Canonical Allele Identifier: CA412771466

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204539A>T (hg19) ; chrX:g.41345286A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345286A>T , CM000685.2:g.41345286A>T	GRCh38
NC_000023.10:g.41204539A>T , CM000685.1:g.41204539A>T	GRCh37
NC_000023.9:g.41089483A>T	NCBI36
NG_012830.1:g.16889A>T
NG_012830.2:g.16889A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1264A>T	ENSP00000496052.2:p.Thr422Ser
ENST00000399959.7:c.1129A>T	ENSP00000382840.3:p.Thr377Ser
ENST00000441189.4:c.1033A>T	ENSP00000414281.3:p.Thr345Ser
ENST00000457138.7:c.1084A>T	ENSP00000392494.2:p.Thr362Ser
ENST00000629496.3:c.1132A>T	ENSP00000487224.1:p.Thr378Ser
ENST00000642161.1:n.3331A>T
ENST00000642322.1:c.574A>T	ENSP00000496052.1:p.Thr192Ser
ENST00000642424.1:c.574A>T	ENSP00000496356.1:p.Thr192Ser
ENST00000642589.1:n.4454A>T
ENST00000642597.1:n.1306A>T
ENST00000642687.1:n.1165A>T
ENST00000642722.1:n.1965A>T
ENST00000642763.1:n.2023A>T
ENST00000642793.1:c.*581A>T	ENSP00000493976.1:n.*581A>T
ENST00000642801.1:n.781A>T
ENST00000643820.1:n.408A>T
ENST00000643963.1:c.*414A>T	ENSP00000495264.1:n.*414A>T
ENST00000644073.1:c.1090A>T	ENSP00000493475.1:p.Thr364Ser
ENST00000644074.1:c.1129A>T	ENSP00000496663.1:p.Thr377Ser
ENST00000644109.1:c.1294A>T	ENSP00000494952.1:p.Thr432Ser
ENST00000644307.1:n.1223A>T
ENST00000644513.1:c.1132A>T	ENSP00000493819.1:p.Thr378Ser
ENST00000644677.1:c.1015A>T	ENSP00000496524.1:p.Thr339Ser
ENST00000644876.2:c.1132A>T MANE Select	ENSP00000494040.1:p.Thr378Ser
ENST00000644958.1:n.2793A>T
ENST00000645080.1:c.*2354A>T	ENSP00000494767.1:n.*2354A>T
ENST00000645120.1:n.2627A>T
ENST00000645338.1:n.1223A>T
ENST00000645380.1:n.2517A>T
ENST00000645561.1:n.2308A>T
ENST00000645574.1:n.3996A>T
ENST00000645589.1:c.1132A>T	ENSP00000494588.1:p.Thr378Ser
ENST00000646093.1:n.316A>T
ENST00000646107.1:c.1015A>T	ENSP00000494518.1:p.Thr339Ser
ENST00000646122.1:c.1132A>T	ENSP00000496222.1:p.Thr378Ser
ENST00000646196.1:n.2101A>T
ENST00000646223.1:c.*1125A>T	ENSP00000496043.1:n.*1125A>T
ENST00000646319.1:c.1132A>T	ENSP00000495377.1:p.Thr378Ser
ENST00000646390.1:n.3420A>T
ENST00000646627.1:c.574A>T	ENSP00000493795.1:p.Thr192Ser
ENST00000646679.1:c.574A>T	ENSP00000494887.1:p.Thr192Ser
ENST00000646822.1:n.2194A>T
ENST00000646940.1:n.1306A>T
ENST00000647286.1:n.1230A>T
ENST00000399959.6:c.1132A>T	ENSP00000382840.2:p.Thr378Ser
ENST00000441189.3:c.341-2354A>T	ENSP00000414281.2:n.341-2354A>T
ENST00000457138.6:c.1084A>T	ENSP00000392494.2:p.Thr362Ser
ENST00000478993.5:c.1132A>T	ENSP00000478443.1:p.Thr378Ser
ENST00000542215.5:n.1180A>T
ENST00000625837.2:c.1132A>T	ENSP00000486306.1:p.Thr378Ser
ENST00000626301.2:c.1132A>T	ENSP00000486443.1:p.Thr378Ser
ENST00000629496.2:c.1132A>T	ENSP00000487224.1:p.Thr378Ser
ENST00000629785.2:c.1132A>T	ENSP00000486516.1:p.Thr378Ser
ENST00000630255.2:c.1132A>T	ENSP00000486720.1:p.Thr378Ser
ENST00000630370.2:c.1132A>T	ENSP00000487062.1:p.Thr378Ser
ENST00000630858.2:c.1132A>T	ENSP00000486514.1:p.Thr378Ser
NM_001193416.2:c.1132A>T	NP_001180345.1:p.Thr378Ser
NM_001193417.2:c.1084A>T	NP_001180346.1:p.Thr362Ser
NM_001356.4:c.1132A>T	NP_001347.3:p.Thr378Ser
NR_126093.1:n.2077A>T
XM_011543892.1:c.1132A>T	XP_011542194.1:p.Thr378Ser
NM_001363819.1:c.574A>T	NP_001350748.1:p.Thr192Ser
XM_011543892.2:c.1132A>T	XP_011542194.1:p.Thr378Ser
XM_017029313.1:c.574A>T	XP_016884802.1:p.Thr192Ser
NM_001193416.3:c.1132A>T	NP_001180345.1:p.Thr378Ser
NM_001193417.3:c.1084A>T	NP_001180346.1:p.Thr362Ser
NM_001356.5:c.1132A>T MANE Select	NP_001347.3:p.Thr378Ser