Canonical Allele Identifier: CA2579588566

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346463T>C , CM000685.2:g.41346463T>C	GRCh38
NC_000023.10:g.41205716T>C , CM000685.1:g.41205716T>C	GRCh37
NC_000023.9:g.41090660T>C	NCBI36
NG_012830.1:g.18066T>C
NG_012830.2:g.18066T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1630-42T>C	ENSP00000496052.2:n.1630-42T>C
ENST00000399959.7:c.1495-42T>C	ENSP00000382840.3:n.1495-42T>C
ENST00000441189.4:c.1399-42T>C	ENSP00000414281.3:n.1399-42T>C
ENST00000457138.7:c.1450-42T>C	ENSP00000392494.2:n.1450-42T>C
ENST00000611968.2:c.92-42T>C
ENST00000616050.3:c.246-42T>C
ENST00000629496.3:c.1498-42T>C	ENSP00000487224.1:n.1498-42T>C
ENST00000642161.1:n.3697-42T>C
ENST00000642322.1:c.940-42T>C	ENSP00000496052.1:n.940-42T>C
ENST00000642424.1:c.940-42T>C	ENSP00000496356.1:n.940-42T>C
ENST00000642589.1:n.4820-42T>C
ENST00000642597.1:n.1672-42T>C
ENST00000642687.1:n.1531-42T>C
ENST00000642722.1:n.2331-42T>C
ENST00000642763.1:n.2389-42T>C
ENST00000642793.1:c.*947-42T>C	ENSP00000493976.1:n.*947-42T>C
ENST00000642801.1:n.1147-42T>C
ENST00000643820.1:n.826T>C
ENST00000643963.1:c.*780-42T>C	ENSP00000495264.1:n.*780-42T>C
ENST00000644073.1:c.1456-42T>C	ENSP00000493475.1:n.1456-42T>C
ENST00000644074.1:c.1495-42T>C	ENSP00000496663.1:n.1495-42T>C
ENST00000644109.1:c.1660-42T>C	ENSP00000494952.1:n.1660-42T>C
ENST00000644307.1:n.1668-42T>C
ENST00000644513.1:c.1498-42T>C	ENSP00000493819.1:n.1498-42T>C
ENST00000644677.1:c.1381-42T>C	ENSP00000496524.1:n.1381-42T>C
ENST00000644876.2:c.1498-42T>C MANE Select	ENSP00000494040.1:n.1498-42T>C
ENST00000644958.1:n.3159-42T>C
ENST00000645080.1:c.*2720-42T>C	ENSP00000494767.1:n.*2720-42T>C
ENST00000645120.1:n.2993-42T>C
ENST00000645338.1:n.1668-42T>C
ENST00000645380.1:n.2962-42T>C
ENST00000645561.1:n.2674-42T>C
ENST00000645574.1:n.4362-42T>C
ENST00000645589.1:c.1498-31T>C	ENSP00000494588.1:n.1498-31T>C
ENST00000646107.1:c.1381-42T>C	ENSP00000494518.1:n.1381-42T>C
ENST00000646122.1:c.1498-42T>C	ENSP00000496222.1:n.1498-42T>C
ENST00000646196.1:n.2467-42T>C
ENST00000646223.1:c.*1491-42T>C	ENSP00000496043.1:n.*1491-42T>C
ENST00000646319.1:c.1498-42T>C	ENSP00000495377.1:n.1498-42T>C
ENST00000646390.1:n.3786-42T>C
ENST00000646627.1:c.940-42T>C	ENSP00000493795.1:n.940-42T>C
ENST00000646679.1:c.940-42T>C	ENSP00000494887.1:n.940-42T>C
ENST00000646822.1:n.2560-42T>C
ENST00000646940.1:n.1672-42T>C
ENST00000647286.1:n.1596-42T>C
ENST00000647477.1:n.237-42T>C
ENST00000399959.6:c.1498-42T>C	ENSP00000382840.2:n.1498-42T>C
ENST00000441189.3:c.341-1177T>C	ENSP00000414281.2:n.341-1177T>C
ENST00000457138.6:c.1450-42T>C	ENSP00000392494.2:n.1450-42T>C
ENST00000478993.5:c.1498-42T>C	ENSP00000478443.1:n.1498-42T>C
ENST00000542215.5:n.1546-42T>C
ENST00000616050.2:c.51-42T>C
ENST00000625837.2:c.1498-42T>C	ENSP00000486306.1:n.1498-42T>C
ENST00000626301.2:c.1498-42T>C	ENSP00000486443.1:n.1498-42T>C
ENST00000629496.2:c.1498-42T>C	ENSP00000487224.1:n.1498-42T>C
ENST00000629785.2:c.1498-42T>C	ENSP00000486516.1:n.1498-42T>C
ENST00000630255.2:c.1498-42T>C	ENSP00000486720.1:n.1498-42T>C
ENST00000630370.2:c.1498-42T>C	ENSP00000487062.1:n.1498-42T>C
ENST00000630858.2:c.1498-42T>C	ENSP00000486514.1:n.1498-42T>C
NM_001193416.2:c.1498-42T>C	NP_001180345.1:n.1498-42T>C
NM_001193417.2:c.1450-42T>C	NP_001180346.1:n.1450-42T>C
NM_001356.4:c.1498-42T>C	NP_001347.3:n.1498-42T>C
NR_126093.1:n.2443-42T>C
XM_011543892.1:c.1498-42T>C	XP_011542194.1:n.1498-42T>C
NM_001363819.1:c.940-42T>C	NP_001350748.1:n.940-42T>C
XM_011543892.2:c.1498-42T>C	XP_011542194.1:n.1498-42T>C
XM_017029313.1:c.940-42T>C	XP_016884802.1:n.940-42T>C
NM_001193416.3:c.1498-42T>C	NP_001180345.1:n.1498-42T>C
NM_001193417.3:c.1450-42T>C	NP_001180346.1:n.1450-42T>C
NM_001356.5:c.1498-42T>C MANE Select	NP_001347.3:n.1498-42T>C