Canonical Allele Identifier: CA515972373

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205504G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346251G>T , CM000685.2:g.41346251G>T	GRCh38
NC_000023.10:g.41205504G>T , CM000685.1:g.41205504G>T	GRCh37
NC_000023.9:g.41090448G>T	NCBI36
NG_012830.1:g.17854G>T
NG_012830.2:g.17854G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1470G>T	ENSP00000496052.2:p.Val490=
ENST00000399959.7:c.1335G>T	ENSP00000382840.3:p.Val445=
ENST00000441189.4:c.1239G>T	ENSP00000414281.3:p.Val413=
ENST00000457138.7:c.1290G>T	ENSP00000392494.2:p.Val430=
ENST00000616050.3:c.86G>T
ENST00000629496.3:c.1338G>T	ENSP00000487224.1:p.Val446=
ENST00000642161.1:n.3537G>T
ENST00000642322.1:c.780G>T	ENSP00000496052.1:p.Val260=
ENST00000642424.1:c.780G>T	ENSP00000496356.1:p.Val260=
ENST00000642589.1:n.4660G>T
ENST00000642597.1:n.1512G>T
ENST00000642687.1:n.1371G>T
ENST00000642722.1:n.2171G>T
ENST00000642763.1:n.2229G>T
ENST00000642793.1:c.*787G>T	ENSP00000493976.1:n.*787G>T
ENST00000642801.1:n.987G>T
ENST00000643820.1:n.614G>T
ENST00000643963.1:c.*620G>T	ENSP00000495264.1:n.*620G>T
ENST00000644073.1:c.1296G>T	ENSP00000493475.1:p.Val432=
ENST00000644074.1:c.1335G>T	ENSP00000496663.1:p.Val445=
ENST00000644109.1:c.1500G>T	ENSP00000494952.1:p.Val500=
ENST00000644307.1:n.1508G>T
ENST00000644513.1:c.1338G>T	ENSP00000493819.1:p.Val446=
ENST00000644677.1:c.1221G>T	ENSP00000496524.1:p.Val407=
ENST00000644876.2:c.1338G>T MANE Select	ENSP00000494040.1:p.Val446=
ENST00000644958.1:n.2999G>T
ENST00000645080.1:c.*2560G>T	ENSP00000494767.1:n.*2560G>T
ENST00000645120.1:n.2833G>T
ENST00000645338.1:n.1508G>T
ENST00000645380.1:n.2802G>T
ENST00000645561.1:n.2514G>T
ENST00000645574.1:n.4202G>T
ENST00000645589.1:c.1338G>T	ENSP00000494588.1:p.Val446=
ENST00000646093.1:n.522G>T
ENST00000646107.1:c.1221G>T	ENSP00000494518.1:p.Val407=
ENST00000646122.1:c.1338G>T	ENSP00000496222.1:p.Val446=
ENST00000646196.1:n.2307G>T
ENST00000646223.1:c.*1331G>T	ENSP00000496043.1:n.*1331G>T
ENST00000646319.1:c.1338G>T	ENSP00000495377.1:p.Val446=
ENST00000646390.1:n.3626G>T
ENST00000646627.1:c.780G>T	ENSP00000493795.1:p.Val260=
ENST00000646679.1:c.780G>T	ENSP00000494887.1:p.Val260=
ENST00000646822.1:n.2400G>T
ENST00000646940.1:n.1512G>T
ENST00000647286.1:n.1436G>T
ENST00000647477.1:n.77G>T
ENST00000399959.6:c.1338G>T	ENSP00000382840.2:p.Val446=
ENST00000441189.3:c.341-1389G>T	ENSP00000414281.2:n.341-1389G>T
ENST00000457138.6:c.1290G>T	ENSP00000392494.2:p.Val430=
ENST00000478993.5:c.1338G>T	ENSP00000478443.1:p.Val446=
ENST00000542215.5:n.1386G>T
ENST00000625837.2:c.1338G>T	ENSP00000486306.1:p.Val446=
ENST00000626301.2:c.1338G>T	ENSP00000486443.1:p.Val446=
ENST00000629496.2:c.1338G>T	ENSP00000487224.1:p.Val446=
ENST00000629785.2:c.1338G>T	ENSP00000486516.1:p.Val446=
ENST00000630255.2:c.1338G>T	ENSP00000486720.1:p.Val446=
ENST00000630370.2:c.1338G>T	ENSP00000487062.1:p.Val446=
ENST00000630858.2:c.1338G>T	ENSP00000486514.1:p.Val446=
NM_001193416.2:c.1338G>T	NP_001180345.1:p.Val446=
NM_001193417.2:c.1290G>T	NP_001180346.1:p.Val430=
NM_001356.4:c.1338G>T	NP_001347.3:p.Val446=
NR_126093.1:n.2283G>T
XM_011543892.1:c.1338G>T	XP_011542194.1:p.Val446=
NM_001363819.1:c.780G>T	NP_001350748.1:p.Val260=
XM_011543892.2:c.1338G>T	XP_011542194.1:p.Val446=
XM_017029313.1:c.780G>T	XP_016884802.1:p.Val260=
NM_001193416.3:c.1338G>T	NP_001180345.1:p.Val446=
NM_001193417.3:c.1290G>T	NP_001180346.1:p.Val430=
NM_001356.5:c.1338G>T MANE Select	NP_001347.3:p.Val446=