Canonical Allele Identifier: CA2695233414

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344242del , CM000685.2:g.41344242del	GRCh38
NC_000023.10:g.41203495del , CM000685.1:g.41203495del	GRCh37
NC_000023.9:g.41088439del	NCBI36
NG_012830.1:g.15845del
NG_012830.2:g.15845del

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1000del	ENSP00000496052.2:p.Ser334HisfsTer?
ENST00000399959.7:c.865del	ENSP00000382840.3:p.Ser289HisfsTer?
ENST00000441189.4:c.769del	ENSP00000414281.3:p.Ser257HisfsTer?
ENST00000457138.7:c.820del	ENSP00000392494.2:p.Ser274HisfsTer?
ENST00000629496.3:c.868del	ENSP00000487224.1:p.Ser290HisfsTer?
ENST00000631641.2:n.911del
ENST00000642161.1:n.3067del
ENST00000642322.1:c.310del	ENSP00000496052.1:p.Ser104HisfsTer?
ENST00000642424.1:c.310del	ENSP00000496356.1:p.Ser104HisfsTer?
ENST00000642589.1:n.4190del
ENST00000642597.1:n.1042del
ENST00000642687.1:n.901del
ENST00000642722.1:n.1701del
ENST00000642763.1:n.1759del
ENST00000642793.1:c.*317del	ENSP00000493976.1:n.*317del
ENST00000642801.1:n.517del
ENST00000643820.1:n.144del
ENST00000643963.1:c.*150del	ENSP00000495264.1:n.*150del
ENST00000644073.1:c.826del	ENSP00000493475.1:p.Ser276HisfsTer?
ENST00000644074.1:c.865del	ENSP00000496663.1:p.Ser289HisfsTer?
ENST00000644109.1:c.865del	ENSP00000494952.1:p.Ser289HisfsTer?
ENST00000644307.1:n.959del
ENST00000644513.1:c.868del	ENSP00000493819.1:p.Ser290HisfsTer?
ENST00000644677.1:c.751del	ENSP00000496524.1:p.Ser251HisfsTer?
ENST00000644876.2:c.868del MANE Select	ENSP00000494040.1:p.Ser290HisfsTer?
ENST00000644958.1:n.2529del
ENST00000645080.1:c.*2090del	ENSP00000494767.1:n.*2090del
ENST00000645120.1:n.2363del
ENST00000645338.1:n.959del
ENST00000645380.1:n.2253del
ENST00000645561.1:n.2044del
ENST00000645574.1:n.3732del
ENST00000645589.1:c.868del	ENSP00000494588.1:p.Ser290HisfsTer?
ENST00000646093.1:n.52del
ENST00000646107.1:c.751del	ENSP00000494518.1:p.Ser251HisfsTer?
ENST00000646122.1:c.868del	ENSP00000496222.1:p.Ser290HisfsTer?
ENST00000646196.1:n.1837del
ENST00000646223.1:c.*861del	ENSP00000496043.1:n.*861del
ENST00000646319.1:c.868del	ENSP00000495377.1:p.Ser290HisfsTer?
ENST00000646390.1:n.3156del
ENST00000646627.1:c.310del	ENSP00000493795.1:p.Ser104HisfsTer?
ENST00000646679.1:c.310del	ENSP00000494887.1:p.Ser104HisfsTer?
ENST00000646822.1:n.1930del
ENST00000646940.1:n.1042del
ENST00000647286.1:n.966del
ENST00000399959.6:c.868del	ENSP00000382840.2:p.Ser290HisfsTer?
ENST00000441189.3:c.340+1692del	ENSP00000414281.2:n.340+1692del
ENST00000457138.6:c.820del	ENSP00000392494.2:p.Ser274HisfsTer?
ENST00000478993.5:c.868del	ENSP00000478443.1:p.Ser290HisfsTer?
ENST00000542215.5:n.916del
ENST00000625837.2:c.868del	ENSP00000486306.1:p.Ser290HisfsTer?
ENST00000626301.2:c.868del	ENSP00000486443.1:p.Ser290HisfsTer?
ENST00000629496.2:c.868del	ENSP00000487224.1:p.Ser290HisfsTer?
ENST00000629785.2:c.868del	ENSP00000486516.1:p.Ser290HisfsTer?
ENST00000630255.2:c.868del	ENSP00000486720.1:p.Ser290HisfsTer?
ENST00000630370.2:c.868del	ENSP00000487062.1:p.Ser290HisfsTer?
ENST00000630858.2:c.868del	ENSP00000486514.1:p.Ser290HisfsTer?
NM_001193416.2:c.868del	NP_001180345.1:p.Ser290HisfsTer?
NM_001193417.2:c.820del	NP_001180346.1:p.Ser274HisfsTer?
NM_001356.4:c.868del	NP_001347.3:p.Ser290HisfsTer?
NR_126093.1:n.1813del
XM_011543892.1:c.868del	XP_011542194.1:p.Ser290HisfsTer?
NM_001363819.1:c.310del	NP_001350748.1:p.Ser104HisfsTer?
XM_011543892.2:c.868del	XP_011542194.1:p.Ser290HisfsTer?
XM_017029313.1:c.310del	XP_016884802.1:p.Ser104HisfsTer?
NM_001193416.3:c.868del	NP_001180345.1:p.Ser290HisfsTer?
NM_001193417.3:c.820del	NP_001180346.1:p.Ser274HisfsTer?
NM_001356.5:c.868del MANE Select	NP_001347.3:p.Ser290HisfsTer?