Canonical Allele Identifier: CA2425881507

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346599G= , CM000685.2:g.41346599G=	GRCh38
NC_000023.10:g.41205852G= , CM000685.1:g.41205852G=	GRCh37
NC_000023.9:g.41090796G=	NCBI36
NG_012830.1:g.18202G=
NG_012830.2:g.18202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1724G=	ENSP00000496052.2:p.Arg575=
ENST00000399959.7:c.1589G=	ENSP00000382840.3:p.Arg530=
ENST00000441189.4:c.1493G=	ENSP00000414281.3:p.Arg498=
ENST00000457138.7:c.1544G=	ENSP00000392494.2:p.Arg515=
ENST00000611968.2:c.186G=
ENST00000616050.3:c.340G=
ENST00000629496.3:c.1592G=	ENSP00000487224.1:p.Arg531=
ENST00000642161.1:n.3791G=
ENST00000642322.1:c.1034G=	ENSP00000496052.1:p.Arg345=
ENST00000642424.1:c.1034G=	ENSP00000496356.1:p.Arg345=
ENST00000642589.1:n.4914G=
ENST00000642597.1:n.1766G=
ENST00000642687.1:n.1625G=
ENST00000642722.1:n.2425G=
ENST00000642763.1:n.2483G=
ENST00000642793.1:c.*1041G=	ENSP00000493976.1:n.*1041G=
ENST00000642801.1:n.1241G=
ENST00000643820.1:n.962G=
ENST00000643963.1:c.*874G=	ENSP00000495264.1:n.*874G=
ENST00000644073.1:c.1550G=	ENSP00000493475.1:p.Arg517=
ENST00000644074.1:c.1589G=	ENSP00000496663.1:p.Arg530=
ENST00000644109.1:c.1754G=	ENSP00000494952.1:p.Arg585=
ENST00000644307.1:n.1762G=
ENST00000644513.1:c.1592G=	ENSP00000493819.1:p.Arg531=
ENST00000644677.1:c.1475G=	ENSP00000496524.1:p.Arg492=
ENST00000644876.2:c.1592G= MANE Select	ENSP00000494040.1:p.Arg531=
ENST00000644958.1:n.3253G=
ENST00000645080.1:c.*2814G=	ENSP00000494767.1:n.*2814G=
ENST00000645120.1:n.3087G=
ENST00000645338.1:n.1762G=
ENST00000645380.1:n.3056G=
ENST00000645561.1:n.2768G=
ENST00000645574.1:n.4456G=
ENST00000645589.1:c.*91G=	ENSP00000494588.1:n.*91G=
ENST00000646107.1:c.1475G=	ENSP00000494518.1:p.Arg492=
ENST00000646122.1:c.1592G=	ENSP00000496222.1:p.Arg531=
ENST00000646196.1:n.2561G=
ENST00000646223.1:c.*1585G=	ENSP00000496043.1:n.*1585G=
ENST00000646319.1:c.1592G=	ENSP00000495377.1:p.Arg531=
ENST00000646390.1:n.3880G=
ENST00000646627.1:c.1034G=	ENSP00000493795.1:p.Arg345=
ENST00000646679.1:c.1034G=	ENSP00000494887.1:p.Arg345=
ENST00000646822.1:n.2654G=
ENST00000646940.1:n.1766G=
ENST00000647286.1:n.1690G=
ENST00000647477.1:n.331G=
ENST00000399959.6:c.1592G=	ENSP00000382840.2:p.Arg531=
ENST00000441189.3:c.341-1041G=	ENSP00000414281.2:n.341-1041G=
ENST00000457138.6:c.1544G=	ENSP00000392494.2:p.Arg515=
ENST00000478993.5:c.1592G=	ENSP00000478443.1:p.Arg531=
ENST00000611968.1:c.34G=
ENST00000616050.2:c.145G=
ENST00000625837.2:c.1592G=	ENSP00000486306.1:p.Arg531=
ENST00000626301.2:c.1592G=	ENSP00000486443.1:p.Arg531=
ENST00000629496.2:c.1592G=	ENSP00000487224.1:p.Arg531=
ENST00000629785.2:c.1592G=	ENSP00000486516.1:p.Arg531=
ENST00000630255.2:c.1592G=	ENSP00000486720.1:p.Arg531=
ENST00000630370.2:c.1592G=	ENSP00000487062.1:p.Arg531=
ENST00000630858.2:c.1592G=	ENSP00000486514.1:p.Arg531=
NM_001193416.2:c.1592G=	NP_001180345.1:p.Arg531=
NM_001193417.2:c.1544G=	NP_001180346.1:p.Arg515=
NM_001356.4:c.1592G=	NP_001347.3:p.Arg531=
NR_126093.1:n.2537G=
XM_011543892.1:c.1592G=	XP_011542194.1:p.Arg531=
NM_001363819.1:c.1034G=	NP_001350748.1:p.Arg345=
XM_011543892.2:c.1592G=	XP_011542194.1:p.Arg531=
XM_017029313.1:c.1034G=	XP_016884802.1:p.Arg345=
NM_001193416.3:c.1592G=	NP_001180345.1:p.Arg531=
NM_001193417.3:c.1544G=	NP_001180346.1:p.Arg515=
NM_001356.5:c.1592G= MANE Select	NP_001347.3:p.Arg531=