Canonical Allele Identifier: CA515972361

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205492A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346239A>T , CM000685.2:g.41346239A>T	GRCh38
NC_000023.10:g.41205492A>T , CM000685.1:g.41205492A>T	GRCh37
NC_000023.9:g.41090436A>T	NCBI36
NG_012830.1:g.17842A>T
NG_012830.2:g.17842A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1458A>T	ENSP00000496052.2:p.Ser486=
ENST00000399959.7:c.1323A>T	ENSP00000382840.3:p.Ser441=
ENST00000441189.4:c.1227A>T	ENSP00000414281.3:p.Ser409=
ENST00000457138.7:c.1278A>T	ENSP00000392494.2:p.Ser426=
ENST00000616050.3:c.74A>T
ENST00000629496.3:c.1326A>T	ENSP00000487224.1:p.Ser442=
ENST00000642161.1:n.3525A>T
ENST00000642322.1:c.768A>T	ENSP00000496052.1:p.Ser256=
ENST00000642424.1:c.768A>T	ENSP00000496356.1:p.Ser256=
ENST00000642589.1:n.4648A>T
ENST00000642597.1:n.1500A>T
ENST00000642687.1:n.1359A>T
ENST00000642722.1:n.2159A>T
ENST00000642763.1:n.2217A>T
ENST00000642793.1:c.*775A>T	ENSP00000493976.1:n.*775A>T
ENST00000642801.1:n.975A>T
ENST00000643820.1:n.602A>T
ENST00000643963.1:c.*608A>T	ENSP00000495264.1:n.*608A>T
ENST00000644073.1:c.1284A>T	ENSP00000493475.1:p.Ser428=
ENST00000644074.1:c.1323A>T	ENSP00000496663.1:p.Ser441=
ENST00000644109.1:c.1488A>T	ENSP00000494952.1:p.Ser496=
ENST00000644307.1:n.1496A>T
ENST00000644513.1:c.1326A>T	ENSP00000493819.1:p.Ser442=
ENST00000644677.1:c.1209A>T	ENSP00000496524.1:p.Ser403=
ENST00000644876.2:c.1326A>T MANE Select	ENSP00000494040.1:p.Ser442=
ENST00000644958.1:n.2987A>T
ENST00000645080.1:c.*2548A>T	ENSP00000494767.1:n.*2548A>T
ENST00000645120.1:n.2821A>T
ENST00000645338.1:n.1496A>T
ENST00000645380.1:n.2790A>T
ENST00000645561.1:n.2502A>T
ENST00000645574.1:n.4190A>T
ENST00000645589.1:c.1326A>T	ENSP00000494588.1:p.Ser442=
ENST00000646093.1:n.510A>T
ENST00000646107.1:c.1209A>T	ENSP00000494518.1:p.Ser403=
ENST00000646122.1:c.1326A>T	ENSP00000496222.1:p.Ser442=
ENST00000646196.1:n.2295A>T
ENST00000646223.1:c.*1319A>T	ENSP00000496043.1:n.*1319A>T
ENST00000646319.1:c.1326A>T	ENSP00000495377.1:p.Ser442=
ENST00000646390.1:n.3614A>T
ENST00000646627.1:c.768A>T	ENSP00000493795.1:p.Ser256=
ENST00000646679.1:c.768A>T	ENSP00000494887.1:p.Ser256=
ENST00000646822.1:n.2388A>T
ENST00000646940.1:n.1500A>T
ENST00000647286.1:n.1424A>T
ENST00000647477.1:n.65A>T
ENST00000399959.6:c.1326A>T	ENSP00000382840.2:p.Ser442=
ENST00000441189.3:c.341-1401A>T	ENSP00000414281.2:n.341-1401A>T
ENST00000457138.6:c.1278A>T	ENSP00000392494.2:p.Ser426=
ENST00000478993.5:c.1326A>T	ENSP00000478443.1:p.Ser442=
ENST00000542215.5:n.1374A>T
ENST00000625837.2:c.1326A>T	ENSP00000486306.1:p.Ser442=
ENST00000626301.2:c.1326A>T	ENSP00000486443.1:p.Ser442=
ENST00000629496.2:c.1326A>T	ENSP00000487224.1:p.Ser442=
ENST00000629785.2:c.1326A>T	ENSP00000486516.1:p.Ser442=
ENST00000630255.2:c.1326A>T	ENSP00000486720.1:p.Ser442=
ENST00000630370.2:c.1326A>T	ENSP00000487062.1:p.Ser442=
ENST00000630858.2:c.1326A>T	ENSP00000486514.1:p.Ser442=
NM_001193416.2:c.1326A>T	NP_001180345.1:p.Ser442=
NM_001193417.2:c.1278A>T	NP_001180346.1:p.Ser426=
NM_001356.4:c.1326A>T	NP_001347.3:p.Ser442=
NR_126093.1:n.2271A>T
XM_011543892.1:c.1326A>T	XP_011542194.1:p.Ser442=
NM_001363819.1:c.768A>T	NP_001350748.1:p.Ser256=
XM_011543892.2:c.1326A>T	XP_011542194.1:p.Ser442=
XM_017029313.1:c.768A>T	XP_016884802.1:p.Ser256=
NM_001193416.3:c.1326A>T	NP_001180345.1:p.Ser442=
NM_001193417.3:c.1278A>T	NP_001180346.1:p.Ser426=
NM_001356.5:c.1326A>T MANE Select	NP_001347.3:p.Ser442=