Canonical Allele Identifier: CA516347418

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205784A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346531A>T , CM000685.2:g.41346531A>T	GRCh38
NC_000023.10:g.41205784A>T , CM000685.1:g.41205784A>T	GRCh37
NC_000023.9:g.41090728A>T	NCBI36
NG_012830.1:g.18134A>T
NG_012830.2:g.18134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1656A>T	ENSP00000496052.2:p.Ser552=
ENST00000399959.7:c.1521A>T	ENSP00000382840.3:p.Ser507=
ENST00000441189.4:c.1425A>T	ENSP00000414281.3:p.Ser475=
ENST00000457138.7:c.1476A>T	ENSP00000392494.2:p.Ser492=
ENST00000611968.2:c.118A>T
ENST00000616050.3:c.272A>T
ENST00000629496.3:c.1524A>T	ENSP00000487224.1:p.Ser508=
ENST00000642161.1:n.3723A>T
ENST00000642322.1:c.966A>T	ENSP00000496052.1:p.Ser322=
ENST00000642424.1:c.966A>T	ENSP00000496356.1:p.Ser322=
ENST00000642589.1:n.4846A>T
ENST00000642597.1:n.1698A>T
ENST00000642687.1:n.1557A>T
ENST00000642722.1:n.2357A>T
ENST00000642763.1:n.2415A>T
ENST00000642793.1:c.*973A>T	ENSP00000493976.1:n.*973A>T
ENST00000642801.1:n.1173A>T
ENST00000643820.1:n.894A>T
ENST00000643963.1:c.*806A>T	ENSP00000495264.1:n.*806A>T
ENST00000644073.1:c.1482A>T	ENSP00000493475.1:p.Ser494=
ENST00000644074.1:c.1521A>T	ENSP00000496663.1:p.Ser507=
ENST00000644109.1:c.1686A>T	ENSP00000494952.1:p.Ser562=
ENST00000644307.1:n.1694A>T
ENST00000644513.1:c.1524A>T	ENSP00000493819.1:p.Ser508=
ENST00000644677.1:c.1407A>T	ENSP00000496524.1:p.Ser469=
ENST00000644876.2:c.1524A>T MANE Select	ENSP00000494040.1:p.Ser508=
ENST00000644958.1:n.3185A>T
ENST00000645080.1:c.*2746A>T	ENSP00000494767.1:n.*2746A>T
ENST00000645120.1:n.3019A>T
ENST00000645338.1:n.1694A>T
ENST00000645380.1:n.2988A>T
ENST00000645561.1:n.2700A>T
ENST00000645574.1:n.4388A>T
ENST00000645589.1:c.*23A>T	ENSP00000494588.1:n.*23A>T
ENST00000646107.1:c.1407A>T	ENSP00000494518.1:p.Ser469=
ENST00000646122.1:c.1524A>T	ENSP00000496222.1:p.Ser508=
ENST00000646196.1:n.2493A>T
ENST00000646223.1:c.*1517A>T	ENSP00000496043.1:n.*1517A>T
ENST00000646319.1:c.1524A>T	ENSP00000495377.1:p.Ser508=
ENST00000646390.1:n.3812A>T
ENST00000646627.1:c.966A>T	ENSP00000493795.1:p.Ser322=
ENST00000646679.1:c.966A>T	ENSP00000494887.1:p.Ser322=
ENST00000646822.1:n.2586A>T
ENST00000646940.1:n.1698A>T
ENST00000647286.1:n.1622A>T
ENST00000647477.1:n.263A>T
ENST00000399959.6:c.1524A>T	ENSP00000382840.2:p.Ser508=
ENST00000441189.3:c.341-1109A>T	ENSP00000414281.2:n.341-1109A>T
ENST00000457138.6:c.1476A>T	ENSP00000392494.2:p.Ser492=
ENST00000478993.5:c.1524A>T	ENSP00000478443.1:p.Ser508=
ENST00000542215.5:n.1572A>T
ENST00000616050.2:c.77A>T
ENST00000625837.2:c.1524A>T	ENSP00000486306.1:p.Ser508=
ENST00000626301.2:c.1524A>T	ENSP00000486443.1:p.Ser508=
ENST00000629496.2:c.1524A>T	ENSP00000487224.1:p.Ser508=
ENST00000629785.2:c.1524A>T	ENSP00000486516.1:p.Ser508=
ENST00000630255.2:c.1524A>T	ENSP00000486720.1:p.Ser508=
ENST00000630370.2:c.1524A>T	ENSP00000487062.1:p.Ser508=
ENST00000630858.2:c.1524A>T	ENSP00000486514.1:p.Ser508=
NM_001193416.2:c.1524A>T	NP_001180345.1:p.Ser508=
NM_001193417.2:c.1476A>T	NP_001180346.1:p.Ser492=
NM_001356.4:c.1524A>T	NP_001347.3:p.Ser508=
NR_126093.1:n.2469A>T
XM_011543892.1:c.1524A>T	XP_011542194.1:p.Ser508=
NM_001363819.1:c.966A>T	NP_001350748.1:p.Ser322=
XM_011543892.2:c.1524A>T	XP_011542194.1:p.Ser508=
XM_017029313.1:c.966A>T	XP_016884802.1:p.Ser322=
NM_001193416.3:c.1524A>T	NP_001180345.1:p.Ser508=
NM_001193417.3:c.1476A>T	NP_001180346.1:p.Ser492=
NM_001356.5:c.1524A>T MANE Select	NP_001347.3:p.Ser508=