Canonical Allele Identifier: CA412770542

Gene: DDX3X

Linked Data

• dbSNP Id: rs1255183431
• gnomAD v2: X-41203491-G-T
• gnomAD v4: X-41344238-G-T
• MyVariant Identifiers: chrX:g.41203491G>T (hg19) ; chrX:g.41344238G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41344238G>T , CM000685.2:g.41344238G>T	GRCh38
NC_000023.10:g.41203491G>T , CM000685.1:g.41203491G>T	GRCh37
NC_000023.9:g.41088435G>T	NCBI36
NG_012830.1:g.15841G>T
NG_012830.2:g.15841G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.997-1G>T	ENSP00000496052.2:n.997-1G>T
ENST00000399959.7:c.862-1G>T	ENSP00000382840.3:n.862-1G>T
ENST00000441189.4:c.766-1G>T	ENSP00000414281.3:n.766-1G>T
ENST00000457138.7:c.817-1G>T	ENSP00000392494.2:n.817-1G>T
ENST00000629496.3:c.865-1G>T	ENSP00000487224.1:n.865-1G>T
ENST00000631641.2:n.908-1G>T
ENST00000642161.1:n.3064-1G>T
ENST00000642322.1:c.307-1G>T	ENSP00000496052.1:n.307-1G>T
ENST00000642424.1:c.307-1G>T	ENSP00000496356.1:n.307-1G>T
ENST00000642589.1:n.4187-1G>T
ENST00000642597.1:n.1039-1G>T
ENST00000642687.1:n.898-1G>T
ENST00000642722.1:n.1698-1G>T
ENST00000642763.1:n.1756-1G>T
ENST00000642793.1:c.*314-1G>T	ENSP00000493976.1:n.*314-1G>T
ENST00000642801.1:n.514-1G>T
ENST00000643820.1:n.141-1G>T
ENST00000643963.1:c.*147-1G>T	ENSP00000495264.1:n.*147-1G>T
ENST00000644073.1:c.823-1G>T	ENSP00000493475.1:n.823-1G>T
ENST00000644074.1:c.862-1G>T	ENSP00000496663.1:n.862-1G>T
ENST00000644109.1:c.862-1G>T	ENSP00000494952.1:n.862-1G>T
ENST00000644307.1:n.956-1G>T
ENST00000644513.1:c.865-1G>T	ENSP00000493819.1:n.865-1G>T
ENST00000644677.1:c.748-1G>T	ENSP00000496524.1:n.748-1G>T
ENST00000644876.2:c.865-1G>T MANE Select	ENSP00000494040.1:n.865-1G>T
ENST00000644958.1:n.2526-1G>T
ENST00000645080.1:c.*2087-1G>T	ENSP00000494767.1:n.*2087-1G>T
ENST00000645120.1:n.2360-1G>T
ENST00000645338.1:n.956-1G>T
ENST00000645380.1:n.2250-1G>T
ENST00000645561.1:n.2041-1G>T
ENST00000645574.1:n.3729-1G>T
ENST00000645589.1:c.865-1G>T	ENSP00000494588.1:n.865-1G>T
ENST00000646093.1:n.48G>T
ENST00000646107.1:c.748-1G>T	ENSP00000494518.1:n.748-1G>T
ENST00000646122.1:c.865-1G>T	ENSP00000496222.1:n.865-1G>T
ENST00000646196.1:n.1834-1G>T
ENST00000646223.1:c.*858-1G>T	ENSP00000496043.1:n.*858-1G>T
ENST00000646319.1:c.865-1G>T	ENSP00000495377.1:n.865-1G>T
ENST00000646390.1:n.3153-1G>T
ENST00000646627.1:c.307-1G>T	ENSP00000493795.1:n.307-1G>T
ENST00000646679.1:c.307-1G>T	ENSP00000494887.1:n.307-1G>T
ENST00000646822.1:n.1927-1G>T
ENST00000646940.1:n.1039-1G>T
ENST00000647286.1:n.963-1G>T
ENST00000399959.6:c.865-1G>T	ENSP00000382840.2:n.865-1G>T
ENST00000441189.3:c.340+1688G>T	ENSP00000414281.2:n.340+1688G>T
ENST00000457138.6:c.817-1G>T	ENSP00000392494.2:n.817-1G>T
ENST00000478993.5:c.865-1G>T	ENSP00000478443.1:n.865-1G>T
ENST00000542215.5:n.913-1G>T
ENST00000625837.2:c.865-1G>T	ENSP00000486306.1:n.865-1G>T
ENST00000626301.2:c.865-1G>T	ENSP00000486443.1:n.865-1G>T
ENST00000629496.2:c.865-1G>T	ENSP00000487224.1:n.865-1G>T
ENST00000629785.2:c.865-1G>T	ENSP00000486516.1:n.865-1G>T
ENST00000630255.2:c.865-1G>T	ENSP00000486720.1:n.865-1G>T
ENST00000630370.2:c.865-1G>T	ENSP00000487062.1:n.865-1G>T
ENST00000630858.2:c.865-1G>T	ENSP00000486514.1:n.865-1G>T
NM_001193416.2:c.865-1G>T	NP_001180345.1:n.865-1G>T
NM_001193417.2:c.817-1G>T	NP_001180346.1:n.817-1G>T
NM_001356.4:c.865-1G>T	NP_001347.3:n.865-1G>T
NR_126093.1:n.1810-1G>T
XM_011543892.1:c.865-1G>T	XP_011542194.1:n.865-1G>T
NM_001363819.1:c.307-1G>T	NP_001350748.1:n.307-1G>T
XM_011543892.2:c.865-1G>T	XP_011542194.1:n.865-1G>T
XM_017029313.1:c.307-1G>T	XP_016884802.1:n.307-1G>T
NM_001193416.3:c.865-1G>T	NP_001180345.1:n.865-1G>T
NM_001193417.3:c.817-1G>T	NP_001180346.1:n.817-1G>T
NM_001356.5:c.865-1G>T MANE Select	NP_001347.3:n.865-1G>T