Canonical Allele Identifier: CA516347462

Gene: DDX3X

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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