Canonical Allele Identifier: CA2579588693

Gene: DDX3X

Linked Data

• gnomAD v4: X-41344150-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344150T>C , CM000685.2:g.41344150T>C	GRCh38
NC_000023.10:g.41203403T>C , CM000685.1:g.41203403T>C	GRCh37
NC_000023.9:g.41088347T>C	NCBI36
NG_012830.1:g.15753T>C
NG_012830.2:g.15753T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.996+22T>C	ENSP00000496052.2:n.996+22T>C
ENST00000399959.7:c.861+22T>C	ENSP00000382840.3:n.861+22T>C
ENST00000441189.4:c.766-89T>C	ENSP00000414281.3:n.766-89T>C
ENST00000457138.7:c.816+22T>C	ENSP00000392494.2:n.816+22T>C
ENST00000629496.3:c.864+22T>C	ENSP00000487224.1:n.864+22T>C
ENST00000631641.2:n.907+22T>C
ENST00000642161.1:n.3063+22T>C
ENST00000642322.1:c.306+22T>C	ENSP00000496052.1:n.306+22T>C
ENST00000642424.1:c.306+22T>C	ENSP00000496356.1:n.306+22T>C
ENST00000642589.1:n.4186+22T>C
ENST00000642597.1:n.1038+22T>C
ENST00000642687.1:n.897+22T>C
ENST00000642722.1:n.1697+22T>C
ENST00000642763.1:n.1755+22T>C
ENST00000642793.1:c.*313+22T>C	ENSP00000493976.1:n.*313+22T>C
ENST00000642801.1:n.513+22T>C
ENST00000643820.1:n.140+22T>C
ENST00000643963.1:c.*146+22T>C	ENSP00000495264.1:n.*146+22T>C
ENST00000644073.1:c.822+22T>C	ENSP00000493475.1:n.822+22T>C
ENST00000644074.1:c.861+22T>C	ENSP00000496663.1:n.861+22T>C
ENST00000644109.1:c.861+22T>C	ENSP00000494952.1:n.861+22T>C
ENST00000644307.1:n.955+22T>C
ENST00000644513.1:c.864+22T>C	ENSP00000493819.1:n.864+22T>C
ENST00000644677.1:c.747+22T>C	ENSP00000496524.1:n.747+22T>C
ENST00000644876.2:c.864+22T>C MANE Select	ENSP00000494040.1:n.864+22T>C
ENST00000644958.1:n.2525+22T>C
ENST00000645080.1:c.*2086+22T>C	ENSP00000494767.1:n.*2086+22T>C
ENST00000645120.1:n.2359+22T>C
ENST00000645338.1:n.955+22T>C
ENST00000645380.1:n.2249+22T>C
ENST00000645561.1:n.2040+22T>C
ENST00000645574.1:n.3728+22T>C
ENST00000645589.1:c.864+22T>C	ENSP00000494588.1:n.864+22T>C
ENST00000646107.1:c.747+22T>C	ENSP00000494518.1:n.747+22T>C
ENST00000646122.1:c.864+22T>C	ENSP00000496222.1:n.864+22T>C
ENST00000646196.1:n.1833+22T>C
ENST00000646223.1:c.*857+22T>C	ENSP00000496043.1:n.*857+22T>C
ENST00000646319.1:c.864+22T>C	ENSP00000495377.1:n.864+22T>C
ENST00000646390.1:n.3152+22T>C
ENST00000646627.1:c.306+22T>C	ENSP00000493795.1:n.306+22T>C
ENST00000646679.1:c.306+22T>C	ENSP00000494887.1:n.306+22T>C
ENST00000646822.1:n.1926+22T>C
ENST00000646940.1:n.1038+22T>C
ENST00000647286.1:n.962+22T>C
ENST00000399959.6:c.864+22T>C	ENSP00000382840.2:n.864+22T>C
ENST00000441189.3:c.340+1600T>C	ENSP00000414281.2:n.340+1600T>C
ENST00000457138.6:c.816+22T>C	ENSP00000392494.2:n.816+22T>C
ENST00000478993.5:c.864+22T>C	ENSP00000478443.1:n.864+22T>C
ENST00000542215.5:n.912+22T>C
ENST00000625837.2:c.864+22T>C	ENSP00000486306.1:n.864+22T>C
ENST00000626301.2:c.864+22T>C	ENSP00000486443.1:n.864+22T>C
ENST00000629496.2:c.864+22T>C	ENSP00000487224.1:n.864+22T>C
ENST00000629785.2:c.864+22T>C	ENSP00000486516.1:n.864+22T>C
ENST00000630255.2:c.864+22T>C	ENSP00000486720.1:n.864+22T>C
ENST00000630370.2:c.864+22T>C	ENSP00000487062.1:n.864+22T>C
ENST00000630858.2:c.864+22T>C	ENSP00000486514.1:n.864+22T>C
NM_001193416.2:c.864+22T>C	NP_001180345.1:n.864+22T>C
NM_001193417.2:c.816+22T>C	NP_001180346.1:n.816+22T>C
NM_001356.4:c.864+22T>C	NP_001347.3:n.864+22T>C
NR_126093.1:n.1809+22T>C
XM_011543892.1:c.864+22T>C	XP_011542194.1:n.864+22T>C
NM_001363819.1:c.306+22T>C	NP_001350748.1:n.306+22T>C
XM_011543892.2:c.864+22T>C	XP_011542194.1:n.864+22T>C
XM_017029313.1:c.306+22T>C	XP_016884802.1:n.306+22T>C
NM_001193416.3:c.864+22T>C	NP_001180345.1:n.864+22T>C
NM_001193417.3:c.816+22T>C	NP_001180346.1:n.816+22T>C
NM_001356.5:c.864+22T>C MANE Select	NP_001347.3:n.864+22T>C