Canonical Allele Identifier: CA2425881498
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346571A= , CM000685.2:g.41346571A= GRCh38
NC_000023.10:g.41205824A= , CM000685.1:g.41205824A= GRCh37
NC_000023.9:g.41090768A= NCBI36
NG_012830.1:g.18174A=
NG_012830.2:g.18174A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1696A= ENSP00000496052.2:p.Ile566=
ENST00000399959.7:c.1561A= ENSP00000382840.3:p.Ile521=
ENST00000441189.4:c.1465A= ENSP00000414281.3:p.Ile489=
ENST00000457138.7:c.1516A= ENSP00000392494.2:p.Ile506=
ENST00000611968.2:c.158A=
ENST00000616050.3:c.312A=
ENST00000629496.3:c.1564A= ENSP00000487224.1:p.Ile522=
ENST00000642161.1:n.3763A=
ENST00000642322.1:c.1006A= ENSP00000496052.1:p.Ile336=
ENST00000642424.1:c.1006A= ENSP00000496356.1:p.Ile336=
ENST00000642589.1:n.4886A=
ENST00000642597.1:n.1738A=
ENST00000642687.1:n.1597A=
ENST00000642722.1:n.2397A=
ENST00000642763.1:n.2455A=
ENST00000642793.1:c.*1013A= ENSP00000493976.1:n.*1013A=
ENST00000642801.1:n.1213A=
ENST00000643820.1:n.934A=
ENST00000643963.1:c.*846A= ENSP00000495264.1:n.*846A=
ENST00000644073.1:c.1522A= ENSP00000493475.1:p.Ile508=
ENST00000644074.1:c.1561A= ENSP00000496663.1:p.Ile521=
ENST00000644109.1:c.1726A= ENSP00000494952.1:p.Ile576=
ENST00000644307.1:n.1734A=
ENST00000644513.1:c.1564A= ENSP00000493819.1:p.Ile522=
ENST00000644677.1:c.1447A= ENSP00000496524.1:p.Ile483=
ENST00000644876.2:c.1564A= MANE Select ENSP00000494040.1:p.Ile522=
ENST00000644958.1:n.3225A=
ENST00000645080.1:c.*2786A= ENSP00000494767.1:n.*2786A=
ENST00000645120.1:n.3059A=
ENST00000645338.1:n.1734A=
ENST00000645380.1:n.3028A=
ENST00000645561.1:n.2740A=
ENST00000645574.1:n.4428A=
ENST00000645589.1:c.*63A= ENSP00000494588.1:n.*63A=
ENST00000646107.1:c.1447A= ENSP00000494518.1:p.Ile483=
ENST00000646122.1:c.1564A= ENSP00000496222.1:p.Ile522=
ENST00000646196.1:n.2533A=
ENST00000646223.1:c.*1557A= ENSP00000496043.1:n.*1557A=
ENST00000646319.1:c.1564A= ENSP00000495377.1:p.Ile522=
ENST00000646390.1:n.3852A=
ENST00000646627.1:c.1006A= ENSP00000493795.1:p.Ile336=
ENST00000646679.1:c.1006A= ENSP00000494887.1:p.Ile336=
ENST00000646822.1:n.2626A=
ENST00000646940.1:n.1738A=
ENST00000647286.1:n.1662A=
ENST00000647477.1:n.303A=
ENST00000399959.6:c.1564A= ENSP00000382840.2:p.Ile522=
ENST00000441189.3:c.341-1069A= ENSP00000414281.2:n.341-1069A=
ENST00000457138.6:c.1516A= ENSP00000392494.2:p.Ile506=
ENST00000478993.5:c.1564A= ENSP00000478443.1:p.Ile522=
ENST00000611968.1:c.6A=
ENST00000616050.2:c.117A=
ENST00000625837.2:c.1564A= ENSP00000486306.1:p.Ile522=
ENST00000626301.2:c.1564A= ENSP00000486443.1:p.Ile522=
ENST00000629496.2:c.1564A= ENSP00000487224.1:p.Ile522=
ENST00000629785.2:c.1564A= ENSP00000486516.1:p.Ile522=
ENST00000630255.2:c.1564A= ENSP00000486720.1:p.Ile522=
ENST00000630370.2:c.1564A= ENSP00000487062.1:p.Ile522=
ENST00000630858.2:c.1564A= ENSP00000486514.1:p.Ile522=
NM_001193416.2:c.1564A= NP_001180345.1:p.Ile522=
NM_001193417.2:c.1516A= NP_001180346.1:p.Ile506=
NM_001356.4:c.1564A= NP_001347.3:p.Ile522=
NR_126093.1:n.2509A=
XM_011543892.1:c.1564A= XP_011542194.1:p.Ile522=
NM_001363819.1:c.1006A= NP_001350748.1:p.Ile336=
XM_011543892.2:c.1564A= XP_011542194.1:p.Ile522=
XM_017029313.1:c.1006A= XP_016884802.1:p.Ile336=
NM_001193416.3:c.1564A= NP_001180345.1:p.Ile522=
NM_001193417.3:c.1516A= NP_001180346.1:p.Ile506=
NM_001356.5:c.1564A= MANE Select NP_001347.3:p.Ile522=