Canonical Allele Identifier: CA515972406

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205546C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346293C>T , CM000685.2:g.41346293C>T	GRCh38
NC_000023.10:g.41205546C>T , CM000685.1:g.41205546C>T	GRCh37
NC_000023.9:g.41090490C>T	NCBI36
NG_012830.1:g.17896C>T
NG_012830.2:g.17896C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1512C>T	ENSP00000496052.2:p.Phe504=
ENST00000399959.7:c.1377C>T	ENSP00000382840.3:p.Phe459=
ENST00000441189.4:c.1281C>T	ENSP00000414281.3:p.Phe427=
ENST00000457138.7:c.1332C>T	ENSP00000392494.2:p.Phe444=
ENST00000616050.3:c.128C>T
ENST00000629496.3:c.1380C>T	ENSP00000487224.1:p.Phe460=
ENST00000642161.1:n.3579C>T
ENST00000642322.1:c.822C>T	ENSP00000496052.1:p.Phe274=
ENST00000642424.1:c.822C>T	ENSP00000496356.1:p.Phe274=
ENST00000642589.1:n.4702C>T
ENST00000642597.1:n.1554C>T
ENST00000642687.1:n.1413C>T
ENST00000642722.1:n.2213C>T
ENST00000642763.1:n.2271C>T
ENST00000642793.1:c.*829C>T	ENSP00000493976.1:n.*829C>T
ENST00000642801.1:n.1029C>T
ENST00000643820.1:n.656C>T
ENST00000643963.1:c.*662C>T	ENSP00000495264.1:n.*662C>T
ENST00000644073.1:c.1338C>T	ENSP00000493475.1:p.Phe446=
ENST00000644074.1:c.1377C>T	ENSP00000496663.1:p.Phe459=
ENST00000644109.1:c.1542C>T	ENSP00000494952.1:p.Phe514=
ENST00000644307.1:n.1550C>T
ENST00000644513.1:c.1380C>T	ENSP00000493819.1:p.Phe460=
ENST00000644677.1:c.1263C>T	ENSP00000496524.1:p.Phe421=
ENST00000644876.2:c.1380C>T MANE Select	ENSP00000494040.1:p.Phe460=
ENST00000644958.1:n.3041C>T
ENST00000645080.1:c.*2602C>T	ENSP00000494767.1:n.*2602C>T
ENST00000645120.1:n.2875C>T
ENST00000645338.1:n.1550C>T
ENST00000645380.1:n.2844C>T
ENST00000645561.1:n.2556C>T
ENST00000645574.1:n.4244C>T
ENST00000645589.1:c.1380C>T	ENSP00000494588.1:p.Phe460=
ENST00000646107.1:c.1263C>T	ENSP00000494518.1:p.Phe421=
ENST00000646122.1:c.1380C>T	ENSP00000496222.1:p.Phe460=
ENST00000646196.1:n.2349C>T
ENST00000646223.1:c.*1373C>T	ENSP00000496043.1:n.*1373C>T
ENST00000646319.1:c.1380C>T	ENSP00000495377.1:p.Phe460=
ENST00000646390.1:n.3668C>T
ENST00000646627.1:c.822C>T	ENSP00000493795.1:p.Phe274=
ENST00000646679.1:c.822C>T	ENSP00000494887.1:p.Phe274=
ENST00000646822.1:n.2442C>T
ENST00000646940.1:n.1554C>T
ENST00000647286.1:n.1478C>T
ENST00000647477.1:n.119C>T
ENST00000399959.6:c.1380C>T	ENSP00000382840.2:p.Phe460=
ENST00000441189.3:c.341-1347C>T	ENSP00000414281.2:n.341-1347C>T
ENST00000457138.6:c.1332C>T	ENSP00000392494.2:p.Phe444=
ENST00000478993.5:c.1380C>T	ENSP00000478443.1:p.Phe460=
ENST00000542215.5:n.1428C>T
ENST00000625837.2:c.1380C>T	ENSP00000486306.1:p.Phe460=
ENST00000626301.2:c.1380C>T	ENSP00000486443.1:p.Phe460=
ENST00000629496.2:c.1380C>T	ENSP00000487224.1:p.Phe460=
ENST00000629785.2:c.1380C>T	ENSP00000486516.1:p.Phe460=
ENST00000630255.2:c.1380C>T	ENSP00000486720.1:p.Phe460=
ENST00000630370.2:c.1380C>T	ENSP00000487062.1:p.Phe460=
ENST00000630858.2:c.1380C>T	ENSP00000486514.1:p.Phe460=
NM_001193416.2:c.1380C>T	NP_001180345.1:p.Phe460=
NM_001193417.2:c.1332C>T	NP_001180346.1:p.Phe444=
NM_001356.4:c.1380C>T	NP_001347.3:p.Phe460=
NR_126093.1:n.2325C>T
XM_011543892.1:c.1380C>T	XP_011542194.1:p.Phe460=
NM_001363819.1:c.822C>T	NP_001350748.1:p.Phe274=
XM_011543892.2:c.1380C>T	XP_011542194.1:p.Phe460=
XM_017029313.1:c.822C>T	XP_016884802.1:p.Phe274=
NM_001193416.3:c.1380C>T	NP_001180345.1:p.Phe460=
NM_001193417.3:c.1332C>T	NP_001180346.1:p.Phe444=
NM_001356.5:c.1380C>T MANE Select	NP_001347.3:p.Phe460=