Canonical Allele Identifier: CA412771311

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204471T>G (hg19) ; chrX:g.41345218T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345218T>G , CM000685.2:g.41345218T>G	GRCh38
NC_000023.10:g.41204471T>G , CM000685.1:g.41204471T>G	GRCh37
NC_000023.9:g.41089415T>G	NCBI36
NG_012830.1:g.16821T>G
NG_012830.2:g.16821T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1196T>G	ENSP00000496052.2:p.Met399Arg
ENST00000399959.7:c.1061T>G	ENSP00000382840.3:p.Met354Arg
ENST00000441189.4:c.965T>G	ENSP00000414281.3:p.Met322Arg
ENST00000457138.7:c.1016T>G	ENSP00000392494.2:p.Met339Arg
ENST00000629496.3:c.1064T>G	ENSP00000487224.1:p.Met355Arg
ENST00000642161.1:n.3263T>G
ENST00000642322.1:c.506T>G	ENSP00000496052.1:p.Met169Arg
ENST00000642424.1:c.506T>G	ENSP00000496356.1:p.Met169Arg
ENST00000642589.1:n.4386T>G
ENST00000642597.1:n.1238T>G
ENST00000642687.1:n.1097T>G
ENST00000642722.1:n.1897T>G
ENST00000642763.1:n.1955T>G
ENST00000642793.1:c.*513T>G	ENSP00000493976.1:n.*513T>G
ENST00000642801.1:n.713T>G
ENST00000643820.1:n.340T>G
ENST00000643963.1:c.*346T>G	ENSP00000495264.1:n.*346T>G
ENST00000644073.1:c.1022T>G	ENSP00000493475.1:p.Met341Arg
ENST00000644074.1:c.1061T>G	ENSP00000496663.1:p.Met354Arg
ENST00000644109.1:c.1226T>G	ENSP00000494952.1:p.Met409Arg
ENST00000644307.1:n.1155T>G
ENST00000644513.1:c.1064T>G	ENSP00000493819.1:p.Met355Arg
ENST00000644677.1:c.947T>G	ENSP00000496524.1:p.Met316Arg
ENST00000644876.2:c.1064T>G MANE Select	ENSP00000494040.1:p.Met355Arg
ENST00000644958.1:n.2725T>G
ENST00000645080.1:c.*2286T>G	ENSP00000494767.1:n.*2286T>G
ENST00000645120.1:n.2559T>G
ENST00000645338.1:n.1155T>G
ENST00000645380.1:n.2449T>G
ENST00000645561.1:n.2240T>G
ENST00000645574.1:n.3928T>G
ENST00000645589.1:c.1064T>G	ENSP00000494588.1:p.Met355Arg
ENST00000646093.1:n.248T>G
ENST00000646107.1:c.947T>G	ENSP00000494518.1:p.Met316Arg
ENST00000646122.1:c.1064T>G	ENSP00000496222.1:p.Met355Arg
ENST00000646196.1:n.2033T>G
ENST00000646223.1:c.*1057T>G	ENSP00000496043.1:n.*1057T>G
ENST00000646319.1:c.1064T>G	ENSP00000495377.1:p.Met355Arg
ENST00000646390.1:n.3352T>G
ENST00000646627.1:c.506T>G	ENSP00000493795.1:p.Met169Arg
ENST00000646679.1:c.506T>G	ENSP00000494887.1:p.Met169Arg
ENST00000646822.1:n.2126T>G
ENST00000646940.1:n.1238T>G
ENST00000647286.1:n.1162T>G
ENST00000399959.6:c.1064T>G	ENSP00000382840.2:p.Met355Arg
ENST00000441189.3:c.341-2422T>G	ENSP00000414281.2:n.341-2422T>G
ENST00000457138.6:c.1016T>G	ENSP00000392494.2:p.Met339Arg
ENST00000478993.5:c.1064T>G	ENSP00000478443.1:p.Met355Arg
ENST00000542215.5:n.1112T>G
ENST00000625837.2:c.1064T>G	ENSP00000486306.1:p.Met355Arg
ENST00000626301.2:c.1064T>G	ENSP00000486443.1:p.Met355Arg
ENST00000629496.2:c.1064T>G	ENSP00000487224.1:p.Met355Arg
ENST00000629785.2:c.1064T>G	ENSP00000486516.1:p.Met355Arg
ENST00000630255.2:c.1064T>G	ENSP00000486720.1:p.Met355Arg
ENST00000630370.2:c.1064T>G	ENSP00000487062.1:p.Met355Arg
ENST00000630858.2:c.1064T>G	ENSP00000486514.1:p.Met355Arg
NM_001193416.2:c.1064T>G	NP_001180345.1:p.Met355Arg
NM_001193417.2:c.1016T>G	NP_001180346.1:p.Met339Arg
NM_001356.4:c.1064T>G	NP_001347.3:p.Met355Arg
NR_126093.1:n.2009T>G
XM_011543892.1:c.1064T>G	XP_011542194.1:p.Met355Arg
NM_001363819.1:c.506T>G	NP_001350748.1:p.Met169Arg
XM_011543892.2:c.1064T>G	XP_011542194.1:p.Met355Arg
XM_017029313.1:c.506T>G	XP_016884802.1:p.Met169Arg
NM_001193416.3:c.1064T>G	NP_001180345.1:p.Met355Arg
NM_001193417.3:c.1016T>G	NP_001180346.1:p.Met339Arg
NM_001356.5:c.1064T>G MANE Select	NP_001347.3:p.Met355Arg