Canonical Allele Identifier: CA2425881049
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345313A= , CM000685.2:g.41345313A= GRCh38
NC_000023.10:g.41204566A= , CM000685.1:g.41204566A= GRCh37
NC_000023.9:g.41089510A= NCBI36
NG_012830.1:g.16916A=
NG_012830.2:g.16916A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1291A= ENSP00000496052.2:p.Lys431=
ENST00000399959.7:c.1156A= ENSP00000382840.3:p.Lys386=
ENST00000441189.4:c.1060A= ENSP00000414281.3:p.Lys354=
ENST00000457138.7:c.1111A= ENSP00000392494.2:p.Lys371=
ENST00000629496.3:c.1159A= ENSP00000487224.1:p.Lys387=
ENST00000642161.1:n.3358A=
ENST00000642322.1:c.601A= ENSP00000496052.1:p.Lys201=
ENST00000642424.1:c.601A= ENSP00000496356.1:p.Lys201=
ENST00000642589.1:n.4481A=
ENST00000642597.1:n.1333A=
ENST00000642687.1:n.1192A=
ENST00000642722.1:n.1992A=
ENST00000642763.1:n.2050A=
ENST00000642793.1:c.*608A= ENSP00000493976.1:n.*608A=
ENST00000642801.1:n.808A=
ENST00000643820.1:n.435A=
ENST00000643963.1:c.*441A= ENSP00000495264.1:n.*441A=
ENST00000644073.1:c.1117A= ENSP00000493475.1:p.Lys373=
ENST00000644074.1:c.1156A= ENSP00000496663.1:p.Lys386=
ENST00000644109.1:c.1321A= ENSP00000494952.1:p.Lys441=
ENST00000644307.1:n.1250A=
ENST00000644513.1:c.1159A= ENSP00000493819.1:p.Lys387=
ENST00000644677.1:c.1042A= ENSP00000496524.1:p.Lys348=
ENST00000644876.2:c.1159A= MANE Select ENSP00000494040.1:p.Lys387=
ENST00000644958.1:n.2820A=
ENST00000645080.1:c.*2381A= ENSP00000494767.1:n.*2381A=
ENST00000645120.1:n.2654A=
ENST00000645338.1:n.1250A=
ENST00000645380.1:n.2544A=
ENST00000645561.1:n.2335A=
ENST00000645574.1:n.4023A=
ENST00000645589.1:c.1159A= ENSP00000494588.1:p.Lys387=
ENST00000646093.1:n.343A=
ENST00000646107.1:c.1042A= ENSP00000494518.1:p.Lys348=
ENST00000646122.1:c.1159A= ENSP00000496222.1:p.Lys387=
ENST00000646196.1:n.2128A=
ENST00000646223.1:c.*1152A= ENSP00000496043.1:n.*1152A=
ENST00000646319.1:c.1159A= ENSP00000495377.1:p.Lys387=
ENST00000646390.1:n.3447A=
ENST00000646627.1:c.601A= ENSP00000493795.1:p.Lys201=
ENST00000646679.1:c.601A= ENSP00000494887.1:p.Lys201=
ENST00000646822.1:n.2221A=
ENST00000646940.1:n.1333A=
ENST00000647286.1:n.1257A=
ENST00000399959.6:c.1159A= ENSP00000382840.2:p.Lys387=
ENST00000441189.3:c.341-2327A= ENSP00000414281.2:n.341-2327A=
ENST00000457138.6:c.1111A= ENSP00000392494.2:p.Lys371=
ENST00000478993.5:c.1159A= ENSP00000478443.1:p.Lys387=
ENST00000542215.5:n.1207A=
ENST00000625837.2:c.1159A= ENSP00000486306.1:p.Lys387=
ENST00000626301.2:c.1159A= ENSP00000486443.1:p.Lys387=
ENST00000629496.2:c.1159A= ENSP00000487224.1:p.Lys387=
ENST00000629785.2:c.1159A= ENSP00000486516.1:p.Lys387=
ENST00000630255.2:c.1159A= ENSP00000486720.1:p.Lys387=
ENST00000630370.2:c.1159A= ENSP00000487062.1:p.Lys387=
ENST00000630858.2:c.1159A= ENSP00000486514.1:p.Lys387=
NM_001193416.2:c.1159A= NP_001180345.1:p.Lys387=
NM_001193417.2:c.1111A= NP_001180346.1:p.Lys371=
NM_001356.4:c.1159A= NP_001347.3:p.Lys387=
NR_126093.1:n.2104A=
XM_011543892.1:c.1159A= XP_011542194.1:p.Lys387=
NM_001363819.1:c.601A= NP_001350748.1:p.Lys201=
XM_011543892.2:c.1159A= XP_011542194.1:p.Lys387=
XM_017029313.1:c.601A= XP_016884802.1:p.Lys201=
NM_001193416.3:c.1159A= NP_001180345.1:p.Lys387=
NM_001193417.3:c.1111A= NP_001180346.1:p.Lys371=
NM_001356.5:c.1159A= MANE Select NP_001347.3:p.Lys387=