Canonical Allele Identifier: CA515972670

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205763A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346510A>T , CM000685.2:g.41346510A>T	GRCh38
NC_000023.10:g.41205763A>T , CM000685.1:g.41205763A>T	GRCh37
NC_000023.9:g.41090707A>T	NCBI36
NG_012830.1:g.18113A>T
NG_012830.2:g.18113A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1635A>T	ENSP00000496052.2:p.Ala545=
ENST00000399959.7:c.1500A>T	ENSP00000382840.3:p.Ala500=
ENST00000441189.4:c.1404A>T	ENSP00000414281.3:p.Ala468=
ENST00000457138.7:c.1455A>T	ENSP00000392494.2:p.Ala485=
ENST00000611968.2:c.97A>T
ENST00000616050.3:c.251A>T
ENST00000629496.3:c.1503A>T	ENSP00000487224.1:p.Ala501=
ENST00000642161.1:n.3702A>T
ENST00000642322.1:c.945A>T	ENSP00000496052.1:p.Ala315=
ENST00000642424.1:c.945A>T	ENSP00000496356.1:p.Ala315=
ENST00000642589.1:n.4825A>T
ENST00000642597.1:n.1677A>T
ENST00000642687.1:n.1536A>T
ENST00000642722.1:n.2336A>T
ENST00000642763.1:n.2394A>T
ENST00000642793.1:c.*952A>T	ENSP00000493976.1:n.*952A>T
ENST00000642801.1:n.1152A>T
ENST00000643820.1:n.873A>T
ENST00000643963.1:c.*785A>T	ENSP00000495264.1:n.*785A>T
ENST00000644073.1:c.1461A>T	ENSP00000493475.1:p.Ala487=
ENST00000644074.1:c.1500A>T	ENSP00000496663.1:p.Ala500=
ENST00000644109.1:c.1665A>T	ENSP00000494952.1:p.Ala555=
ENST00000644307.1:n.1673A>T
ENST00000644513.1:c.1503A>T	ENSP00000493819.1:p.Ala501=
ENST00000644677.1:c.1386A>T	ENSP00000496524.1:p.Ala462=
ENST00000644876.2:c.1503A>T MANE Select	ENSP00000494040.1:p.Ala501=
ENST00000644958.1:n.3164A>T
ENST00000645080.1:c.*2725A>T	ENSP00000494767.1:n.*2725A>T
ENST00000645120.1:n.2998A>T
ENST00000645338.1:n.1673A>T
ENST00000645380.1:n.2967A>T
ENST00000645561.1:n.2679A>T
ENST00000645574.1:n.4367A>T
ENST00000645589.1:c.*2A>T	ENSP00000494588.1:n.*2A>T
ENST00000646107.1:c.1386A>T	ENSP00000494518.1:p.Ala462=
ENST00000646122.1:c.1503A>T	ENSP00000496222.1:p.Ala501=
ENST00000646196.1:n.2472A>T
ENST00000646223.1:c.*1496A>T	ENSP00000496043.1:n.*1496A>T
ENST00000646319.1:c.1503A>T	ENSP00000495377.1:p.Ala501=
ENST00000646390.1:n.3791A>T
ENST00000646627.1:c.945A>T	ENSP00000493795.1:p.Ala315=
ENST00000646679.1:c.945A>T	ENSP00000494887.1:p.Ala315=
ENST00000646822.1:n.2565A>T
ENST00000646940.1:n.1677A>T
ENST00000647286.1:n.1601A>T
ENST00000647477.1:n.242A>T
ENST00000399959.6:c.1503A>T	ENSP00000382840.2:p.Ala501=
ENST00000441189.3:c.341-1130A>T	ENSP00000414281.2:n.341-1130A>T
ENST00000457138.6:c.1455A>T	ENSP00000392494.2:p.Ala485=
ENST00000478993.5:c.1503A>T	ENSP00000478443.1:p.Ala501=
ENST00000542215.5:n.1551A>T
ENST00000616050.2:c.56A>T
ENST00000625837.2:c.1503A>T	ENSP00000486306.1:p.Ala501=
ENST00000626301.2:c.1503A>T	ENSP00000486443.1:p.Ala501=
ENST00000629496.2:c.1503A>T	ENSP00000487224.1:p.Ala501=
ENST00000629785.2:c.1503A>T	ENSP00000486516.1:p.Ala501=
ENST00000630255.2:c.1503A>T	ENSP00000486720.1:p.Ala501=
ENST00000630370.2:c.1503A>T	ENSP00000487062.1:p.Ala501=
ENST00000630858.2:c.1503A>T	ENSP00000486514.1:p.Ala501=
NM_001193416.2:c.1503A>T	NP_001180345.1:p.Ala501=
NM_001193417.2:c.1455A>T	NP_001180346.1:p.Ala485=
NM_001356.4:c.1503A>T	NP_001347.3:p.Ala501=
NR_126093.1:n.2448A>T
XM_011543892.1:c.1503A>T	XP_011542194.1:p.Ala501=
NM_001363819.1:c.945A>T	NP_001350748.1:p.Ala315=
XM_011543892.2:c.1503A>T	XP_011542194.1:p.Ala501=
XM_017029313.1:c.945A>T	XP_016884802.1:p.Ala315=
NM_001193416.3:c.1503A>T	NP_001180345.1:p.Ala501=
NM_001193417.3:c.1455A>T	NP_001180346.1:p.Ala485=
NM_001356.5:c.1503A>T MANE Select	NP_001347.3:p.Ala501=