Canonical Allele Identifier: CA412776627

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205816C>T (hg19) ; chrX:g.41346563C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346563C>T , CM000685.2:g.41346563C>T	GRCh38
NC_000023.10:g.41205816C>T , CM000685.1:g.41205816C>T	GRCh37
NC_000023.9:g.41090760C>T	NCBI36
NG_012830.1:g.18166C>T
NG_012830.2:g.18166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1688C>T	ENSP00000496052.2:p.Pro563Leu
ENST00000399959.7:c.1553C>T	ENSP00000382840.3:p.Pro518Leu
ENST00000441189.4:c.1457C>T	ENSP00000414281.3:p.Pro486Leu
ENST00000457138.7:c.1508C>T	ENSP00000392494.2:p.Pro503Leu
ENST00000611968.2:c.150C>T
ENST00000616050.3:c.304C>T
ENST00000629496.3:c.1556C>T	ENSP00000487224.1:p.Pro519Leu
ENST00000642161.1:n.3755C>T
ENST00000642322.1:c.998C>T	ENSP00000496052.1:p.Pro333Leu
ENST00000642424.1:c.998C>T	ENSP00000496356.1:p.Pro333Leu
ENST00000642589.1:n.4878C>T
ENST00000642597.1:n.1730C>T
ENST00000642687.1:n.1589C>T
ENST00000642722.1:n.2389C>T
ENST00000642763.1:n.2447C>T
ENST00000642793.1:c.*1005C>T	ENSP00000493976.1:n.*1005C>T
ENST00000642801.1:n.1205C>T
ENST00000643820.1:n.926C>T
ENST00000643963.1:c.*838C>T	ENSP00000495264.1:n.*838C>T
ENST00000644073.1:c.1514C>T	ENSP00000493475.1:p.Pro505Leu
ENST00000644074.1:c.1553C>T	ENSP00000496663.1:p.Pro518Leu
ENST00000644109.1:c.1718C>T	ENSP00000494952.1:p.Pro573Leu
ENST00000644307.1:n.1726C>T
ENST00000644513.1:c.1556C>T	ENSP00000493819.1:p.Pro519Leu
ENST00000644677.1:c.1439C>T	ENSP00000496524.1:p.Pro480Leu
ENST00000644876.2:c.1556C>T MANE Select	ENSP00000494040.1:p.Pro519Leu
ENST00000644958.1:n.3217C>T
ENST00000645080.1:c.*2778C>T	ENSP00000494767.1:n.*2778C>T
ENST00000645120.1:n.3051C>T
ENST00000645338.1:n.1726C>T
ENST00000645380.1:n.3020C>T
ENST00000645561.1:n.2732C>T
ENST00000645574.1:n.4420C>T
ENST00000645589.1:c.*55C>T	ENSP00000494588.1:n.*55C>T
ENST00000646107.1:c.1439C>T	ENSP00000494518.1:p.Pro480Leu
ENST00000646122.1:c.1556C>T	ENSP00000496222.1:p.Pro519Leu
ENST00000646196.1:n.2525C>T
ENST00000646223.1:c.*1549C>T	ENSP00000496043.1:n.*1549C>T
ENST00000646319.1:c.1556C>T	ENSP00000495377.1:p.Pro519Leu
ENST00000646390.1:n.3844C>T
ENST00000646627.1:c.998C>T	ENSP00000493795.1:p.Pro333Leu
ENST00000646679.1:c.998C>T	ENSP00000494887.1:p.Pro333Leu
ENST00000646822.1:n.2618C>T
ENST00000646940.1:n.1730C>T
ENST00000647286.1:n.1654C>T
ENST00000647477.1:n.295C>T
ENST00000399959.6:c.1556C>T	ENSP00000382840.2:p.Pro519Leu
ENST00000441189.3:c.341-1077C>T	ENSP00000414281.2:n.341-1077C>T
ENST00000457138.6:c.1508C>T	ENSP00000392494.2:p.Pro503Leu
ENST00000478993.5:c.1556C>T	ENSP00000478443.1:p.Pro519Leu
ENST00000616050.2:c.109C>T
ENST00000625837.2:c.1556C>T	ENSP00000486306.1:p.Pro519Leu
ENST00000626301.2:c.1556C>T	ENSP00000486443.1:p.Pro519Leu
ENST00000629496.2:c.1556C>T	ENSP00000487224.1:p.Pro519Leu
ENST00000629785.2:c.1556C>T	ENSP00000486516.1:p.Pro519Leu
ENST00000630255.2:c.1556C>T	ENSP00000486720.1:p.Pro519Leu
ENST00000630370.2:c.1556C>T	ENSP00000487062.1:p.Pro519Leu
ENST00000630858.2:c.1556C>T	ENSP00000486514.1:p.Pro519Leu
NM_001193416.2:c.1556C>T	NP_001180345.1:p.Pro519Leu
NM_001193417.2:c.1508C>T	NP_001180346.1:p.Pro503Leu
NM_001356.4:c.1556C>T	NP_001347.3:p.Pro519Leu
NR_126093.1:n.2501C>T
XM_011543892.1:c.1556C>T	XP_011542194.1:p.Pro519Leu
NM_001363819.1:c.998C>T	NP_001350748.1:p.Pro333Leu
XM_011543892.2:c.1556C>T	XP_011542194.1:p.Pro519Leu
XM_017029313.1:c.998C>T	XP_016884802.1:p.Pro333Leu
NM_001193416.3:c.1556C>T	NP_001180345.1:p.Pro519Leu
NM_001193417.3:c.1508C>T	NP_001180346.1:p.Pro503Leu
NM_001356.5:c.1556C>T MANE Select	NP_001347.3:p.Pro519Leu