Canonical Allele Identifier: CA2425881493

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346545T= , CM000685.2:g.41346545T=	GRCh38
NC_000023.10:g.41205798T= , CM000685.1:g.41205798T=	GRCh37
NC_000023.9:g.41090742T=	NCBI36
NG_012830.1:g.18148T=
NG_012830.2:g.18148T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1670T=	ENSP00000496052.2:p.Val557=
ENST00000399959.7:c.1535T=	ENSP00000382840.3:p.Val512=
ENST00000441189.4:c.1439T=	ENSP00000414281.3:p.Val480=
ENST00000457138.7:c.1490T=	ENSP00000392494.2:p.Val497=
ENST00000611968.2:c.132T=
ENST00000616050.3:c.286T=
ENST00000629496.3:c.1538T=	ENSP00000487224.1:p.Val513=
ENST00000642161.1:n.3737T=
ENST00000642322.1:c.980T=	ENSP00000496052.1:p.Val327=
ENST00000642424.1:c.980T=	ENSP00000496356.1:p.Val327=
ENST00000642589.1:n.4860T=
ENST00000642597.1:n.1712T=
ENST00000642687.1:n.1571T=
ENST00000642722.1:n.2371T=
ENST00000642763.1:n.2429T=
ENST00000642793.1:c.*987T=	ENSP00000493976.1:n.*987T=
ENST00000642801.1:n.1187T=
ENST00000643820.1:n.908T=
ENST00000643963.1:c.*820T=	ENSP00000495264.1:n.*820T=
ENST00000644073.1:c.1496T=	ENSP00000493475.1:p.Val499=
ENST00000644074.1:c.1535T=	ENSP00000496663.1:p.Val512=
ENST00000644109.1:c.1700T=	ENSP00000494952.1:p.Val567=
ENST00000644307.1:n.1708T=
ENST00000644513.1:c.1538T=	ENSP00000493819.1:p.Val513=
ENST00000644677.1:c.1421T=	ENSP00000496524.1:p.Val474=
ENST00000644876.2:c.1538T= MANE Select	ENSP00000494040.1:p.Val513=
ENST00000644958.1:n.3199T=
ENST00000645080.1:c.*2760T=	ENSP00000494767.1:n.*2760T=
ENST00000645120.1:n.3033T=
ENST00000645338.1:n.1708T=
ENST00000645380.1:n.3002T=
ENST00000645561.1:n.2714T=
ENST00000645574.1:n.4402T=
ENST00000645589.1:c.*37T=	ENSP00000494588.1:n.*37T=
ENST00000646107.1:c.1421T=	ENSP00000494518.1:p.Val474=
ENST00000646122.1:c.1538T=	ENSP00000496222.1:p.Val513=
ENST00000646196.1:n.2507T=
ENST00000646223.1:c.*1531T=	ENSP00000496043.1:n.*1531T=
ENST00000646319.1:c.1538T=	ENSP00000495377.1:p.Val513=
ENST00000646390.1:n.3826T=
ENST00000646627.1:c.980T=	ENSP00000493795.1:p.Val327=
ENST00000646679.1:c.980T=	ENSP00000494887.1:p.Val327=
ENST00000646822.1:n.2600T=
ENST00000646940.1:n.1712T=
ENST00000647286.1:n.1636T=
ENST00000647477.1:n.277T=
ENST00000399959.6:c.1538T=	ENSP00000382840.2:p.Val513=
ENST00000441189.3:c.341-1095T=	ENSP00000414281.2:n.341-1095T=
ENST00000457138.6:c.1490T=	ENSP00000392494.2:p.Val497=
ENST00000478993.5:c.1538T=	ENSP00000478443.1:p.Val513=
ENST00000542215.5:n.1586T=
ENST00000616050.2:c.91T=
ENST00000625837.2:c.1538T=	ENSP00000486306.1:p.Val513=
ENST00000626301.2:c.1538T=	ENSP00000486443.1:p.Val513=
ENST00000629496.2:c.1538T=	ENSP00000487224.1:p.Val513=
ENST00000629785.2:c.1538T=	ENSP00000486516.1:p.Val513=
ENST00000630255.2:c.1538T=	ENSP00000486720.1:p.Val513=
ENST00000630370.2:c.1538T=	ENSP00000487062.1:p.Val513=
ENST00000630858.2:c.1538T=	ENSP00000486514.1:p.Val513=
NM_001193416.2:c.1538T=	NP_001180345.1:p.Val513=
NM_001193417.2:c.1490T=	NP_001180346.1:p.Val497=
NM_001356.4:c.1538T=	NP_001347.3:p.Val513=
NR_126093.1:n.2483T=
XM_011543892.1:c.1538T=	XP_011542194.1:p.Val513=
NM_001363819.1:c.980T=	NP_001350748.1:p.Val327=
XM_011543892.2:c.1538T=	XP_011542194.1:p.Val513=
XM_017029313.1:c.980T=	XP_016884802.1:p.Val327=
NM_001193416.3:c.1538T=	NP_001180345.1:p.Val513=
NM_001193417.3:c.1490T=	NP_001180346.1:p.Val497=
NM_001356.5:c.1538T= MANE Select	NP_001347.3:p.Val513=