Canonical Allele Identifier: CA2425881027

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345189G= , CM000685.2:g.41345189G=	GRCh38
NC_000023.10:g.41204442G= , CM000685.1:g.41204442G=	GRCh37
NC_000023.9:g.41089386G=	NCBI36
NG_012830.1:g.16792G=
NG_012830.2:g.16792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1167G=	ENSP00000496052.2:p.Val389=
ENST00000399959.7:c.1032G=	ENSP00000382840.3:p.Val344=
ENST00000441189.4:c.936G=	ENSP00000414281.3:p.Val312=
ENST00000457138.7:c.987G=	ENSP00000392494.2:p.Val329=
ENST00000629496.3:c.1035G=	ENSP00000487224.1:p.Val345=
ENST00000642161.1:n.3234G=
ENST00000642322.1:c.477G=	ENSP00000496052.1:p.Val159=
ENST00000642424.1:c.477G=	ENSP00000496356.1:p.Val159=
ENST00000642589.1:n.4357G=
ENST00000642597.1:n.1209G=
ENST00000642687.1:n.1068G=
ENST00000642722.1:n.1868G=
ENST00000642763.1:n.1926G=
ENST00000642793.1:c.*484G=	ENSP00000493976.1:n.*484G=
ENST00000642801.1:n.684G=
ENST00000643820.1:n.311G=
ENST00000643963.1:c.*317G=	ENSP00000495264.1:n.*317G=
ENST00000644073.1:c.993G=	ENSP00000493475.1:p.Val331=
ENST00000644074.1:c.1032G=	ENSP00000496663.1:p.Val344=
ENST00000644109.1:c.1197G=	ENSP00000494952.1:p.Val399=
ENST00000644307.1:n.1126G=
ENST00000644513.1:c.1035G=	ENSP00000493819.1:p.Val345=
ENST00000644677.1:c.918G=	ENSP00000496524.1:p.Val306=
ENST00000644876.2:c.1035G= MANE Select	ENSP00000494040.1:p.Val345=
ENST00000644958.1:n.2696G=
ENST00000645080.1:c.*2257G=	ENSP00000494767.1:n.*2257G=
ENST00000645120.1:n.2530G=
ENST00000645338.1:n.1126G=
ENST00000645380.1:n.2420G=
ENST00000645561.1:n.2211G=
ENST00000645574.1:n.3899G=
ENST00000645589.1:c.1035G=	ENSP00000494588.1:p.Val345=
ENST00000646093.1:n.219G=
ENST00000646107.1:c.918G=	ENSP00000494518.1:p.Val306=
ENST00000646122.1:c.1035G=	ENSP00000496222.1:p.Val345=
ENST00000646196.1:n.2004G=
ENST00000646223.1:c.*1028G=	ENSP00000496043.1:n.*1028G=
ENST00000646319.1:c.1035G=	ENSP00000495377.1:p.Val345=
ENST00000646390.1:n.3323G=
ENST00000646627.1:c.477G=	ENSP00000493795.1:p.Val159=
ENST00000646679.1:c.477G=	ENSP00000494887.1:p.Val159=
ENST00000646822.1:n.2097G=
ENST00000646940.1:n.1209G=
ENST00000647286.1:n.1133G=
ENST00000399959.6:c.1035G=	ENSP00000382840.2:p.Val345=
ENST00000441189.3:c.341-2451G=	ENSP00000414281.2:n.341-2451G=
ENST00000457138.6:c.987G=	ENSP00000392494.2:p.Val329=
ENST00000478993.5:c.1035G=	ENSP00000478443.1:p.Val345=
ENST00000542215.5:n.1083G=
ENST00000625837.2:c.1035G=	ENSP00000486306.1:p.Val345=
ENST00000626301.2:c.1035G=	ENSP00000486443.1:p.Val345=
ENST00000629496.2:c.1035G=	ENSP00000487224.1:p.Val345=
ENST00000629785.2:c.1035G=	ENSP00000486516.1:p.Val345=
ENST00000630255.2:c.1035G=	ENSP00000486720.1:p.Val345=
ENST00000630370.2:c.1035G=	ENSP00000487062.1:p.Val345=
ENST00000630858.2:c.1035G=	ENSP00000486514.1:p.Val345=
NM_001193416.2:c.1035G=	NP_001180345.1:p.Val345=
NM_001193417.2:c.987G=	NP_001180346.1:p.Val329=
NM_001356.4:c.1035G=	NP_001347.3:p.Val345=
NR_126093.1:n.1980G=
XM_011543892.1:c.1035G=	XP_011542194.1:p.Val345=
NM_001363819.1:c.477G=	NP_001350748.1:p.Val159=
XM_011543892.2:c.1035G=	XP_011542194.1:p.Val345=
XM_017029313.1:c.477G=	XP_016884802.1:p.Val159=
NM_001193416.3:c.1035G=	NP_001180345.1:p.Val345=
NM_001193417.3:c.987G=	NP_001180346.1:p.Val329=
NM_001356.5:c.1035G= MANE Select	NP_001347.3:p.Val345=