Canonical Allele Identifier: CA515972500

Gene: DDX3X

Linked Data

• dbSNP Id: rs1271216981
• MyVariant Identifiers: chrX:g.41205597G>A (hg19) ; chrX:g.41346344G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346344G>A , CM000685.2:g.41346344G>A	GRCh38
NC_000023.10:g.41205597G>A , CM000685.1:g.41205597G>A	GRCh37
NC_000023.9:g.41090541G>A	NCBI36
NG_012830.1:g.17947G>A
NG_012830.2:g.17947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1563G>A	ENSP00000496052.2:p.Gln521=
ENST00000399959.7:c.1428G>A	ENSP00000382840.3:p.Gln476=
ENST00000441189.4:c.1332G>A	ENSP00000414281.3:p.Gln444=
ENST00000457138.7:c.1383G>A	ENSP00000392494.2:p.Gln461=
ENST00000611968.2:c.25G>A
ENST00000616050.3:c.179G>A
ENST00000629496.3:c.1431G>A	ENSP00000487224.1:p.Gln477=
ENST00000642161.1:n.3630G>A
ENST00000642322.1:c.873G>A	ENSP00000496052.1:p.Gln291=
ENST00000642424.1:c.873G>A	ENSP00000496356.1:p.Gln291=
ENST00000642589.1:n.4753G>A
ENST00000642597.1:n.1605G>A
ENST00000642687.1:n.1464G>A
ENST00000642722.1:n.2264G>A
ENST00000642763.1:n.2322G>A
ENST00000642793.1:c.*880G>A	ENSP00000493976.1:n.*880G>A
ENST00000642801.1:n.1080G>A
ENST00000643820.1:n.707G>A
ENST00000643963.1:c.*713G>A	ENSP00000495264.1:n.*713G>A
ENST00000644073.1:c.1389G>A	ENSP00000493475.1:p.Gln463=
ENST00000644074.1:c.1428G>A	ENSP00000496663.1:p.Gln476=
ENST00000644109.1:c.1593G>A	ENSP00000494952.1:p.Gln531=
ENST00000644307.1:n.1601G>A
ENST00000644513.1:c.1431G>A	ENSP00000493819.1:p.Gln477=
ENST00000644677.1:c.1314G>A	ENSP00000496524.1:p.Gln438=
ENST00000644876.2:c.1431G>A MANE Select	ENSP00000494040.1:p.Gln477=
ENST00000644958.1:n.3092G>A
ENST00000645080.1:c.*2653G>A	ENSP00000494767.1:n.*2653G>A
ENST00000645120.1:n.2926G>A
ENST00000645338.1:n.1601G>A
ENST00000645380.1:n.2895G>A
ENST00000645561.1:n.2607G>A
ENST00000645574.1:n.4295G>A
ENST00000645589.1:c.1431G>A	ENSP00000494588.1:p.Gln477=
ENST00000646107.1:c.1314G>A	ENSP00000494518.1:p.Gln438=
ENST00000646122.1:c.1431G>A	ENSP00000496222.1:p.Gln477=
ENST00000646196.1:n.2400G>A
ENST00000646223.1:c.*1424G>A	ENSP00000496043.1:n.*1424G>A
ENST00000646319.1:c.1431G>A	ENSP00000495377.1:p.Gln477=
ENST00000646390.1:n.3719G>A
ENST00000646627.1:c.873G>A	ENSP00000493795.1:p.Gln291=
ENST00000646679.1:c.873G>A	ENSP00000494887.1:p.Gln291=
ENST00000646822.1:n.2493G>A
ENST00000646940.1:n.1605G>A
ENST00000647286.1:n.1529G>A
ENST00000647477.1:n.170G>A
ENST00000399959.6:c.1431G>A	ENSP00000382840.2:p.Gln477=
ENST00000441189.3:c.341-1296G>A	ENSP00000414281.2:n.341-1296G>A
ENST00000457138.6:c.1383G>A	ENSP00000392494.2:p.Gln461=
ENST00000478993.5:c.1431G>A	ENSP00000478443.1:p.Gln477=
ENST00000542215.5:n.1479G>A
ENST00000625837.2:c.1431G>A	ENSP00000486306.1:p.Gln477=
ENST00000626301.2:c.1431G>A	ENSP00000486443.1:p.Gln477=
ENST00000629496.2:c.1431G>A	ENSP00000487224.1:p.Gln477=
ENST00000629785.2:c.1431G>A	ENSP00000486516.1:p.Gln477=
ENST00000630255.2:c.1431G>A	ENSP00000486720.1:p.Gln477=
ENST00000630370.2:c.1431G>A	ENSP00000487062.1:p.Gln477=
ENST00000630858.2:c.1431G>A	ENSP00000486514.1:p.Gln477=
NM_001193416.2:c.1431G>A	NP_001180345.1:p.Gln477=
NM_001193417.2:c.1383G>A	NP_001180346.1:p.Gln461=
NM_001356.4:c.1431G>A	NP_001347.3:p.Gln477=
NR_126093.1:n.2376G>A
XM_011543892.1:c.1431G>A	XP_011542194.1:p.Gln477=
NM_001363819.1:c.873G>A	NP_001350748.1:p.Gln291=
XM_011543892.2:c.1431G>A	XP_011542194.1:p.Gln477=
XM_017029313.1:c.873G>A	XP_016884802.1:p.Gln291=
NM_001193416.3:c.1431G>A	NP_001180345.1:p.Gln477=
NM_001193417.3:c.1383G>A	NP_001180346.1:p.Gln461=
NM_001356.5:c.1431G>A MANE Select	NP_001347.3:p.Gln477=