Canonical Allele Identifier: CA516347461

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205865A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346612A>C , CM000685.2:g.41346612A>C	GRCh38
NC_000023.10:g.41205865A>C , CM000685.1:g.41205865A>C	GRCh37
NC_000023.9:g.41090809A>C	NCBI36
NG_012830.1:g.18215A>C
NG_012830.2:g.18215A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1737A>C	ENSP00000496052.2:p.Val579=
ENST00000399959.7:c.1602A>C	ENSP00000382840.3:p.Val534=
ENST00000441189.4:c.1506A>C	ENSP00000414281.3:p.Val502=
ENST00000457138.7:c.1557A>C	ENSP00000392494.2:p.Val519=
ENST00000611968.2:c.199A>C
ENST00000616050.3:c.353A>C
ENST00000629496.3:c.1605A>C	ENSP00000487224.1:p.Val535=
ENST00000642161.1:n.3804A>C
ENST00000642322.1:c.1047A>C	ENSP00000496052.1:p.Val349=
ENST00000642424.1:c.1047A>C	ENSP00000496356.1:p.Val349=
ENST00000642589.1:n.4927A>C
ENST00000642597.1:n.1779A>C
ENST00000642687.1:n.1638A>C
ENST00000642722.1:n.2438A>C
ENST00000642763.1:n.2496A>C
ENST00000642793.1:c.*1054A>C	ENSP00000493976.1:n.*1054A>C
ENST00000642801.1:n.1254A>C
ENST00000643820.1:n.975A>C
ENST00000643963.1:c.*887A>C	ENSP00000495264.1:n.*887A>C
ENST00000644073.1:c.1563A>C	ENSP00000493475.1:p.Val521=
ENST00000644074.1:c.1602A>C	ENSP00000496663.1:p.Val534=
ENST00000644109.1:c.1767A>C	ENSP00000494952.1:p.Val589=
ENST00000644307.1:n.1775A>C
ENST00000644513.1:c.1605A>C	ENSP00000493819.1:p.Val535=
ENST00000644677.1:c.1488A>C	ENSP00000496524.1:p.Val496=
ENST00000644876.2:c.1605A>C MANE Select	ENSP00000494040.1:p.Val535=
ENST00000644958.1:n.3266A>C
ENST00000645080.1:c.*2827A>C	ENSP00000494767.1:n.*2827A>C
ENST00000645120.1:n.3100A>C
ENST00000645338.1:n.1775A>C
ENST00000645380.1:n.3069A>C
ENST00000645561.1:n.2781A>C
ENST00000645574.1:n.4469A>C
ENST00000645589.1:c.*104A>C	ENSP00000494588.1:n.*104A>C
ENST00000646107.1:c.1488A>C	ENSP00000494518.1:p.Val496=
ENST00000646122.1:c.1605A>C	ENSP00000496222.1:p.Val535=
ENST00000646196.1:n.2574A>C
ENST00000646223.1:c.*1598A>C	ENSP00000496043.1:n.*1598A>C
ENST00000646319.1:c.1605A>C	ENSP00000495377.1:p.Val535=
ENST00000646390.1:n.3893A>C
ENST00000646627.1:c.1047A>C	ENSP00000493795.1:p.Val349=
ENST00000646679.1:c.1047A>C	ENSP00000494887.1:p.Val349=
ENST00000646822.1:n.2667A>C
ENST00000646940.1:n.1779A>C
ENST00000647286.1:n.1703A>C
ENST00000647477.1:n.344A>C
ENST00000399959.6:c.1605A>C	ENSP00000382840.2:p.Val535=
ENST00000441189.3:c.341-1028A>C	ENSP00000414281.2:n.341-1028A>C
ENST00000457138.6:c.1557A>C	ENSP00000392494.2:p.Val519=
ENST00000478993.5:c.1605A>C	ENSP00000478443.1:p.Val535=
ENST00000611968.1:c.47A>C
ENST00000616050.2:c.158A>C
ENST00000625837.2:c.1605A>C	ENSP00000486306.1:p.Val535=
ENST00000626301.2:c.1605A>C	ENSP00000486443.1:p.Val535=
ENST00000629496.2:c.1605A>C	ENSP00000487224.1:p.Val535=
ENST00000629785.2:c.1605A>C	ENSP00000486516.1:p.Val535=
ENST00000630255.2:c.1605A>C	ENSP00000486720.1:p.Val535=
ENST00000630370.2:c.1605A>C	ENSP00000487062.1:p.Val535=
ENST00000630858.2:c.1605A>C	ENSP00000486514.1:p.Val535=
NM_001193416.2:c.1605A>C	NP_001180345.1:p.Val535=
NM_001193417.2:c.1557A>C	NP_001180346.1:p.Val519=
NM_001356.4:c.1605A>C	NP_001347.3:p.Val535=
NR_126093.1:n.2550A>C
XM_011543892.1:c.1605A>C	XP_011542194.1:p.Val535=
NM_001363819.1:c.1047A>C	NP_001350748.1:p.Val349=
XM_011543892.2:c.1605A>C	XP_011542194.1:p.Val535=
XM_017029313.1:c.1047A>C	XP_016884802.1:p.Val349=
NM_001193416.3:c.1605A>C	NP_001180345.1:p.Val535=
NM_001193417.3:c.1557A>C	NP_001180346.1:p.Val519=
NM_001356.5:c.1605A>C MANE Select	NP_001347.3:p.Val535=