Canonical Allele Identifier: CA412773930

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205481G>T (hg19) ; chrX:g.41346228G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346228G>T , CM000685.2:g.41346228G>T	GRCh38
NC_000023.10:g.41205481G>T , CM000685.1:g.41205481G>T	GRCh37
NC_000023.9:g.41090425G>T	NCBI36
NG_012830.1:g.17831G>T
NG_012830.2:g.17831G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1448-1G>T	ENSP00000496052.2:n.1448-1G>T
ENST00000399959.7:c.1313-1G>T	ENSP00000382840.3:n.1313-1G>T
ENST00000441189.4:c.1217-1G>T	ENSP00000414281.3:n.1217-1G>T
ENST00000457138.7:c.1268-1G>T	ENSP00000392494.2:n.1268-1G>T
ENST00000616050.3:c.64-1G>T
ENST00000629496.3:c.1316-1G>T	ENSP00000487224.1:n.1316-1G>T
ENST00000642161.1:n.3515-1G>T
ENST00000642322.1:c.758-1G>T	ENSP00000496052.1:n.758-1G>T
ENST00000642424.1:c.758-1G>T	ENSP00000496356.1:n.758-1G>T
ENST00000642589.1:n.4638-1G>T
ENST00000642597.1:n.1490-1G>T
ENST00000642687.1:n.1349-1G>T
ENST00000642722.1:n.2149-1G>T
ENST00000642763.1:n.2207-1G>T
ENST00000642793.1:c.*765-1G>T	ENSP00000493976.1:n.*765-1G>T
ENST00000642801.1:n.965-1G>T
ENST00000643820.1:n.592-1G>T
ENST00000643963.1:c.*598-1G>T	ENSP00000495264.1:n.*598-1G>T
ENST00000644073.1:c.1274-1G>T	ENSP00000493475.1:n.1274-1G>T
ENST00000644074.1:c.1313-1G>T	ENSP00000496663.1:n.1313-1G>T
ENST00000644109.1:c.1478-1G>T	ENSP00000494952.1:n.1478-1G>T
ENST00000644307.1:n.1486-1G>T
ENST00000644513.1:c.1316-1G>T	ENSP00000493819.1:n.1316-1G>T
ENST00000644677.1:c.1199-1G>T	ENSP00000496524.1:n.1199-1G>T
ENST00000644876.2:c.1316-1G>T MANE Select	ENSP00000494040.1:n.1316-1G>T
ENST00000644958.1:n.2977-1G>T
ENST00000645080.1:c.*2538-1G>T	ENSP00000494767.1:n.*2538-1G>T
ENST00000645120.1:n.2811-1G>T
ENST00000645338.1:n.1486-1G>T
ENST00000645380.1:n.2780-1G>T
ENST00000645561.1:n.2492-1G>T
ENST00000645574.1:n.4180-1G>T
ENST00000645589.1:c.1316-1G>T	ENSP00000494588.1:n.1316-1G>T
ENST00000646093.1:n.500-1G>T
ENST00000646107.1:c.1199-1G>T	ENSP00000494518.1:n.1199-1G>T
ENST00000646122.1:c.1316-1G>T	ENSP00000496222.1:n.1316-1G>T
ENST00000646196.1:n.2285-1G>T
ENST00000646223.1:c.*1309-1G>T	ENSP00000496043.1:n.*1309-1G>T
ENST00000646319.1:c.1316-1G>T	ENSP00000495377.1:n.1316-1G>T
ENST00000646390.1:n.3604-1G>T
ENST00000646627.1:c.758-1G>T	ENSP00000493795.1:n.758-1G>T
ENST00000646679.1:c.758-1G>T	ENSP00000494887.1:n.758-1G>T
ENST00000646822.1:n.2378-1G>T
ENST00000646940.1:n.1490-1G>T
ENST00000647286.1:n.1414-1G>T
ENST00000647477.1:n.55-1G>T
ENST00000399959.6:c.1316-1G>T	ENSP00000382840.2:n.1316-1G>T
ENST00000441189.3:c.341-1412G>T	ENSP00000414281.2:n.341-1412G>T
ENST00000457138.6:c.1268-1G>T	ENSP00000392494.2:n.1268-1G>T
ENST00000478993.5:c.1316-1G>T	ENSP00000478443.1:n.1316-1G>T
ENST00000542215.5:n.1364-1G>T
ENST00000625837.2:c.1316-1G>T	ENSP00000486306.1:n.1316-1G>T
ENST00000626301.2:c.1316-1G>T	ENSP00000486443.1:n.1316-1G>T
ENST00000629496.2:c.1316-1G>T	ENSP00000487224.1:n.1316-1G>T
ENST00000629785.2:c.1316-1G>T	ENSP00000486516.1:n.1316-1G>T
ENST00000630255.2:c.1316-1G>T	ENSP00000486720.1:n.1316-1G>T
ENST00000630370.2:c.1316-1G>T	ENSP00000487062.1:n.1316-1G>T
ENST00000630858.2:c.1316-1G>T	ENSP00000486514.1:n.1316-1G>T
NM_001193416.2:c.1316-1G>T	NP_001180345.1:n.1316-1G>T
NM_001193417.2:c.1268-1G>T	NP_001180346.1:n.1268-1G>T
NM_001356.4:c.1316-1G>T	NP_001347.3:n.1316-1G>T
NR_126093.1:n.2261-1G>T
XM_011543892.1:c.1316-1G>T	XP_011542194.1:n.1316-1G>T
NM_001363819.1:c.758-1G>T	NP_001350748.1:n.758-1G>T
XM_011543892.2:c.1316-1G>T	XP_011542194.1:n.1316-1G>T
XM_017029313.1:c.758-1G>T	XP_016884802.1:n.758-1G>T
NM_001193416.3:c.1316-1G>T	NP_001180345.1:n.1316-1G>T
NM_001193417.3:c.1268-1G>T	NP_001180346.1:n.1268-1G>T
NM_001356.5:c.1316-1G>T MANE Select	NP_001347.3:n.1316-1G>T