Canonical Allele Identifier: CA412776061

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205757G>T (hg19) ; chrX:g.41346504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346504G>T , CM000685.2:g.41346504G>T	GRCh38
NC_000023.10:g.41205757G>T , CM000685.1:g.41205757G>T	GRCh37
NC_000023.9:g.41090701G>T	NCBI36
NG_012830.1:g.18107G>T
NG_012830.2:g.18107G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1630-1G>T	ENSP00000496052.2:n.1630-1G>T
ENST00000399959.7:c.1495-1G>T	ENSP00000382840.3:n.1495-1G>T
ENST00000441189.4:c.1399-1G>T	ENSP00000414281.3:n.1399-1G>T
ENST00000457138.7:c.1450-1G>T	ENSP00000392494.2:n.1450-1G>T
ENST00000611968.2:c.92-1G>T
ENST00000616050.3:c.246-1G>T
ENST00000629496.3:c.1498-1G>T	ENSP00000487224.1:n.1498-1G>T
ENST00000642161.1:n.3697-1G>T
ENST00000642322.1:c.940-1G>T	ENSP00000496052.1:n.940-1G>T
ENST00000642424.1:c.940-1G>T	ENSP00000496356.1:n.940-1G>T
ENST00000642589.1:n.4820-1G>T
ENST00000642597.1:n.1672-1G>T
ENST00000642687.1:n.1531-1G>T
ENST00000642722.1:n.2331-1G>T
ENST00000642763.1:n.2389-1G>T
ENST00000642793.1:c.*947-1G>T	ENSP00000493976.1:n.*947-1G>T
ENST00000642801.1:n.1147-1G>T
ENST00000643820.1:n.867G>T
ENST00000643963.1:c.*780-1G>T	ENSP00000495264.1:n.*780-1G>T
ENST00000644073.1:c.1456-1G>T	ENSP00000493475.1:n.1456-1G>T
ENST00000644074.1:c.1495-1G>T	ENSP00000496663.1:n.1495-1G>T
ENST00000644109.1:c.1660-1G>T	ENSP00000494952.1:n.1660-1G>T
ENST00000644307.1:n.1668-1G>T
ENST00000644513.1:c.1498-1G>T	ENSP00000493819.1:n.1498-1G>T
ENST00000644677.1:c.1381-1G>T	ENSP00000496524.1:n.1381-1G>T
ENST00000644876.2:c.1498-1G>T MANE Select	ENSP00000494040.1:n.1498-1G>T
ENST00000644958.1:n.3159-1G>T
ENST00000645080.1:c.*2720-1G>T	ENSP00000494767.1:n.*2720-1G>T
ENST00000645120.1:n.2993-1G>T
ENST00000645338.1:n.1668-1G>T
ENST00000645380.1:n.2962-1G>T
ENST00000645561.1:n.2674-1G>T
ENST00000645574.1:n.4362-1G>T
ENST00000645589.1:c.1508G>T	ENSP00000494588.1:p.Arg503Met
ENST00000646107.1:c.1381-1G>T	ENSP00000494518.1:n.1381-1G>T
ENST00000646122.1:c.1498-1G>T	ENSP00000496222.1:n.1498-1G>T
ENST00000646196.1:n.2467-1G>T
ENST00000646223.1:c.*1491-1G>T	ENSP00000496043.1:n.*1491-1G>T
ENST00000646319.1:c.1498-1G>T	ENSP00000495377.1:n.1498-1G>T
ENST00000646390.1:n.3786-1G>T
ENST00000646627.1:c.940-1G>T	ENSP00000493795.1:n.940-1G>T
ENST00000646679.1:c.940-1G>T	ENSP00000494887.1:n.940-1G>T
ENST00000646822.1:n.2560-1G>T
ENST00000646940.1:n.1672-1G>T
ENST00000647286.1:n.1596-1G>T
ENST00000647477.1:n.237-1G>T
ENST00000399959.6:c.1498-1G>T	ENSP00000382840.2:n.1498-1G>T
ENST00000441189.3:c.341-1136G>T	ENSP00000414281.2:n.341-1136G>T
ENST00000457138.6:c.1450-1G>T	ENSP00000392494.2:n.1450-1G>T
ENST00000478993.5:c.1498-1G>T	ENSP00000478443.1:n.1498-1G>T
ENST00000542215.5:n.1546-1G>T
ENST00000616050.2:c.51-1G>T
ENST00000625837.2:c.1498-1G>T	ENSP00000486306.1:n.1498-1G>T
ENST00000626301.2:c.1498-1G>T	ENSP00000486443.1:n.1498-1G>T
ENST00000629496.2:c.1498-1G>T	ENSP00000487224.1:n.1498-1G>T
ENST00000629785.2:c.1498-1G>T	ENSP00000486516.1:n.1498-1G>T
ENST00000630255.2:c.1498-1G>T	ENSP00000486720.1:n.1498-1G>T
ENST00000630370.2:c.1498-1G>T	ENSP00000487062.1:n.1498-1G>T
ENST00000630858.2:c.1498-1G>T	ENSP00000486514.1:n.1498-1G>T
NM_001193416.2:c.1498-1G>T	NP_001180345.1:n.1498-1G>T
NM_001193417.2:c.1450-1G>T	NP_001180346.1:n.1450-1G>T
NM_001356.4:c.1498-1G>T	NP_001347.3:n.1498-1G>T
NR_126093.1:n.2443-1G>T
XM_011543892.1:c.1498-1G>T	XP_011542194.1:n.1498-1G>T
NM_001363819.1:c.940-1G>T	NP_001350748.1:n.940-1G>T
XM_011543892.2:c.1498-1G>T	XP_011542194.1:n.1498-1G>T
XM_017029313.1:c.940-1G>T	XP_016884802.1:n.940-1G>T
NM_001193416.3:c.1498-1G>T	NP_001180345.1:n.1498-1G>T
NM_001193417.3:c.1450-1G>T	NP_001180346.1:n.1450-1G>T
NM_001356.5:c.1498-1G>T MANE Select	NP_001347.3:n.1498-1G>T