Canonical Allele Identifier: CA2425881501

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346579A= , CM000685.2:g.41346579A=	GRCh38
NC_000023.10:g.41205832A= , CM000685.1:g.41205832A=	GRCh37
NC_000023.9:g.41090776A=	NCBI36
NG_012830.1:g.18182A=
NG_012830.2:g.18182A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1704A=	ENSP00000496052.2:p.Glu568=
ENST00000399959.7:c.1569A=	ENSP00000382840.3:p.Glu523=
ENST00000441189.4:c.1473A=	ENSP00000414281.3:p.Glu491=
ENST00000457138.7:c.1524A=	ENSP00000392494.2:p.Glu508=
ENST00000611968.2:c.166A=
ENST00000616050.3:c.320A=
ENST00000629496.3:c.1572A=	ENSP00000487224.1:p.Glu524=
ENST00000642161.1:n.3771A=
ENST00000642322.1:c.1014A=	ENSP00000496052.1:p.Glu338=
ENST00000642424.1:c.1014A=	ENSP00000496356.1:p.Glu338=
ENST00000642589.1:n.4894A=
ENST00000642597.1:n.1746A=
ENST00000642687.1:n.1605A=
ENST00000642722.1:n.2405A=
ENST00000642763.1:n.2463A=
ENST00000642793.1:c.*1021A=	ENSP00000493976.1:n.*1021A=
ENST00000642801.1:n.1221A=
ENST00000643820.1:n.942A=
ENST00000643963.1:c.*854A=	ENSP00000495264.1:n.*854A=
ENST00000644073.1:c.1530A=	ENSP00000493475.1:p.Glu510=
ENST00000644074.1:c.1569A=	ENSP00000496663.1:p.Glu523=
ENST00000644109.1:c.1734A=	ENSP00000494952.1:p.Glu578=
ENST00000644307.1:n.1742A=
ENST00000644513.1:c.1572A=	ENSP00000493819.1:p.Glu524=
ENST00000644677.1:c.1455A=	ENSP00000496524.1:p.Glu485=
ENST00000644876.2:c.1572A= MANE Select	ENSP00000494040.1:p.Glu524=
ENST00000644958.1:n.3233A=
ENST00000645080.1:c.*2794A=	ENSP00000494767.1:n.*2794A=
ENST00000645120.1:n.3067A=
ENST00000645338.1:n.1742A=
ENST00000645380.1:n.3036A=
ENST00000645561.1:n.2748A=
ENST00000645574.1:n.4436A=
ENST00000645589.1:c.*71A=	ENSP00000494588.1:n.*71A=
ENST00000646107.1:c.1455A=	ENSP00000494518.1:p.Glu485=
ENST00000646122.1:c.1572A=	ENSP00000496222.1:p.Glu524=
ENST00000646196.1:n.2541A=
ENST00000646223.1:c.*1565A=	ENSP00000496043.1:n.*1565A=
ENST00000646319.1:c.1572A=	ENSP00000495377.1:p.Glu524=
ENST00000646390.1:n.3860A=
ENST00000646627.1:c.1014A=	ENSP00000493795.1:p.Glu338=
ENST00000646679.1:c.1014A=	ENSP00000494887.1:p.Glu338=
ENST00000646822.1:n.2634A=
ENST00000646940.1:n.1746A=
ENST00000647286.1:n.1670A=
ENST00000647477.1:n.311A=
ENST00000399959.6:c.1572A=	ENSP00000382840.2:p.Glu524=
ENST00000441189.3:c.341-1061A=	ENSP00000414281.2:n.341-1061A=
ENST00000457138.6:c.1524A=	ENSP00000392494.2:p.Glu508=
ENST00000478993.5:c.1572A=	ENSP00000478443.1:p.Glu524=
ENST00000611968.1:c.14A=
ENST00000616050.2:c.125A=
ENST00000625837.2:c.1572A=	ENSP00000486306.1:p.Glu524=
ENST00000626301.2:c.1572A=	ENSP00000486443.1:p.Glu524=
ENST00000629496.2:c.1572A=	ENSP00000487224.1:p.Glu524=
ENST00000629785.2:c.1572A=	ENSP00000486516.1:p.Glu524=
ENST00000630255.2:c.1572A=	ENSP00000486720.1:p.Glu524=
ENST00000630370.2:c.1572A=	ENSP00000487062.1:p.Glu524=
ENST00000630858.2:c.1572A=	ENSP00000486514.1:p.Glu524=
NM_001193416.2:c.1572A=	NP_001180345.1:p.Glu524=
NM_001193417.2:c.1524A=	NP_001180346.1:p.Glu508=
NM_001356.4:c.1572A=	NP_001347.3:p.Glu524=
NR_126093.1:n.2517A=
XM_011543892.1:c.1572A=	XP_011542194.1:p.Glu524=
NM_001363819.1:c.1014A=	NP_001350748.1:p.Glu338=
XM_011543892.2:c.1572A=	XP_011542194.1:p.Glu524=
XM_017029313.1:c.1014A=	XP_016884802.1:p.Glu338=
NM_001193416.3:c.1572A=	NP_001180345.1:p.Glu524=
NM_001193417.3:c.1524A=	NP_001180346.1:p.Glu508=
NM_001356.5:c.1572A= MANE Select	NP_001347.3:p.Glu524=