Canonical Allele Identifier: CA2425881496
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346551A= , CM000685.2:g.41346551A= GRCh38
NC_000023.10:g.41205804A= , CM000685.1:g.41205804A= GRCh37
NC_000023.9:g.41090748A= NCBI36
NG_012830.1:g.18154A=
NG_012830.2:g.18154A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1676A= ENSP00000496052.2:p.Asn559=
ENST00000399959.7:c.1541A= ENSP00000382840.3:p.Asn514=
ENST00000441189.4:c.1445A= ENSP00000414281.3:p.Asn482=
ENST00000457138.7:c.1496A= ENSP00000392494.2:p.Asn499=
ENST00000611968.2:c.138A=
ENST00000616050.3:c.292A=
ENST00000629496.3:c.1544A= ENSP00000487224.1:p.Asn515=
ENST00000642161.1:n.3743A=
ENST00000642322.1:c.986A= ENSP00000496052.1:p.Asn329=
ENST00000642424.1:c.986A= ENSP00000496356.1:p.Asn329=
ENST00000642589.1:n.4866A=
ENST00000642597.1:n.1718A=
ENST00000642687.1:n.1577A=
ENST00000642722.1:n.2377A=
ENST00000642763.1:n.2435A=
ENST00000642793.1:c.*993A= ENSP00000493976.1:n.*993A=
ENST00000642801.1:n.1193A=
ENST00000643820.1:n.914A=
ENST00000643963.1:c.*826A= ENSP00000495264.1:n.*826A=
ENST00000644073.1:c.1502A= ENSP00000493475.1:p.Asn501=
ENST00000644074.1:c.1541A= ENSP00000496663.1:p.Asn514=
ENST00000644109.1:c.1706A= ENSP00000494952.1:p.Asn569=
ENST00000644307.1:n.1714A=
ENST00000644513.1:c.1544A= ENSP00000493819.1:p.Asn515=
ENST00000644677.1:c.1427A= ENSP00000496524.1:p.Asn476=
ENST00000644876.2:c.1544A= MANE Select ENSP00000494040.1:p.Asn515=
ENST00000644958.1:n.3205A=
ENST00000645080.1:c.*2766A= ENSP00000494767.1:n.*2766A=
ENST00000645120.1:n.3039A=
ENST00000645338.1:n.1714A=
ENST00000645380.1:n.3008A=
ENST00000645561.1:n.2720A=
ENST00000645574.1:n.4408A=
ENST00000645589.1:c.*43A= ENSP00000494588.1:n.*43A=
ENST00000646107.1:c.1427A= ENSP00000494518.1:p.Asn476=
ENST00000646122.1:c.1544A= ENSP00000496222.1:p.Asn515=
ENST00000646196.1:n.2513A=
ENST00000646223.1:c.*1537A= ENSP00000496043.1:n.*1537A=
ENST00000646319.1:c.1544A= ENSP00000495377.1:p.Asn515=
ENST00000646390.1:n.3832A=
ENST00000646627.1:c.986A= ENSP00000493795.1:p.Asn329=
ENST00000646679.1:c.986A= ENSP00000494887.1:p.Asn329=
ENST00000646822.1:n.2606A=
ENST00000646940.1:n.1718A=
ENST00000647286.1:n.1642A=
ENST00000647477.1:n.283A=
ENST00000399959.6:c.1544A= ENSP00000382840.2:p.Asn515=
ENST00000441189.3:c.341-1089A= ENSP00000414281.2:n.341-1089A=
ENST00000457138.6:c.1496A= ENSP00000392494.2:p.Asn499=
ENST00000478993.5:c.1544A= ENSP00000478443.1:p.Asn515=
ENST00000542215.5:n.1592A=
ENST00000616050.2:c.97A=
ENST00000625837.2:c.1544A= ENSP00000486306.1:p.Asn515=
ENST00000626301.2:c.1544A= ENSP00000486443.1:p.Asn515=
ENST00000629496.2:c.1544A= ENSP00000487224.1:p.Asn515=
ENST00000629785.2:c.1544A= ENSP00000486516.1:p.Asn515=
ENST00000630255.2:c.1544A= ENSP00000486720.1:p.Asn515=
ENST00000630370.2:c.1544A= ENSP00000487062.1:p.Asn515=
ENST00000630858.2:c.1544A= ENSP00000486514.1:p.Asn515=
NM_001193416.2:c.1544A= NP_001180345.1:p.Asn515=
NM_001193417.2:c.1496A= NP_001180346.1:p.Asn499=
NM_001356.4:c.1544A= NP_001347.3:p.Asn515=
NR_126093.1:n.2489A=
XM_011543892.1:c.1544A= XP_011542194.1:p.Asn515=
NM_001363819.1:c.986A= NP_001350748.1:p.Asn329=
XM_011543892.2:c.1544A= XP_011542194.1:p.Asn515=
XM_017029313.1:c.986A= XP_016884802.1:p.Asn329=
NM_001193416.3:c.1544A= NP_001180345.1:p.Asn515=
NM_001193417.3:c.1496A= NP_001180346.1:p.Asn499=
NM_001356.5:c.1544A= MANE Select NP_001347.3:p.Asn515=