Canonical Allele Identifier: CA516347436

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205817A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346564A>T , CM000685.2:g.41346564A>T	GRCh38
NC_000023.10:g.41205817A>T , CM000685.1:g.41205817A>T	GRCh37
NC_000023.9:g.41090761A>T	NCBI36
NG_012830.1:g.18167A>T
NG_012830.2:g.18167A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1689A>T	ENSP00000496052.2:p.Pro563=
ENST00000399959.7:c.1554A>T	ENSP00000382840.3:p.Pro518=
ENST00000441189.4:c.1458A>T	ENSP00000414281.3:p.Pro486=
ENST00000457138.7:c.1509A>T	ENSP00000392494.2:p.Pro503=
ENST00000611968.2:c.151A>T
ENST00000616050.3:c.305A>T
ENST00000629496.3:c.1557A>T	ENSP00000487224.1:p.Pro519=
ENST00000642161.1:n.3756A>T
ENST00000642322.1:c.999A>T	ENSP00000496052.1:p.Pro333=
ENST00000642424.1:c.999A>T	ENSP00000496356.1:p.Pro333=
ENST00000642589.1:n.4879A>T
ENST00000642597.1:n.1731A>T
ENST00000642687.1:n.1590A>T
ENST00000642722.1:n.2390A>T
ENST00000642763.1:n.2448A>T
ENST00000642793.1:c.*1006A>T	ENSP00000493976.1:n.*1006A>T
ENST00000642801.1:n.1206A>T
ENST00000643820.1:n.927A>T
ENST00000643963.1:c.*839A>T	ENSP00000495264.1:n.*839A>T
ENST00000644073.1:c.1515A>T	ENSP00000493475.1:p.Pro505=
ENST00000644074.1:c.1554A>T	ENSP00000496663.1:p.Pro518=
ENST00000644109.1:c.1719A>T	ENSP00000494952.1:p.Pro573=
ENST00000644307.1:n.1727A>T
ENST00000644513.1:c.1557A>T	ENSP00000493819.1:p.Pro519=
ENST00000644677.1:c.1440A>T	ENSP00000496524.1:p.Pro480=
ENST00000644876.2:c.1557A>T MANE Select	ENSP00000494040.1:p.Pro519=
ENST00000644958.1:n.3218A>T
ENST00000645080.1:c.*2779A>T	ENSP00000494767.1:n.*2779A>T
ENST00000645120.1:n.3052A>T
ENST00000645338.1:n.1727A>T
ENST00000645380.1:n.3021A>T
ENST00000645561.1:n.2733A>T
ENST00000645574.1:n.4421A>T
ENST00000645589.1:c.*56A>T	ENSP00000494588.1:n.*56A>T
ENST00000646107.1:c.1440A>T	ENSP00000494518.1:p.Pro480=
ENST00000646122.1:c.1557A>T	ENSP00000496222.1:p.Pro519=
ENST00000646196.1:n.2526A>T
ENST00000646223.1:c.*1550A>T	ENSP00000496043.1:n.*1550A>T
ENST00000646319.1:c.1557A>T	ENSP00000495377.1:p.Pro519=
ENST00000646390.1:n.3845A>T
ENST00000646627.1:c.999A>T	ENSP00000493795.1:p.Pro333=
ENST00000646679.1:c.999A>T	ENSP00000494887.1:p.Pro333=
ENST00000646822.1:n.2619A>T
ENST00000646940.1:n.1731A>T
ENST00000647286.1:n.1655A>T
ENST00000647477.1:n.296A>T
ENST00000399959.6:c.1557A>T	ENSP00000382840.2:p.Pro519=
ENST00000441189.3:c.341-1076A>T	ENSP00000414281.2:n.341-1076A>T
ENST00000457138.6:c.1509A>T	ENSP00000392494.2:p.Pro503=
ENST00000478993.5:c.1557A>T	ENSP00000478443.1:p.Pro519=
ENST00000616050.2:c.110A>T
ENST00000625837.2:c.1557A>T	ENSP00000486306.1:p.Pro519=
ENST00000626301.2:c.1557A>T	ENSP00000486443.1:p.Pro519=
ENST00000629496.2:c.1557A>T	ENSP00000487224.1:p.Pro519=
ENST00000629785.2:c.1557A>T	ENSP00000486516.1:p.Pro519=
ENST00000630255.2:c.1557A>T	ENSP00000486720.1:p.Pro519=
ENST00000630370.2:c.1557A>T	ENSP00000487062.1:p.Pro519=
ENST00000630858.2:c.1557A>T	ENSP00000486514.1:p.Pro519=
NM_001193416.2:c.1557A>T	NP_001180345.1:p.Pro519=
NM_001193417.2:c.1509A>T	NP_001180346.1:p.Pro503=
NM_001356.4:c.1557A>T	NP_001347.3:p.Pro519=
NR_126093.1:n.2502A>T
XM_011543892.1:c.1557A>T	XP_011542194.1:p.Pro519=
NM_001363819.1:c.999A>T	NP_001350748.1:p.Pro333=
XM_011543892.2:c.1557A>T	XP_011542194.1:p.Pro519=
XM_017029313.1:c.999A>T	XP_016884802.1:p.Pro333=
NM_001193416.3:c.1557A>T	NP_001180345.1:p.Pro519=
NM_001193417.3:c.1509A>T	NP_001180346.1:p.Pro503=
NM_001356.5:c.1557A>T MANE Select	NP_001347.3:p.Pro519=