Canonical Allele Identifier: CA2425881098
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41345524C= , CM000685.2:g.41345524C= GRCh38
NC_000023.10:g.41204777C= , CM000685.1:g.41204777C= GRCh37
NC_000023.9:g.41089721C= NCBI36
NG_012830.1:g.17127C=
NG_012830.2:g.17127C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1423C= ENSP00000496052.2:p.Leu475=
ENST00000399959.7:c.1288C= ENSP00000382840.3:p.Leu430=
ENST00000441189.4:c.1192C= ENSP00000414281.3:p.Leu398=
ENST00000457138.7:c.1243C= ENSP00000392494.2:p.Leu415=
ENST00000616050.3:c.39C=
ENST00000629496.3:c.1291C= ENSP00000487224.1:p.Leu431=
ENST00000642161.1:n.3490C=
ENST00000642322.1:c.733C= ENSP00000496052.1:p.Leu245=
ENST00000642424.1:c.733C= ENSP00000496356.1:p.Leu245=
ENST00000642589.1:n.4613C=
ENST00000642597.1:n.1465C=
ENST00000642687.1:n.1324C=
ENST00000642722.1:n.2124C=
ENST00000642763.1:n.2182C=
ENST00000642793.1:c.*740C= ENSP00000493976.1:n.*740C=
ENST00000642801.1:n.940C=
ENST00000643820.1:n.567C=
ENST00000643963.1:c.*573C= ENSP00000495264.1:n.*573C=
ENST00000644073.1:c.1249C= ENSP00000493475.1:p.Leu417=
ENST00000644074.1:c.1288C= ENSP00000496663.1:p.Leu430=
ENST00000644109.1:c.1453C= ENSP00000494952.1:p.Leu485=
ENST00000644307.1:n.1461C=
ENST00000644513.1:c.1291C= ENSP00000493819.1:p.Leu431=
ENST00000644677.1:c.1174C= ENSP00000496524.1:p.Leu392=
ENST00000644876.2:c.1291C= MANE Select ENSP00000494040.1:p.Leu431=
ENST00000644958.1:n.2952C=
ENST00000645080.1:c.*2513C= ENSP00000494767.1:n.*2513C=
ENST00000645120.1:n.2786C=
ENST00000645338.1:n.1461C=
ENST00000645380.1:n.2755C=
ENST00000645561.1:n.2467C=
ENST00000645574.1:n.4155C=
ENST00000645589.1:c.1291C= ENSP00000494588.1:p.Leu431=
ENST00000646093.1:n.475C=
ENST00000646107.1:c.1174C= ENSP00000494518.1:p.Leu392=
ENST00000646122.1:c.1291C= ENSP00000496222.1:p.Leu431=
ENST00000646196.1:n.2260C=
ENST00000646223.1:c.*1284C= ENSP00000496043.1:n.*1284C=
ENST00000646319.1:c.1291C= ENSP00000495377.1:p.Leu431=
ENST00000646390.1:n.3579C=
ENST00000646627.1:c.733C= ENSP00000493795.1:p.Leu245=
ENST00000646679.1:c.733C= ENSP00000494887.1:p.Leu245=
ENST00000646822.1:n.2353C=
ENST00000646940.1:n.1465C=
ENST00000647286.1:n.1389C=
ENST00000647477.1:n.30C=
ENST00000399959.6:c.1291C= ENSP00000382840.2:p.Leu431=
ENST00000441189.3:c.341-2116C= ENSP00000414281.2:n.341-2116C=
ENST00000457138.6:c.1243C= ENSP00000392494.2:p.Leu415=
ENST00000478993.5:c.1291C= ENSP00000478443.1:p.Leu431=
ENST00000542215.5:n.1339C=
ENST00000625837.2:c.1291C= ENSP00000486306.1:p.Leu431=
ENST00000626301.2:c.1291C= ENSP00000486443.1:p.Leu431=
ENST00000629496.2:c.1291C= ENSP00000487224.1:p.Leu431=
ENST00000629785.2:c.1291C= ENSP00000486516.1:p.Leu431=
ENST00000630255.2:c.1291C= ENSP00000486720.1:p.Leu431=
ENST00000630370.2:c.1291C= ENSP00000487062.1:p.Leu431=
ENST00000630858.2:c.1291C= ENSP00000486514.1:p.Leu431=
NM_001193416.2:c.1291C= NP_001180345.1:p.Leu431=
NM_001193417.2:c.1243C= NP_001180346.1:p.Leu415=
NM_001356.4:c.1291C= NP_001347.3:p.Leu431=
NR_126093.1:n.2236C=
XM_011543892.1:c.1291C= XP_011542194.1:p.Leu431=
NM_001363819.1:c.733C= NP_001350748.1:p.Leu245=
XM_011543892.2:c.1291C= XP_011542194.1:p.Leu431=
XM_017029313.1:c.733C= XP_016884802.1:p.Leu245=
NM_001193416.3:c.1291C= NP_001180345.1:p.Leu431=
NM_001193417.3:c.1243C= NP_001180346.1:p.Leu415=
NM_001356.5:c.1291C= MANE Select NP_001347.3:p.Leu431=