Canonical Allele Identifier: CA516347307

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41203506T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344253T>G , CM000685.2:g.41344253T>G	GRCh38
NC_000023.10:g.41203506T>G , CM000685.1:g.41203506T>G	GRCh37
NC_000023.9:g.41088450T>G	NCBI36
NG_012830.1:g.15856T>G
NG_012830.2:g.15856T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1011T>G	ENSP00000496052.2:p.Ser337=
ENST00000399959.7:c.876T>G	ENSP00000382840.3:p.Ser292=
ENST00000441189.4:c.780T>G	ENSP00000414281.3:p.Ser260=
ENST00000457138.7:c.831T>G	ENSP00000392494.2:p.Ser277=
ENST00000629496.3:c.879T>G	ENSP00000487224.1:p.Ser293=
ENST00000631641.2:n.922T>G
ENST00000642161.1:n.3078T>G
ENST00000642322.1:c.321T>G	ENSP00000496052.1:p.Ser107=
ENST00000642424.1:c.321T>G	ENSP00000496356.1:p.Ser107=
ENST00000642589.1:n.4201T>G
ENST00000642597.1:n.1053T>G
ENST00000642687.1:n.912T>G
ENST00000642722.1:n.1712T>G
ENST00000642763.1:n.1770T>G
ENST00000642793.1:c.*328T>G	ENSP00000493976.1:n.*328T>G
ENST00000642801.1:n.528T>G
ENST00000643820.1:n.155T>G
ENST00000643963.1:c.*161T>G	ENSP00000495264.1:n.*161T>G
ENST00000644073.1:c.837T>G	ENSP00000493475.1:p.Ser279=
ENST00000644074.1:c.876T>G	ENSP00000496663.1:p.Ser292=
ENST00000644109.1:c.876T>G	ENSP00000494952.1:p.Ser292=
ENST00000644307.1:n.970T>G
ENST00000644513.1:c.879T>G	ENSP00000493819.1:p.Ser293=
ENST00000644677.1:c.762T>G	ENSP00000496524.1:p.Ser254=
ENST00000644876.2:c.879T>G MANE Select	ENSP00000494040.1:p.Ser293=
ENST00000644958.1:n.2540T>G
ENST00000645080.1:c.*2101T>G	ENSP00000494767.1:n.*2101T>G
ENST00000645120.1:n.2374T>G
ENST00000645338.1:n.970T>G
ENST00000645380.1:n.2264T>G
ENST00000645561.1:n.2055T>G
ENST00000645574.1:n.3743T>G
ENST00000645589.1:c.879T>G	ENSP00000494588.1:p.Ser293=
ENST00000646093.1:n.63T>G
ENST00000646107.1:c.762T>G	ENSP00000494518.1:p.Ser254=
ENST00000646122.1:c.879T>G	ENSP00000496222.1:p.Ser293=
ENST00000646196.1:n.1848T>G
ENST00000646223.1:c.*872T>G	ENSP00000496043.1:n.*872T>G
ENST00000646319.1:c.879T>G	ENSP00000495377.1:p.Ser293=
ENST00000646390.1:n.3167T>G
ENST00000646627.1:c.321T>G	ENSP00000493795.1:p.Ser107=
ENST00000646679.1:c.321T>G	ENSP00000494887.1:p.Ser107=
ENST00000646822.1:n.1941T>G
ENST00000646940.1:n.1053T>G
ENST00000647286.1:n.977T>G
ENST00000399959.6:c.879T>G	ENSP00000382840.2:p.Ser293=
ENST00000441189.3:c.340+1703T>G	ENSP00000414281.2:n.340+1703T>G
ENST00000457138.6:c.831T>G	ENSP00000392494.2:p.Ser277=
ENST00000478993.5:c.879T>G	ENSP00000478443.1:p.Ser293=
ENST00000542215.5:n.927T>G
ENST00000625837.2:c.879T>G	ENSP00000486306.1:p.Ser293=
ENST00000626301.2:c.879T>G	ENSP00000486443.1:p.Ser293=
ENST00000629496.2:c.879T>G	ENSP00000487224.1:p.Ser293=
ENST00000629785.2:c.879T>G	ENSP00000486516.1:p.Ser293=
ENST00000630255.2:c.879T>G	ENSP00000486720.1:p.Ser293=
ENST00000630370.2:c.879T>G	ENSP00000487062.1:p.Ser293=
ENST00000630858.2:c.879T>G	ENSP00000486514.1:p.Ser293=
NM_001193416.2:c.879T>G	NP_001180345.1:p.Ser293=
NM_001193417.2:c.831T>G	NP_001180346.1:p.Ser277=
NM_001356.4:c.879T>G	NP_001347.3:p.Ser293=
NR_126093.1:n.1824T>G
XM_011543892.1:c.879T>G	XP_011542194.1:p.Ser293=
NM_001363819.1:c.321T>G	NP_001350748.1:p.Ser107=
XM_011543892.2:c.879T>G	XP_011542194.1:p.Ser293=
XM_017029313.1:c.321T>G	XP_016884802.1:p.Ser107=
NM_001193416.3:c.879T>G	NP_001180345.1:p.Ser293=
NM_001193417.3:c.831T>G	NP_001180346.1:p.Ser277=
NM_001356.5:c.879T>G MANE Select	NP_001347.3:p.Ser293=