Canonical Allele Identifier: CA516347308

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41203507A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344254A>C , CM000685.2:g.41344254A>C	GRCh38
NC_000023.10:g.41203507A>C , CM000685.1:g.41203507A>C	GRCh37
NC_000023.9:g.41088451A>C	NCBI36
NG_012830.1:g.15857A>C
NG_012830.2:g.15857A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1012A>C	ENSP00000496052.2:p.Arg338=
ENST00000399959.7:c.877A>C	ENSP00000382840.3:p.Arg293=
ENST00000441189.4:c.781A>C	ENSP00000414281.3:p.Arg261=
ENST00000457138.7:c.832A>C	ENSP00000392494.2:p.Arg278=
ENST00000629496.3:c.880A>C	ENSP00000487224.1:p.Arg294=
ENST00000631641.2:n.923A>C
ENST00000642161.1:n.3079A>C
ENST00000642322.1:c.322A>C	ENSP00000496052.1:p.Arg108=
ENST00000642424.1:c.322A>C	ENSP00000496356.1:p.Arg108=
ENST00000642589.1:n.4202A>C
ENST00000642597.1:n.1054A>C
ENST00000642687.1:n.913A>C
ENST00000642722.1:n.1713A>C
ENST00000642763.1:n.1771A>C
ENST00000642793.1:c.*329A>C	ENSP00000493976.1:n.*329A>C
ENST00000642801.1:n.529A>C
ENST00000643820.1:n.156A>C
ENST00000643963.1:c.*162A>C	ENSP00000495264.1:n.*162A>C
ENST00000644073.1:c.838A>C	ENSP00000493475.1:p.Arg280=
ENST00000644074.1:c.877A>C	ENSP00000496663.1:p.Arg293=
ENST00000644109.1:c.877A>C	ENSP00000494952.1:p.Arg293=
ENST00000644307.1:n.971A>C
ENST00000644513.1:c.880A>C	ENSP00000493819.1:p.Arg294=
ENST00000644677.1:c.763A>C	ENSP00000496524.1:p.Arg255=
ENST00000644876.2:c.880A>C MANE Select	ENSP00000494040.1:p.Arg294=
ENST00000644958.1:n.2541A>C
ENST00000645080.1:c.*2102A>C	ENSP00000494767.1:n.*2102A>C
ENST00000645120.1:n.2375A>C
ENST00000645338.1:n.971A>C
ENST00000645380.1:n.2265A>C
ENST00000645561.1:n.2056A>C
ENST00000645574.1:n.3744A>C
ENST00000645589.1:c.880A>C	ENSP00000494588.1:p.Arg294=
ENST00000646093.1:n.64A>C
ENST00000646107.1:c.763A>C	ENSP00000494518.1:p.Arg255=
ENST00000646122.1:c.880A>C	ENSP00000496222.1:p.Arg294=
ENST00000646196.1:n.1849A>C
ENST00000646223.1:c.*873A>C	ENSP00000496043.1:n.*873A>C
ENST00000646319.1:c.880A>C	ENSP00000495377.1:p.Arg294=
ENST00000646390.1:n.3168A>C
ENST00000646627.1:c.322A>C	ENSP00000493795.1:p.Arg108=
ENST00000646679.1:c.322A>C	ENSP00000494887.1:p.Arg108=
ENST00000646822.1:n.1942A>C
ENST00000646940.1:n.1054A>C
ENST00000647286.1:n.978A>C
ENST00000399959.6:c.880A>C	ENSP00000382840.2:p.Arg294=
ENST00000441189.3:c.340+1704A>C	ENSP00000414281.2:n.340+1704A>C
ENST00000457138.6:c.832A>C	ENSP00000392494.2:p.Arg278=
ENST00000478993.5:c.880A>C	ENSP00000478443.1:p.Arg294=
ENST00000542215.5:n.928A>C
ENST00000625837.2:c.880A>C	ENSP00000486306.1:p.Arg294=
ENST00000626301.2:c.880A>C	ENSP00000486443.1:p.Arg294=
ENST00000629496.2:c.880A>C	ENSP00000487224.1:p.Arg294=
ENST00000629785.2:c.880A>C	ENSP00000486516.1:p.Arg294=
ENST00000630255.2:c.880A>C	ENSP00000486720.1:p.Arg294=
ENST00000630370.2:c.880A>C	ENSP00000487062.1:p.Arg294=
ENST00000630858.2:c.880A>C	ENSP00000486514.1:p.Arg294=
NM_001193416.2:c.880A>C	NP_001180345.1:p.Arg294=
NM_001193417.2:c.832A>C	NP_001180346.1:p.Arg278=
NM_001356.4:c.880A>C	NP_001347.3:p.Arg294=
NR_126093.1:n.1825A>C
XM_011543892.1:c.880A>C	XP_011542194.1:p.Arg294=
NM_001363819.1:c.322A>C	NP_001350748.1:p.Arg108=
XM_011543892.2:c.880A>C	XP_011542194.1:p.Arg294=
XM_017029313.1:c.322A>C	XP_016884802.1:p.Arg108=
NM_001193416.3:c.880A>C	NP_001180345.1:p.Arg294=
NM_001193417.3:c.832A>C	NP_001180346.1:p.Arg278=
NM_001356.5:c.880A>C MANE Select	NP_001347.3:p.Arg294=