Canonical Allele Identifier: CA2425880596

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344317C= , CM000685.2:g.41344317C=	GRCh38
NC_000023.10:g.41203570C= , CM000685.1:g.41203570C=	GRCh37
NC_000023.9:g.41088514C=	NCBI36
NG_012830.1:g.15920C=
NG_012830.2:g.15920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1075C=	ENSP00000496052.2:p.Arg359=
ENST00000399959.7:c.940C=	ENSP00000382840.3:p.Arg314=
ENST00000441189.4:c.844C=	ENSP00000414281.3:p.Arg282=
ENST00000457138.7:c.895C=	ENSP00000392494.2:p.Arg299=
ENST00000629496.3:c.943C=	ENSP00000487224.1:p.Arg315=
ENST00000631641.2:n.986C=
ENST00000642161.1:n.3142C=
ENST00000642322.1:c.385C=	ENSP00000496052.1:p.Arg129=
ENST00000642424.1:c.385C=	ENSP00000496356.1:p.Arg129=
ENST00000642589.1:n.4265C=
ENST00000642597.1:n.1117C=
ENST00000642687.1:n.976C=
ENST00000642722.1:n.1776C=
ENST00000642763.1:n.1834C=
ENST00000642793.1:c.*392C=	ENSP00000493976.1:n.*392C=
ENST00000642801.1:n.592C=
ENST00000643820.1:n.219C=
ENST00000643963.1:c.*225C=	ENSP00000495264.1:n.*225C=
ENST00000644073.1:c.901C=	ENSP00000493475.1:p.Arg301=
ENST00000644074.1:c.940C=	ENSP00000496663.1:p.Arg314=
ENST00000644109.1:c.940C=	ENSP00000494952.1:p.Arg314=
ENST00000644307.1:n.1034C=
ENST00000644513.1:c.943C=	ENSP00000493819.1:p.Arg315=
ENST00000644677.1:c.826C=	ENSP00000496524.1:p.Arg276=
ENST00000644876.2:c.943C= MANE Select	ENSP00000494040.1:p.Arg315=
ENST00000644958.1:n.2604C=
ENST00000645080.1:c.*2165C=	ENSP00000494767.1:n.*2165C=
ENST00000645120.1:n.2438C=
ENST00000645338.1:n.1034C=
ENST00000645380.1:n.2328C=
ENST00000645561.1:n.2119C=
ENST00000645574.1:n.3807C=
ENST00000645589.1:c.943C=	ENSP00000494588.1:p.Arg315=
ENST00000646093.1:n.127C=
ENST00000646107.1:c.826C=	ENSP00000494518.1:p.Arg276=
ENST00000646122.1:c.943C=	ENSP00000496222.1:p.Arg315=
ENST00000646196.1:n.1912C=
ENST00000646223.1:c.*936C=	ENSP00000496043.1:n.*936C=
ENST00000646319.1:c.943C=	ENSP00000495377.1:p.Arg315=
ENST00000646390.1:n.3231C=
ENST00000646627.1:c.385C=	ENSP00000493795.1:p.Arg129=
ENST00000646679.1:c.385C=	ENSP00000494887.1:p.Arg129=
ENST00000646822.1:n.2005C=
ENST00000646940.1:n.1117C=
ENST00000647286.1:n.1041C=
ENST00000399959.6:c.943C=	ENSP00000382840.2:p.Arg315=
ENST00000441189.3:c.340+1767C=	ENSP00000414281.2:n.340+1767C=
ENST00000457138.6:c.895C=	ENSP00000392494.2:p.Arg299=
ENST00000478993.5:c.943C=	ENSP00000478443.1:p.Arg315=
ENST00000542215.5:n.991C=
ENST00000625837.2:c.943C=	ENSP00000486306.1:p.Arg315=
ENST00000626301.2:c.943C=	ENSP00000486443.1:p.Arg315=
ENST00000629496.2:c.943C=	ENSP00000487224.1:p.Arg315=
ENST00000629785.2:c.943C=	ENSP00000486516.1:p.Arg315=
ENST00000630255.2:c.943C=	ENSP00000486720.1:p.Arg315=
ENST00000630370.2:c.943C=	ENSP00000487062.1:p.Arg315=
ENST00000630858.2:c.943C=	ENSP00000486514.1:p.Arg315=
NM_001193416.2:c.943C=	NP_001180345.1:p.Arg315=
NM_001193417.2:c.895C=	NP_001180346.1:p.Arg299=
NM_001356.4:c.943C=	NP_001347.3:p.Arg315=
NR_126093.1:n.1888C=
XM_011543892.1:c.943C=	XP_011542194.1:p.Arg315=
NM_001363819.1:c.385C=	NP_001350748.1:p.Arg129=
XM_011543892.2:c.943C=	XP_011542194.1:p.Arg315=
XM_017029313.1:c.385C=	XP_016884802.1:p.Arg129=
NM_001193416.3:c.943C=	NP_001180345.1:p.Arg315=
NM_001193417.3:c.895C=	NP_001180346.1:p.Arg299=
NM_001356.5:c.943C= MANE Select	NP_001347.3:p.Arg315=