Canonical Allele Identifier: CA412775417

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205600G>C (hg19) ; chrX:g.41346347G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346347G>C , CM000685.2:g.41346347G>C	GRCh38
NC_000023.10:g.41205600G>C , CM000685.1:g.41205600G>C	GRCh37
NC_000023.9:g.41090544G>C	NCBI36
NG_012830.1:g.17950G>C
NG_012830.2:g.17950G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1566G>C	ENSP00000496052.2:p.Arg522Ser
ENST00000399959.7:c.1431G>C	ENSP00000382840.3:p.Arg477Ser
ENST00000441189.4:c.1335G>C	ENSP00000414281.3:p.Arg445Ser
ENST00000457138.7:c.1386G>C	ENSP00000392494.2:p.Arg462Ser
ENST00000611968.2:c.28G>C
ENST00000616050.3:c.182G>C
ENST00000629496.3:c.1434G>C	ENSP00000487224.1:p.Arg478Ser
ENST00000642161.1:n.3633G>C
ENST00000642322.1:c.876G>C	ENSP00000496052.1:p.Arg292Ser
ENST00000642424.1:c.876G>C	ENSP00000496356.1:p.Arg292Ser
ENST00000642589.1:n.4756G>C
ENST00000642597.1:n.1608G>C
ENST00000642687.1:n.1467G>C
ENST00000642722.1:n.2267G>C
ENST00000642763.1:n.2325G>C
ENST00000642793.1:c.*883G>C	ENSP00000493976.1:n.*883G>C
ENST00000642801.1:n.1083G>C
ENST00000643820.1:n.710G>C
ENST00000643963.1:c.*716G>C	ENSP00000495264.1:n.*716G>C
ENST00000644073.1:c.1392G>C	ENSP00000493475.1:p.Arg464Ser
ENST00000644074.1:c.1431G>C	ENSP00000496663.1:p.Arg477Ser
ENST00000644109.1:c.1596G>C	ENSP00000494952.1:p.Arg532Ser
ENST00000644307.1:n.1604G>C
ENST00000644513.1:c.1434G>C	ENSP00000493819.1:p.Arg478Ser
ENST00000644677.1:c.1317G>C	ENSP00000496524.1:p.Arg439Ser
ENST00000644876.2:c.1434G>C MANE Select	ENSP00000494040.1:p.Arg478Ser
ENST00000644958.1:n.3095G>C
ENST00000645080.1:c.*2656G>C	ENSP00000494767.1:n.*2656G>C
ENST00000645120.1:n.2929G>C
ENST00000645338.1:n.1604G>C
ENST00000645380.1:n.2898G>C
ENST00000645561.1:n.2610G>C
ENST00000645574.1:n.4298G>C
ENST00000645589.1:c.1434G>C	ENSP00000494588.1:p.Arg478Ser
ENST00000646107.1:c.1317G>C	ENSP00000494518.1:p.Arg439Ser
ENST00000646122.1:c.1434G>C	ENSP00000496222.1:p.Arg478Ser
ENST00000646196.1:n.2403G>C
ENST00000646223.1:c.*1427G>C	ENSP00000496043.1:n.*1427G>C
ENST00000646319.1:c.1434G>C	ENSP00000495377.1:p.Arg478Ser
ENST00000646390.1:n.3722G>C
ENST00000646627.1:c.876G>C	ENSP00000493795.1:p.Arg292Ser
ENST00000646679.1:c.876G>C	ENSP00000494887.1:p.Arg292Ser
ENST00000646822.1:n.2496G>C
ENST00000646940.1:n.1608G>C
ENST00000647286.1:n.1532G>C
ENST00000647477.1:n.173G>C
ENST00000399959.6:c.1434G>C	ENSP00000382840.2:p.Arg478Ser
ENST00000441189.3:c.341-1293G>C	ENSP00000414281.2:n.341-1293G>C
ENST00000457138.6:c.1386G>C	ENSP00000392494.2:p.Arg462Ser
ENST00000478993.5:c.1434G>C	ENSP00000478443.1:p.Arg478Ser
ENST00000542215.5:n.1482G>C
ENST00000625837.2:c.1434G>C	ENSP00000486306.1:p.Arg478Ser
ENST00000626301.2:c.1434G>C	ENSP00000486443.1:p.Arg478Ser
ENST00000629496.2:c.1434G>C	ENSP00000487224.1:p.Arg478Ser
ENST00000629785.2:c.1434G>C	ENSP00000486516.1:p.Arg478Ser
ENST00000630255.2:c.1434G>C	ENSP00000486720.1:p.Arg478Ser
ENST00000630370.2:c.1434G>C	ENSP00000487062.1:p.Arg478Ser
ENST00000630858.2:c.1434G>C	ENSP00000486514.1:p.Arg478Ser
NM_001193416.2:c.1434G>C	NP_001180345.1:p.Arg478Ser
NM_001193417.2:c.1386G>C	NP_001180346.1:p.Arg462Ser
NM_001356.4:c.1434G>C	NP_001347.3:p.Arg478Ser
NR_126093.1:n.2379G>C
XM_011543892.1:c.1434G>C	XP_011542194.1:p.Arg478Ser
NM_001363819.1:c.876G>C	NP_001350748.1:p.Arg292Ser
XM_011543892.2:c.1434G>C	XP_011542194.1:p.Arg478Ser
XM_017029313.1:c.876G>C	XP_016884802.1:p.Arg292Ser
NM_001193416.3:c.1434G>C	NP_001180345.1:p.Arg478Ser
NM_001193417.3:c.1386G>C	NP_001180346.1:p.Arg462Ser
NM_001356.5:c.1434G>C MANE Select	NP_001347.3:p.Arg478Ser