Canonical Allele Identifier: CA412776654

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205822A>T (hg19) ; chrX:g.41346569A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346569A>T , CM000685.2:g.41346569A>T	GRCh38
NC_000023.10:g.41205822A>T , CM000685.1:g.41205822A>T	GRCh37
NC_000023.9:g.41090766A>T	NCBI36
NG_012830.1:g.18172A>T
NG_012830.2:g.18172A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1694A>T	ENSP00000496052.2:p.Asp565Val
ENST00000399959.7:c.1559A>T	ENSP00000382840.3:p.Asp520Val
ENST00000441189.4:c.1463A>T	ENSP00000414281.3:p.Asp488Val
ENST00000457138.7:c.1514A>T	ENSP00000392494.2:p.Asp505Val
ENST00000611968.2:c.156A>T
ENST00000616050.3:c.310A>T
ENST00000629496.3:c.1562A>T	ENSP00000487224.1:p.Asp521Val
ENST00000642161.1:n.3761A>T
ENST00000642322.1:c.1004A>T	ENSP00000496052.1:p.Asp335Val
ENST00000642424.1:c.1004A>T	ENSP00000496356.1:p.Asp335Val
ENST00000642589.1:n.4884A>T
ENST00000642597.1:n.1736A>T
ENST00000642687.1:n.1595A>T
ENST00000642722.1:n.2395A>T
ENST00000642763.1:n.2453A>T
ENST00000642793.1:c.*1011A>T	ENSP00000493976.1:n.*1011A>T
ENST00000642801.1:n.1211A>T
ENST00000643820.1:n.932A>T
ENST00000643963.1:c.*844A>T	ENSP00000495264.1:n.*844A>T
ENST00000644073.1:c.1520A>T	ENSP00000493475.1:p.Asp507Val
ENST00000644074.1:c.1559A>T	ENSP00000496663.1:p.Asp520Val
ENST00000644109.1:c.1724A>T	ENSP00000494952.1:p.Asp575Val
ENST00000644307.1:n.1732A>T
ENST00000644513.1:c.1562A>T	ENSP00000493819.1:p.Asp521Val
ENST00000644677.1:c.1445A>T	ENSP00000496524.1:p.Asp482Val
ENST00000644876.2:c.1562A>T MANE Select	ENSP00000494040.1:p.Asp521Val
ENST00000644958.1:n.3223A>T
ENST00000645080.1:c.*2784A>T	ENSP00000494767.1:n.*2784A>T
ENST00000645120.1:n.3057A>T
ENST00000645338.1:n.1732A>T
ENST00000645380.1:n.3026A>T
ENST00000645561.1:n.2738A>T
ENST00000645574.1:n.4426A>T
ENST00000645589.1:c.*61A>T	ENSP00000494588.1:n.*61A>T
ENST00000646107.1:c.1445A>T	ENSP00000494518.1:p.Asp482Val
ENST00000646122.1:c.1562A>T	ENSP00000496222.1:p.Asp521Val
ENST00000646196.1:n.2531A>T
ENST00000646223.1:c.*1555A>T	ENSP00000496043.1:n.*1555A>T
ENST00000646319.1:c.1562A>T	ENSP00000495377.1:p.Asp521Val
ENST00000646390.1:n.3850A>T
ENST00000646627.1:c.1004A>T	ENSP00000493795.1:p.Asp335Val
ENST00000646679.1:c.1004A>T	ENSP00000494887.1:p.Asp335Val
ENST00000646822.1:n.2624A>T
ENST00000646940.1:n.1736A>T
ENST00000647286.1:n.1660A>T
ENST00000647477.1:n.301A>T
ENST00000399959.6:c.1562A>T	ENSP00000382840.2:p.Asp521Val
ENST00000441189.3:c.341-1071A>T	ENSP00000414281.2:n.341-1071A>T
ENST00000457138.6:c.1514A>T	ENSP00000392494.2:p.Asp505Val
ENST00000478993.5:c.1562A>T	ENSP00000478443.1:p.Asp521Val
ENST00000611968.1:c.4A>T
ENST00000616050.2:c.115A>T
ENST00000625837.2:c.1562A>T	ENSP00000486306.1:p.Asp521Val
ENST00000626301.2:c.1562A>T	ENSP00000486443.1:p.Asp521Val
ENST00000629496.2:c.1562A>T	ENSP00000487224.1:p.Asp521Val
ENST00000629785.2:c.1562A>T	ENSP00000486516.1:p.Asp521Val
ENST00000630255.2:c.1562A>T	ENSP00000486720.1:p.Asp521Val
ENST00000630370.2:c.1562A>T	ENSP00000487062.1:p.Asp521Val
ENST00000630858.2:c.1562A>T	ENSP00000486514.1:p.Asp521Val
NM_001193416.2:c.1562A>T	NP_001180345.1:p.Asp521Val
NM_001193417.2:c.1514A>T	NP_001180346.1:p.Asp505Val
NM_001356.4:c.1562A>T	NP_001347.3:p.Asp521Val
NR_126093.1:n.2507A>T
XM_011543892.1:c.1562A>T	XP_011542194.1:p.Asp521Val
NM_001363819.1:c.1004A>T	NP_001350748.1:p.Asp335Val
XM_011543892.2:c.1562A>T	XP_011542194.1:p.Asp521Val
XM_017029313.1:c.1004A>T	XP_016884802.1:p.Asp335Val
NM_001193416.3:c.1562A>T	NP_001180345.1:p.Asp521Val
NM_001193417.3:c.1514A>T	NP_001180346.1:p.Asp505Val
NM_001356.5:c.1562A>T MANE Select	NP_001347.3:p.Asp521Val