Canonical Allele Identifier: CA516347370

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41203599A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344346A>T , CM000685.2:g.41344346A>T	GRCh38
NC_000023.10:g.41203599A>T , CM000685.1:g.41203599A>T	GRCh37
NC_000023.9:g.41088543A>T	NCBI36
NG_012830.1:g.15949A>T
NG_012830.2:g.15949A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1104A>T	ENSP00000496052.2:p.Pro368=
ENST00000399959.7:c.969A>T	ENSP00000382840.3:p.Pro323=
ENST00000441189.4:c.873A>T	ENSP00000414281.3:p.Pro291=
ENST00000457138.7:c.924A>T	ENSP00000392494.2:p.Pro308=
ENST00000629496.3:c.972A>T	ENSP00000487224.1:p.Pro324=
ENST00000631641.2:n.1015A>T
ENST00000642161.1:n.3171A>T
ENST00000642322.1:c.414A>T	ENSP00000496052.1:p.Pro138=
ENST00000642424.1:c.414A>T	ENSP00000496356.1:p.Pro138=
ENST00000642589.1:n.4294A>T
ENST00000642597.1:n.1146A>T
ENST00000642687.1:n.1005A>T
ENST00000642722.1:n.1805A>T
ENST00000642763.1:n.1863A>T
ENST00000642793.1:c.*421A>T	ENSP00000493976.1:n.*421A>T
ENST00000642801.1:n.621A>T
ENST00000643820.1:n.248A>T
ENST00000643963.1:c.*254A>T	ENSP00000495264.1:n.*254A>T
ENST00000644073.1:c.930A>T	ENSP00000493475.1:p.Pro310=
ENST00000644074.1:c.969A>T	ENSP00000496663.1:p.Pro323=
ENST00000644109.1:c.969A>T	ENSP00000494952.1:p.Pro323=
ENST00000644307.1:n.1063A>T
ENST00000644513.1:c.972A>T	ENSP00000493819.1:p.Pro324=
ENST00000644677.1:c.855A>T	ENSP00000496524.1:p.Pro285=
ENST00000644876.2:c.972A>T MANE Select	ENSP00000494040.1:p.Pro324=
ENST00000644958.1:n.2633A>T
ENST00000645080.1:c.*2194A>T	ENSP00000494767.1:n.*2194A>T
ENST00000645120.1:n.2467A>T
ENST00000645338.1:n.1063A>T
ENST00000645380.1:n.2357A>T
ENST00000645561.1:n.2148A>T
ENST00000645574.1:n.3836A>T
ENST00000645589.1:c.972A>T	ENSP00000494588.1:p.Pro324=
ENST00000646093.1:n.156A>T
ENST00000646107.1:c.855A>T	ENSP00000494518.1:p.Pro285=
ENST00000646122.1:c.972A>T	ENSP00000496222.1:p.Pro324=
ENST00000646196.1:n.1941A>T
ENST00000646223.1:c.*965A>T	ENSP00000496043.1:n.*965A>T
ENST00000646319.1:c.972A>T	ENSP00000495377.1:p.Pro324=
ENST00000646390.1:n.3260A>T
ENST00000646627.1:c.414A>T	ENSP00000493795.1:p.Pro138=
ENST00000646679.1:c.414A>T	ENSP00000494887.1:p.Pro138=
ENST00000646822.1:n.2034A>T
ENST00000646940.1:n.1146A>T
ENST00000647286.1:n.1070A>T
ENST00000399959.6:c.972A>T	ENSP00000382840.2:p.Pro324=
ENST00000441189.3:c.340+1796A>T	ENSP00000414281.2:n.340+1796A>T
ENST00000457138.6:c.924A>T	ENSP00000392494.2:p.Pro308=
ENST00000478993.5:c.972A>T	ENSP00000478443.1:p.Pro324=
ENST00000542215.5:n.1020A>T
ENST00000625837.2:c.972A>T	ENSP00000486306.1:p.Pro324=
ENST00000626301.2:c.972A>T	ENSP00000486443.1:p.Pro324=
ENST00000629496.2:c.972A>T	ENSP00000487224.1:p.Pro324=
ENST00000629785.2:c.972A>T	ENSP00000486516.1:p.Pro324=
ENST00000630255.2:c.972A>T	ENSP00000486720.1:p.Pro324=
ENST00000630370.2:c.972A>T	ENSP00000487062.1:p.Pro324=
ENST00000630858.2:c.972A>T	ENSP00000486514.1:p.Pro324=
NM_001193416.2:c.972A>T	NP_001180345.1:p.Pro324=
NM_001193417.2:c.924A>T	NP_001180346.1:p.Pro308=
NM_001356.4:c.972A>T	NP_001347.3:p.Pro324=
NR_126093.1:n.1917A>T
XM_011543892.1:c.972A>T	XP_011542194.1:p.Pro324=
NM_001363819.1:c.414A>T	NP_001350748.1:p.Pro138=
XM_011543892.2:c.972A>T	XP_011542194.1:p.Pro324=
XM_017029313.1:c.414A>T	XP_016884802.1:p.Pro138=
NM_001193416.3:c.972A>T	NP_001180345.1:p.Pro324=
NM_001193417.3:c.924A>T	NP_001180346.1:p.Pro308=
NM_001356.5:c.972A>T MANE Select	NP_001347.3:p.Pro324=