Canonical Allele Identifier: CA412776808

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205840A>T (hg19) ; chrX:g.41346587A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346587A>T , CM000685.2:g.41346587A>T	GRCh38
NC_000023.10:g.41205840A>T , CM000685.1:g.41205840A>T	GRCh37
NC_000023.9:g.41090784A>T	NCBI36
NG_012830.1:g.18190A>T
NG_012830.2:g.18190A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1712A>T	ENSP00000496052.2:p.His571Leu
ENST00000399959.7:c.1577A>T	ENSP00000382840.3:p.His526Leu
ENST00000441189.4:c.1481A>T	ENSP00000414281.3:p.His494Leu
ENST00000457138.7:c.1532A>T	ENSP00000392494.2:p.His511Leu
ENST00000611968.2:c.174A>T
ENST00000616050.3:c.328A>T
ENST00000629496.3:c.1580A>T	ENSP00000487224.1:p.His527Leu
ENST00000642161.1:n.3779A>T
ENST00000642322.1:c.1022A>T	ENSP00000496052.1:p.His341Leu
ENST00000642424.1:c.1022A>T	ENSP00000496356.1:p.His341Leu
ENST00000642589.1:n.4902A>T
ENST00000642597.1:n.1754A>T
ENST00000642687.1:n.1613A>T
ENST00000642722.1:n.2413A>T
ENST00000642763.1:n.2471A>T
ENST00000642793.1:c.*1029A>T	ENSP00000493976.1:n.*1029A>T
ENST00000642801.1:n.1229A>T
ENST00000643820.1:n.950A>T
ENST00000643963.1:c.*862A>T	ENSP00000495264.1:n.*862A>T
ENST00000644073.1:c.1538A>T	ENSP00000493475.1:p.His513Leu
ENST00000644074.1:c.1577A>T	ENSP00000496663.1:p.His526Leu
ENST00000644109.1:c.1742A>T	ENSP00000494952.1:p.His581Leu
ENST00000644307.1:n.1750A>T
ENST00000644513.1:c.1580A>T	ENSP00000493819.1:p.His527Leu
ENST00000644677.1:c.1463A>T	ENSP00000496524.1:p.His488Leu
ENST00000644876.2:c.1580A>T MANE Select	ENSP00000494040.1:p.His527Leu
ENST00000644958.1:n.3241A>T
ENST00000645080.1:c.*2802A>T	ENSP00000494767.1:n.*2802A>T
ENST00000645120.1:n.3075A>T
ENST00000645338.1:n.1750A>T
ENST00000645380.1:n.3044A>T
ENST00000645561.1:n.2756A>T
ENST00000645574.1:n.4444A>T
ENST00000645589.1:c.*79A>T	ENSP00000494588.1:n.*79A>T
ENST00000646107.1:c.1463A>T	ENSP00000494518.1:p.His488Leu
ENST00000646122.1:c.1580A>T	ENSP00000496222.1:p.His527Leu
ENST00000646196.1:n.2549A>T
ENST00000646223.1:c.*1573A>T	ENSP00000496043.1:n.*1573A>T
ENST00000646319.1:c.1580A>T	ENSP00000495377.1:p.His527Leu
ENST00000646390.1:n.3868A>T
ENST00000646627.1:c.1022A>T	ENSP00000493795.1:p.His341Leu
ENST00000646679.1:c.1022A>T	ENSP00000494887.1:p.His341Leu
ENST00000646822.1:n.2642A>T
ENST00000646940.1:n.1754A>T
ENST00000647286.1:n.1678A>T
ENST00000647477.1:n.319A>T
ENST00000399959.6:c.1580A>T	ENSP00000382840.2:p.His527Leu
ENST00000441189.3:c.341-1053A>T	ENSP00000414281.2:n.341-1053A>T
ENST00000457138.6:c.1532A>T	ENSP00000392494.2:p.His511Leu
ENST00000478993.5:c.1580A>T	ENSP00000478443.1:p.His527Leu
ENST00000611968.1:c.22A>T
ENST00000616050.2:c.133A>T
ENST00000625837.2:c.1580A>T	ENSP00000486306.1:p.His527Leu
ENST00000626301.2:c.1580A>T	ENSP00000486443.1:p.His527Leu
ENST00000629496.2:c.1580A>T	ENSP00000487224.1:p.His527Leu
ENST00000629785.2:c.1580A>T	ENSP00000486516.1:p.His527Leu
ENST00000630255.2:c.1580A>T	ENSP00000486720.1:p.His527Leu
ENST00000630370.2:c.1580A>T	ENSP00000487062.1:p.His527Leu
ENST00000630858.2:c.1580A>T	ENSP00000486514.1:p.His527Leu
NM_001193416.2:c.1580A>T	NP_001180345.1:p.His527Leu
NM_001193417.2:c.1532A>T	NP_001180346.1:p.His511Leu
NM_001356.4:c.1580A>T	NP_001347.3:p.His527Leu
NR_126093.1:n.2525A>T
XM_011543892.1:c.1580A>T	XP_011542194.1:p.His527Leu
NM_001363819.1:c.1022A>T	NP_001350748.1:p.His341Leu
XM_011543892.2:c.1580A>T	XP_011542194.1:p.His527Leu
XM_017029313.1:c.1022A>T	XP_016884802.1:p.His341Leu
NM_001193416.3:c.1580A>T	NP_001180345.1:p.His527Leu
NM_001193417.3:c.1532A>T	NP_001180346.1:p.His511Leu
NM_001356.5:c.1580A>T MANE Select	NP_001347.3:p.His527Leu