Canonical Allele Identifier: CA2425881033

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345238C= , CM000685.2:g.41345238C=	GRCh38
NC_000023.10:g.41204491C= , CM000685.1:g.41204491C=	GRCh37
NC_000023.9:g.41089435C=	NCBI36
NG_012830.1:g.16841C=
NG_012830.2:g.16841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1216C=	ENSP00000496052.2:p.Arg406=
ENST00000399959.7:c.1081C=	ENSP00000382840.3:p.Arg361=
ENST00000441189.4:c.985C=	ENSP00000414281.3:p.Arg329=
ENST00000457138.7:c.1036C=	ENSP00000392494.2:p.Arg346=
ENST00000629496.3:c.1084C=	ENSP00000487224.1:p.Arg362=
ENST00000642161.1:n.3283C=
ENST00000642322.1:c.526C=	ENSP00000496052.1:p.Arg176=
ENST00000642424.1:c.526C=	ENSP00000496356.1:p.Arg176=
ENST00000642589.1:n.4406C=
ENST00000642597.1:n.1258C=
ENST00000642687.1:n.1117C=
ENST00000642722.1:n.1917C=
ENST00000642763.1:n.1975C=
ENST00000642793.1:c.*533C=	ENSP00000493976.1:n.*533C=
ENST00000642801.1:n.733C=
ENST00000643820.1:n.360C=
ENST00000643963.1:c.*366C=	ENSP00000495264.1:n.*366C=
ENST00000644073.1:c.1042C=	ENSP00000493475.1:p.Arg348=
ENST00000644074.1:c.1081C=	ENSP00000496663.1:p.Arg361=
ENST00000644109.1:c.1246C=	ENSP00000494952.1:p.Arg416=
ENST00000644307.1:n.1175C=
ENST00000644513.1:c.1084C=	ENSP00000493819.1:p.Arg362=
ENST00000644677.1:c.967C=	ENSP00000496524.1:p.Arg323=
ENST00000644876.2:c.1084C= MANE Select	ENSP00000494040.1:p.Arg362=
ENST00000644958.1:n.2745C=
ENST00000645080.1:c.*2306C=	ENSP00000494767.1:n.*2306C=
ENST00000645120.1:n.2579C=
ENST00000645338.1:n.1175C=
ENST00000645380.1:n.2469C=
ENST00000645561.1:n.2260C=
ENST00000645574.1:n.3948C=
ENST00000645589.1:c.1084C=	ENSP00000494588.1:p.Arg362=
ENST00000646093.1:n.268C=
ENST00000646107.1:c.967C=	ENSP00000494518.1:p.Arg323=
ENST00000646122.1:c.1084C=	ENSP00000496222.1:p.Arg362=
ENST00000646196.1:n.2053C=
ENST00000646223.1:c.*1077C=	ENSP00000496043.1:n.*1077C=
ENST00000646319.1:c.1084C=	ENSP00000495377.1:p.Arg362=
ENST00000646390.1:n.3372C=
ENST00000646627.1:c.526C=	ENSP00000493795.1:p.Arg176=
ENST00000646679.1:c.526C=	ENSP00000494887.1:p.Arg176=
ENST00000646822.1:n.2146C=
ENST00000646940.1:n.1258C=
ENST00000647286.1:n.1182C=
ENST00000399959.6:c.1084C=	ENSP00000382840.2:p.Arg362=
ENST00000441189.3:c.341-2402C=	ENSP00000414281.2:n.341-2402C=
ENST00000457138.6:c.1036C=	ENSP00000392494.2:p.Arg346=
ENST00000478993.5:c.1084C=	ENSP00000478443.1:p.Arg362=
ENST00000542215.5:n.1132C=
ENST00000625837.2:c.1084C=	ENSP00000486306.1:p.Arg362=
ENST00000626301.2:c.1084C=	ENSP00000486443.1:p.Arg362=
ENST00000629496.2:c.1084C=	ENSP00000487224.1:p.Arg362=
ENST00000629785.2:c.1084C=	ENSP00000486516.1:p.Arg362=
ENST00000630255.2:c.1084C=	ENSP00000486720.1:p.Arg362=
ENST00000630370.2:c.1084C=	ENSP00000487062.1:p.Arg362=
ENST00000630858.2:c.1084C=	ENSP00000486514.1:p.Arg362=
NM_001193416.2:c.1084C=	NP_001180345.1:p.Arg362=
NM_001193417.2:c.1036C=	NP_001180346.1:p.Arg346=
NM_001356.4:c.1084C=	NP_001347.3:p.Arg362=
NR_126093.1:n.2029C=
XM_011543892.1:c.1084C=	XP_011542194.1:p.Arg362=
NM_001363819.1:c.526C=	NP_001350748.1:p.Arg176=
XM_011543892.2:c.1084C=	XP_011542194.1:p.Arg362=
XM_017029313.1:c.526C=	XP_016884802.1:p.Arg176=
NM_001193416.3:c.1084C=	NP_001180345.1:p.Arg362=
NM_001193417.3:c.1036C=	NP_001180346.1:p.Arg346=
NM_001356.5:c.1084C= MANE Select	NP_001347.3:p.Arg362=