:p.His527Asp
ENST00000646196.1:n.2548C>G
ENST00000646223.1:c.*1572C>G	ENSP00000496043.1:n.*1572C>G
ENST00000646319.1:c.1579C>G	ENSP00000495377.1:p.His527Asp
ENST00000646390.1:n.3867C>G
ENST00000646627.1:c.1021C>G	ENSP00000493795.1:p.His341Asp
ENST00000646679.1:c.1021C>G	ENSP00000494887.1:p.His341Asp
ENST00000646822.1:n.2641C>G
ENST00000646940.1:n.1753C>G
ENST00000647286.1:n.1677C>G
ENST00000647477.1:n.318C>G
ENST00000399959.6:c.1579C>G	ENSP00000382840.2:p.His527Asp
ENST00000441189.3:c.341-1054C>G	ENSP00000414281.2:n.341-1054C>G
ENST00000457138.6:c.1531C>G	ENSP00000392494.2:p.His511Asp
ENST00000478993.5:c.1579C>G	ENSP00000478443.1:p.His527Asp
ENST00000611968.1:c.21C>G
ENST00000616050.2:c.132C>G
ENST00000625837.2:c.1579C>G	ENSP00000486306.1:p.His527Asp
ENST00000626301.2:c.1579C>G	ENSP00000486443.1:p.His527Asp
ENST00000629496.2:c.1579C>G	ENSP00000487224.1:p.His527Asp
ENST00000629785.2:c.1579C>G	ENSP00000486516.1:p.His527Asp
ENST00000630255.2:c.1579C>G	ENSP00000486720.1:p.His527Asp
ENST00000630370.2:c.1579C>G	ENSP00000487062.1:p.His527Asp
ENST00000630858.2:c.1579C>G	ENSP00000486514.1:p.His527Asp
NM_001193416.2:c.1579C>G	NP_001180345.1:p.His527Asp
NM_001193417.2:c.1531C>G	NP_001180346.1:p.His511Asp
NM_001356.4:c.1579C>G	NP_001347.3:p.His527Asp
NR_126093.1:n.2524C>G
XM_011543892.1:c.1579C>G	XP_011542194.1:p.His527Asp
NM_001363819.1:c.1021C>G	NP_001350748.1:p.His341Asp
XM_011543892.2:c.1579C>G	XP_011542194.1:p.His527Asp
XM_017029313.1:c.1021C>G	XP_016884802.1:p.His341Asp
NM_001193416.3:c.1579C>G	NP_001180345.1:p.His527Asp
NM_001193417.3:c.1531C>G	NP_001180346.1:p.His511Asp
NM_001356.5:c.1579C>G MANE Select	NP_001347.3:p.His527Asp