Canonical Allele Identifier: CA2425881043

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345278T= , CM000685.2:g.41345278T=	GRCh38
NC_000023.10:g.41204531T= , CM000685.1:g.41204531T=	GRCh37
NC_000023.9:g.41089475T=	NCBI36
NG_012830.1:g.16881T=
NG_012830.2:g.16881T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1256T=	ENSP00000496052.2:p.Val419=
ENST00000399959.7:c.1121T=	ENSP00000382840.3:p.Val374=
ENST00000441189.4:c.1025T=	ENSP00000414281.3:p.Val342=
ENST00000457138.7:c.1076T=	ENSP00000392494.2:p.Val359=
ENST00000629496.3:c.1124T=	ENSP00000487224.1:p.Val375=
ENST00000642161.1:n.3323T=
ENST00000642322.1:c.566T=	ENSP00000496052.1:p.Val189=
ENST00000642424.1:c.566T=	ENSP00000496356.1:p.Val189=
ENST00000642589.1:n.4446T=
ENST00000642597.1:n.1298T=
ENST00000642687.1:n.1157T=
ENST00000642722.1:n.1957T=
ENST00000642763.1:n.2015T=
ENST00000642793.1:c.*573T=	ENSP00000493976.1:n.*573T=
ENST00000642801.1:n.773T=
ENST00000643820.1:n.400T=
ENST00000643963.1:c.*406T=	ENSP00000495264.1:n.*406T=
ENST00000644073.1:c.1082T=	ENSP00000493475.1:p.Val361=
ENST00000644074.1:c.1121T=	ENSP00000496663.1:p.Val374=
ENST00000644109.1:c.1286T=	ENSP00000494952.1:p.Val429=
ENST00000644307.1:n.1215T=
ENST00000644513.1:c.1124T=	ENSP00000493819.1:p.Val375=
ENST00000644677.1:c.1007T=	ENSP00000496524.1:p.Val336=
ENST00000644876.2:c.1124T= MANE Select	ENSP00000494040.1:p.Val375=
ENST00000644958.1:n.2785T=
ENST00000645080.1:c.*2346T=	ENSP00000494767.1:n.*2346T=
ENST00000645120.1:n.2619T=
ENST00000645338.1:n.1215T=
ENST00000645380.1:n.2509T=
ENST00000645561.1:n.2300T=
ENST00000645574.1:n.3988T=
ENST00000645589.1:c.1124T=	ENSP00000494588.1:p.Val375=
ENST00000646093.1:n.308T=
ENST00000646107.1:c.1007T=	ENSP00000494518.1:p.Val336=
ENST00000646122.1:c.1124T=	ENSP00000496222.1:p.Val375=
ENST00000646196.1:n.2093T=
ENST00000646223.1:c.*1117T=	ENSP00000496043.1:n.*1117T=
ENST00000646319.1:c.1124T=	ENSP00000495377.1:p.Val375=
ENST00000646390.1:n.3412T=
ENST00000646627.1:c.566T=	ENSP00000493795.1:p.Val189=
ENST00000646679.1:c.566T=	ENSP00000494887.1:p.Val189=
ENST00000646822.1:n.2186T=
ENST00000646940.1:n.1298T=
ENST00000647286.1:n.1222T=
ENST00000399959.6:c.1124T=	ENSP00000382840.2:p.Val375=
ENST00000441189.3:c.341-2362T=	ENSP00000414281.2:n.341-2362T=
ENST00000457138.6:c.1076T=	ENSP00000392494.2:p.Val359=
ENST00000478993.5:c.1124T=	ENSP00000478443.1:p.Val375=
ENST00000542215.5:n.1172T=
ENST00000625837.2:c.1124T=	ENSP00000486306.1:p.Val375=
ENST00000626301.2:c.1124T=	ENSP00000486443.1:p.Val375=
ENST00000629496.2:c.1124T=	ENSP00000487224.1:p.Val375=
ENST00000629785.2:c.1124T=	ENSP00000486516.1:p.Val375=
ENST00000630255.2:c.1124T=	ENSP00000486720.1:p.Val375=
ENST00000630370.2:c.1124T=	ENSP00000487062.1:p.Val375=
ENST00000630858.2:c.1124T=	ENSP00000486514.1:p.Val375=
NM_001193416.2:c.1124T=	NP_001180345.1:p.Val375=
NM_001193417.2:c.1076T=	NP_001180346.1:p.Val359=
NM_001356.4:c.1124T=	NP_001347.3:p.Val375=
NR_126093.1:n.2069T=
XM_011543892.1:c.1124T=	XP_011542194.1:p.Val375=
NM_001363819.1:c.566T=	NP_001350748.1:p.Val189=
XM_011543892.2:c.1124T=	XP_011542194.1:p.Val375=
XM_017029313.1:c.566T=	XP_016884802.1:p.Val189=
NM_001193416.3:c.1124T=	NP_001180345.1:p.Val375=
NM_001193417.3:c.1076T=	NP_001180346.1:p.Val359=
NM_001356.5:c.1124T= MANE Select	NP_001347.3:p.Val375=