Canonical Allele Identifier: CA412771518

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204560T>G (hg19) ; chrX:g.41345307T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345307T>G , CM000685.2:g.41345307T>G	GRCh38
NC_000023.10:g.41204560T>G , CM000685.1:g.41204560T>G	GRCh37
NC_000023.9:g.41089504T>G	NCBI36
NG_012830.1:g.16910T>G
NG_012830.2:g.16910T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1285T>G	ENSP00000496052.2:p.Phe429Val
ENST00000399959.7:c.1150T>G	ENSP00000382840.3:p.Phe384Val
ENST00000441189.4:c.1054T>G	ENSP00000414281.3:p.Phe352Val
ENST00000457138.7:c.1105T>G	ENSP00000392494.2:p.Phe369Val
ENST00000629496.3:c.1153T>G	ENSP00000487224.1:p.Phe385Val
ENST00000642161.1:n.3352T>G
ENST00000642322.1:c.595T>G	ENSP00000496052.1:p.Phe199Val
ENST00000642424.1:c.595T>G	ENSP00000496356.1:p.Phe199Val
ENST00000642589.1:n.4475T>G
ENST00000642597.1:n.1327T>G
ENST00000642687.1:n.1186T>G
ENST00000642722.1:n.1986T>G
ENST00000642763.1:n.2044T>G
ENST00000642793.1:c.*602T>G	ENSP00000493976.1:n.*602T>G
ENST00000642801.1:n.802T>G
ENST00000643820.1:n.429T>G
ENST00000643963.1:c.*435T>G	ENSP00000495264.1:n.*435T>G
ENST00000644073.1:c.1111T>G	ENSP00000493475.1:p.Phe371Val
ENST00000644074.1:c.1150T>G	ENSP00000496663.1:p.Phe384Val
ENST00000644109.1:c.1315T>G	ENSP00000494952.1:p.Phe439Val
ENST00000644307.1:n.1244T>G
ENST00000644513.1:c.1153T>G	ENSP00000493819.1:p.Phe385Val
ENST00000644677.1:c.1036T>G	ENSP00000496524.1:p.Phe346Val
ENST00000644876.2:c.1153T>G MANE Select	ENSP00000494040.1:p.Phe385Val
ENST00000644958.1:n.2814T>G
ENST00000645080.1:c.*2375T>G	ENSP00000494767.1:n.*2375T>G
ENST00000645120.1:n.2648T>G
ENST00000645338.1:n.1244T>G
ENST00000645380.1:n.2538T>G
ENST00000645561.1:n.2329T>G
ENST00000645574.1:n.4017T>G
ENST00000645589.1:c.1153T>G	ENSP00000494588.1:p.Phe385Val
ENST00000646093.1:n.337T>G
ENST00000646107.1:c.1036T>G	ENSP00000494518.1:p.Phe346Val
ENST00000646122.1:c.1153T>G	ENSP00000496222.1:p.Phe385Val
ENST00000646196.1:n.2122T>G
ENST00000646223.1:c.*1146T>G	ENSP00000496043.1:n.*1146T>G
ENST00000646319.1:c.1153T>G	ENSP00000495377.1:p.Phe385Val
ENST00000646390.1:n.3441T>G
ENST00000646627.1:c.595T>G	ENSP00000493795.1:p.Phe199Val
ENST00000646679.1:c.595T>G	ENSP00000494887.1:p.Phe199Val
ENST00000646822.1:n.2215T>G
ENST00000646940.1:n.1327T>G
ENST00000647286.1:n.1251T>G
ENST00000399959.6:c.1153T>G	ENSP00000382840.2:p.Phe385Val
ENST00000441189.3:c.341-2333T>G	ENSP00000414281.2:n.341-2333T>G
ENST00000457138.6:c.1105T>G	ENSP00000392494.2:p.Phe369Val
ENST00000478993.5:c.1153T>G	ENSP00000478443.1:p.Phe385Val
ENST00000542215.5:n.1201T>G
ENST00000625837.2:c.1153T>G	ENSP00000486306.1:p.Phe385Val
ENST00000626301.2:c.1153T>G	ENSP00000486443.1:p.Phe385Val
ENST00000629496.2:c.1153T>G	ENSP00000487224.1:p.Phe385Val
ENST00000629785.2:c.1153T>G	ENSP00000486516.1:p.Phe385Val
ENST00000630255.2:c.1153T>G	ENSP00000486720.1:p.Phe385Val
ENST00000630370.2:c.1153T>G	ENSP00000487062.1:p.Phe385Val
ENST00000630858.2:c.1153T>G	ENSP00000486514.1:p.Phe385Val
NM_001193416.2:c.1153T>G	NP_001180345.1:p.Phe385Val
NM_001193417.2:c.1105T>G	NP_001180346.1:p.Phe369Val
NM_001356.4:c.1153T>G	NP_001347.3:p.Phe385Val
NR_126093.1:n.2098T>G
XM_011543892.1:c.1153T>G	XP_011542194.1:p.Phe385Val
NM_001363819.1:c.595T>G	NP_001350748.1:p.Phe199Val
XM_011543892.2:c.1153T>G	XP_011542194.1:p.Phe385Val
XM_017029313.1:c.595T>G	XP_016884802.1:p.Phe199Val
NM_001193416.3:c.1153T>G	NP_001180345.1:p.Phe385Val
NM_001193417.3:c.1105T>G	NP_001180346.1:p.Phe369Val
NM_001356.5:c.1153T>G MANE Select	NP_001347.3:p.Phe385Val