Canonical Allele Identifier: CA412776890

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205849G>A (hg19) ; chrX:g.41346596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346596G>A , CM000685.2:g.41346596G>A	GRCh38
NC_000023.10:g.41205849G>A , CM000685.1:g.41205849G>A	GRCh37
NC_000023.9:g.41090793G>A	NCBI36
NG_012830.1:g.18199G>A
NG_012830.2:g.18199G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1721G>A	ENSP00000496052.2:p.Gly574Asp
ENST00000399959.7:c.1586G>A	ENSP00000382840.3:p.Gly529Asp
ENST00000441189.4:c.1490G>A	ENSP00000414281.3:p.Gly497Asp
ENST00000457138.7:c.1541G>A	ENSP00000392494.2:p.Gly514Asp
ENST00000611968.2:c.183G>A
ENST00000616050.3:c.337G>A
ENST00000629496.3:c.1589G>A	ENSP00000487224.1:p.Gly530Asp
ENST00000642161.1:n.3788G>A
ENST00000642322.1:c.1031G>A	ENSP00000496052.1:p.Gly344Asp
ENST00000642424.1:c.1031G>A	ENSP00000496356.1:p.Gly344Asp
ENST00000642589.1:n.4911G>A
ENST00000642597.1:n.1763G>A
ENST00000642687.1:n.1622G>A
ENST00000642722.1:n.2422G>A
ENST00000642763.1:n.2480G>A
ENST00000642793.1:c.*1038G>A	ENSP00000493976.1:n.*1038G>A
ENST00000642801.1:n.1238G>A
ENST00000643820.1:n.959G>A
ENST00000643963.1:c.*871G>A	ENSP00000495264.1:n.*871G>A
ENST00000644073.1:c.1547G>A	ENSP00000493475.1:p.Gly516Asp
ENST00000644074.1:c.1586G>A	ENSP00000496663.1:p.Gly529Asp
ENST00000644109.1:c.1751G>A	ENSP00000494952.1:p.Gly584Asp
ENST00000644307.1:n.1759G>A
ENST00000644513.1:c.1589G>A	ENSP00000493819.1:p.Gly530Asp
ENST00000644677.1:c.1472G>A	ENSP00000496524.1:p.Gly491Asp
ENST00000644876.2:c.1589G>A MANE Select	ENSP00000494040.1:p.Gly530Asp
ENST00000644958.1:n.3250G>A
ENST00000645080.1:c.*2811G>A	ENSP00000494767.1:n.*2811G>A
ENST00000645120.1:n.3084G>A
ENST00000645338.1:n.1759G>A
ENST00000645380.1:n.3053G>A
ENST00000645561.1:n.2765G>A
ENST00000645574.1:n.4453G>A
ENST00000645589.1:c.*88G>A	ENSP00000494588.1:n.*88G>A
ENST00000646107.1:c.1472G>A	ENSP00000494518.1:p.Gly491Asp
ENST00000646122.1:c.1589G>A	ENSP00000496222.1:p.Gly530Asp
ENST00000646196.1:n.2558G>A
ENST00000646223.1:c.*1582G>A	ENSP00000496043.1:n.*1582G>A
ENST00000646319.1:c.1589G>A	ENSP00000495377.1:p.Gly530Asp
ENST00000646390.1:n.3877G>A
ENST00000646627.1:c.1031G>A	ENSP00000493795.1:p.Gly344Asp
ENST00000646679.1:c.1031G>A	ENSP00000494887.1:p.Gly344Asp
ENST00000646822.1:n.2651G>A
ENST00000646940.1:n.1763G>A
ENST00000647286.1:n.1687G>A
ENST00000647477.1:n.328G>A
ENST00000399959.6:c.1589G>A	ENSP00000382840.2:p.Gly530Asp
ENST00000441189.3:c.341-1044G>A	ENSP00000414281.2:n.341-1044G>A
ENST00000457138.6:c.1541G>A	ENSP00000392494.2:p.Gly514Asp
ENST00000478993.5:c.1589G>A	ENSP00000478443.1:p.Gly530Asp
ENST00000611968.1:c.31G>A
ENST00000616050.2:c.142G>A
ENST00000625837.2:c.1589G>A	ENSP00000486306.1:p.Gly530Asp
ENST00000626301.2:c.1589G>A	ENSP00000486443.1:p.Gly530Asp
ENST00000629496.2:c.1589G>A	ENSP00000487224.1:p.Gly530Asp
ENST00000629785.2:c.1589G>A	ENSP00000486516.1:p.Gly530Asp
ENST00000630255.2:c.1589G>A	ENSP00000486720.1:p.Gly530Asp
ENST00000630370.2:c.1589G>A	ENSP00000487062.1:p.Gly530Asp
ENST00000630858.2:c.1589G>A	ENSP00000486514.1:p.Gly530Asp
NM_001193416.2:c.1589G>A	NP_001180345.1:p.Gly530Asp
NM_001193417.2:c.1541G>A	NP_001180346.1:p.Gly514Asp
NM_001356.4:c.1589G>A	NP_001347.3:p.Gly530Asp
NR_126093.1:n.2534G>A
XM_011543892.1:c.1589G>A	XP_011542194.1:p.Gly530Asp
NM_001363819.1:c.1031G>A	NP_001350748.1:p.Gly344Asp
XM_011543892.2:c.1589G>A	XP_011542194.1:p.Gly530Asp
XM_017029313.1:c.1031G>A	XP_016884802.1:p.Gly344Asp
NM_001193416.3:c.1589G>A	NP_001180345.1:p.Gly530Asp
NM_001193417.3:c.1541G>A	NP_001180346.1:p.Gly514Asp
NM_001356.5:c.1589G>A MANE Select	NP_001347.3:p.Gly530Asp