Canonical Allele Identifier: CA412771432

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204522C>T (hg19) ; chrX:g.41345269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345269C>T , CM000685.2:g.41345269C>T	GRCh38
NC_000023.10:g.41204522C>T , CM000685.1:g.41204522C>T	GRCh37
NC_000023.9:g.41089466C>T	NCBI36
NG_012830.1:g.16872C>T
NG_012830.2:g.16872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1247C>T	ENSP00000496052.2:p.Pro416Leu
ENST00000399959.7:c.1112C>T	ENSP00000382840.3:p.Pro371Leu
ENST00000441189.4:c.1016C>T	ENSP00000414281.3:p.Pro339Leu
ENST00000457138.7:c.1067C>T	ENSP00000392494.2:p.Pro356Leu
ENST00000629496.3:c.1115C>T	ENSP00000487224.1:p.Pro372Leu
ENST00000642161.1:n.3314C>T
ENST00000642322.1:c.557C>T	ENSP00000496052.1:p.Pro186Leu
ENST00000642424.1:c.557C>T	ENSP00000496356.1:p.Pro186Leu
ENST00000642589.1:n.4437C>T
ENST00000642597.1:n.1289C>T
ENST00000642687.1:n.1148C>T
ENST00000642722.1:n.1948C>T
ENST00000642763.1:n.2006C>T
ENST00000642793.1:c.*564C>T	ENSP00000493976.1:n.*564C>T
ENST00000642801.1:n.764C>T
ENST00000643820.1:n.391C>T
ENST00000643963.1:c.*397C>T	ENSP00000495264.1:n.*397C>T
ENST00000644073.1:c.1073C>T	ENSP00000493475.1:p.Pro358Leu
ENST00000644074.1:c.1112C>T	ENSP00000496663.1:p.Pro371Leu
ENST00000644109.1:c.1277C>T	ENSP00000494952.1:p.Pro426Leu
ENST00000644307.1:n.1206C>T
ENST00000644513.1:c.1115C>T	ENSP00000493819.1:p.Pro372Leu
ENST00000644677.1:c.998C>T	ENSP00000496524.1:p.Pro333Leu
ENST00000644876.2:c.1115C>T MANE Select	ENSP00000494040.1:p.Pro372Leu
ENST00000644958.1:n.2776C>T
ENST00000645080.1:c.*2337C>T	ENSP00000494767.1:n.*2337C>T
ENST00000645120.1:n.2610C>T
ENST00000645338.1:n.1206C>T
ENST00000645380.1:n.2500C>T
ENST00000645561.1:n.2291C>T
ENST00000645574.1:n.3979C>T
ENST00000645589.1:c.1115C>T	ENSP00000494588.1:p.Pro372Leu
ENST00000646093.1:n.299C>T
ENST00000646107.1:c.998C>T	ENSP00000494518.1:p.Pro333Leu
ENST00000646122.1:c.1115C>T	ENSP00000496222.1:p.Pro372Leu
ENST00000646196.1:n.2084C>T
ENST00000646223.1:c.*1108C>T	ENSP00000496043.1:n.*1108C>T
ENST00000646319.1:c.1115C>T	ENSP00000495377.1:p.Pro372Leu
ENST00000646390.1:n.3403C>T
ENST00000646627.1:c.557C>T	ENSP00000493795.1:p.Pro186Leu
ENST00000646679.1:c.557C>T	ENSP00000494887.1:p.Pro186Leu
ENST00000646822.1:n.2177C>T
ENST00000646940.1:n.1289C>T
ENST00000647286.1:n.1213C>T
ENST00000399959.6:c.1115C>T	ENSP00000382840.2:p.Pro372Leu
ENST00000441189.3:c.341-2371C>T	ENSP00000414281.2:n.341-2371C>T
ENST00000457138.6:c.1067C>T	ENSP00000392494.2:p.Pro356Leu
ENST00000478993.5:c.1115C>T	ENSP00000478443.1:p.Pro372Leu
ENST00000542215.5:n.1163C>T
ENST00000625837.2:c.1115C>T	ENSP00000486306.1:p.Pro372Leu
ENST00000626301.2:c.1115C>T	ENSP00000486443.1:p.Pro372Leu
ENST00000629496.2:c.1115C>T	ENSP00000487224.1:p.Pro372Leu
ENST00000629785.2:c.1115C>T	ENSP00000486516.1:p.Pro372Leu
ENST00000630255.2:c.1115C>T	ENSP00000486720.1:p.Pro372Leu
ENST00000630370.2:c.1115C>T	ENSP00000487062.1:p.Pro372Leu
ENST00000630858.2:c.1115C>T	ENSP00000486514.1:p.Pro372Leu
NM_001193416.2:c.1115C>T	NP_001180345.1:p.Pro372Leu
NM_001193417.2:c.1067C>T	NP_001180346.1:p.Pro356Leu
NM_001356.4:c.1115C>T	NP_001347.3:p.Pro372Leu
NR_126093.1:n.2060C>T
XM_011543892.1:c.1115C>T	XP_011542194.1:p.Pro372Leu
NM_001363819.1:c.557C>T	NP_001350748.1:p.Pro186Leu
XM_011543892.2:c.1115C>T	XP_011542194.1:p.Pro372Leu
XM_017029313.1:c.557C>T	XP_016884802.1:p.Pro186Leu
NM_001193416.3:c.1115C>T	NP_001180345.1:p.Pro372Leu
NM_001193417.3:c.1067C>T	NP_001180346.1:p.Pro356Leu
NM_001356.5:c.1115C>T MANE Select	NP_001347.3:p.Pro372Leu