Canonical Allele Identifier: CA412771144

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41203627G>T (hg19) ; chrX:g.41344374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344374G>T , CM000685.2:g.41344374G>T	GRCh38
NC_000023.10:g.41203627G>T , CM000685.1:g.41203627G>T	GRCh37
NC_000023.9:g.41088571G>T	NCBI36
NG_012830.1:g.15977G>T
NG_012830.2:g.15977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1132G>T	ENSP00000496052.2:p.Gly378Ter
ENST00000399959.7:c.997G>T	ENSP00000382840.3:p.Gly333Ter
ENST00000441189.4:c.901G>T	ENSP00000414281.3:p.Gly301Ter
ENST00000457138.7:c.952G>T	ENSP00000392494.2:p.Gly318Ter
ENST00000629496.3:c.1000G>T	ENSP00000487224.1:p.Gly334Ter
ENST00000631641.2:n.1043G>T
ENST00000642161.1:n.3199G>T
ENST00000642322.1:c.442G>T	ENSP00000496052.1:p.Gly148Ter
ENST00000642424.1:c.442G>T	ENSP00000496356.1:p.Gly148Ter
ENST00000642589.1:n.4322G>T
ENST00000642597.1:n.1174G>T
ENST00000642687.1:n.1033G>T
ENST00000642722.1:n.1833G>T
ENST00000642763.1:n.1891G>T
ENST00000642793.1:c.*449G>T	ENSP00000493976.1:n.*449G>T
ENST00000642801.1:n.649G>T
ENST00000643820.1:n.276G>T
ENST00000643963.1:c.*282G>T	ENSP00000495264.1:n.*282G>T
ENST00000644073.1:c.958G>T	ENSP00000493475.1:p.Gly320Ter
ENST00000644074.1:c.997G>T	ENSP00000496663.1:p.Gly333Ter
ENST00000644109.1:c.997G>T	ENSP00000494952.1:p.Gly333Ter
ENST00000644307.1:n.1091G>T
ENST00000644513.1:c.1000G>T	ENSP00000493819.1:p.Gly334Ter
ENST00000644677.1:c.883G>T	ENSP00000496524.1:p.Gly295Ter
ENST00000644876.2:c.1000G>T MANE Select	ENSP00000494040.1:p.Gly334Ter
ENST00000644958.1:n.2661G>T
ENST00000645080.1:c.*2222G>T	ENSP00000494767.1:n.*2222G>T
ENST00000645120.1:n.2495G>T
ENST00000645338.1:n.1091G>T
ENST00000645380.1:n.2385G>T
ENST00000645561.1:n.2176G>T
ENST00000645574.1:n.3864G>T
ENST00000645589.1:c.1000G>T	ENSP00000494588.1:p.Gly334Ter
ENST00000646093.1:n.184G>T
ENST00000646107.1:c.883G>T	ENSP00000494518.1:p.Gly295Ter
ENST00000646122.1:c.1000G>T	ENSP00000496222.1:p.Gly334Ter
ENST00000646196.1:n.1969G>T
ENST00000646223.1:c.*993G>T	ENSP00000496043.1:n.*993G>T
ENST00000646319.1:c.1000G>T	ENSP00000495377.1:p.Gly334Ter
ENST00000646390.1:n.3288G>T
ENST00000646627.1:c.442G>T	ENSP00000493795.1:p.Gly148Ter
ENST00000646679.1:c.442G>T	ENSP00000494887.1:p.Gly148Ter
ENST00000646822.1:n.2062G>T
ENST00000646940.1:n.1174G>T
ENST00000647286.1:n.1098G>T
ENST00000399959.6:c.1000G>T	ENSP00000382840.2:p.Gly334Ter
ENST00000441189.3:c.340+1824G>T	ENSP00000414281.2:n.340+1824G>T
ENST00000457138.6:c.952G>T	ENSP00000392494.2:p.Gly318Ter
ENST00000478993.5:c.1000G>T	ENSP00000478443.1:p.Gly334Ter
ENST00000542215.5:n.1048G>T
ENST00000625837.2:c.1000G>T	ENSP00000486306.1:p.Gly334Ter
ENST00000626301.2:c.1000G>T	ENSP00000486443.1:p.Gly334Ter
ENST00000629496.2:c.1000G>T	ENSP00000487224.1:p.Gly334Ter
ENST00000629785.2:c.1000G>T	ENSP00000486516.1:p.Gly334Ter
ENST00000630255.2:c.1000G>T	ENSP00000486720.1:p.Gly334Ter
ENST00000630370.2:c.1000G>T	ENSP00000487062.1:p.Gly334Ter
ENST00000630858.2:c.1000G>T	ENSP00000486514.1:p.Gly334Ter
NM_001193416.2:c.1000G>T	NP_001180345.1:p.Gly334Ter
NM_001193417.2:c.952G>T	NP_001180346.1:p.Gly318Ter
NM_001356.4:c.1000G>T	NP_001347.3:p.Gly334Ter
NR_126093.1:n.1945G>T
XM_011543892.1:c.1000G>T	XP_011542194.1:p.Gly334Ter
NM_001363819.1:c.442G>T	NP_001350748.1:p.Gly148Ter
XM_011543892.2:c.1000G>T	XP_011542194.1:p.Gly334Ter
XM_017029313.1:c.442G>T	XP_016884802.1:p.Gly148Ter
NM_001193416.3:c.1000G>T	NP_001180345.1:p.Gly334Ter
NM_001193417.3:c.952G>T	NP_001180346.1:p.Gly318Ter
NM_001356.5:c.1000G>T MANE Select	NP_001347.3:p.Gly334Ter