Canonical Allele Identifier: CA412776788

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205837T>G (hg19) ; chrX:g.41346584T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346584T>G , CM000685.2:g.41346584T>G	GRCh38
NC_000023.10:g.41205837T>G , CM000685.1:g.41205837T>G	GRCh37
NC_000023.9:g.41090781T>G	NCBI36
NG_012830.1:g.18187T>G
NG_012830.2:g.18187T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1709T>G	ENSP00000496052.2:p.Val570Gly
ENST00000399959.7:c.1574T>G	ENSP00000382840.3:p.Val525Gly
ENST00000441189.4:c.1478T>G	ENSP00000414281.3:p.Val493Gly
ENST00000457138.7:c.1529T>G	ENSP00000392494.2:p.Val510Gly
ENST00000611968.2:c.171T>G
ENST00000616050.3:c.325T>G
ENST00000629496.3:c.1577T>G	ENSP00000487224.1:p.Val526Gly
ENST00000642161.1:n.3776T>G
ENST00000642322.1:c.1019T>G	ENSP00000496052.1:p.Val340Gly
ENST00000642424.1:c.1019T>G	ENSP00000496356.1:p.Val340Gly
ENST00000642589.1:n.4899T>G
ENST00000642597.1:n.1751T>G
ENST00000642687.1:n.1610T>G
ENST00000642722.1:n.2410T>G
ENST00000642763.1:n.2468T>G
ENST00000642793.1:c.*1026T>G	ENSP00000493976.1:n.*1026T>G
ENST00000642801.1:n.1226T>G
ENST00000643820.1:n.947T>G
ENST00000643963.1:c.*859T>G	ENSP00000495264.1:n.*859T>G
ENST00000644073.1:c.1535T>G	ENSP00000493475.1:p.Val512Gly
ENST00000644074.1:c.1574T>G	ENSP00000496663.1:p.Val525Gly
ENST00000644109.1:c.1739T>G	ENSP00000494952.1:p.Val580Gly
ENST00000644307.1:n.1747T>G
ENST00000644513.1:c.1577T>G	ENSP00000493819.1:p.Val526Gly
ENST00000644677.1:c.1460T>G	ENSP00000496524.1:p.Val487Gly
ENST00000644876.2:c.1577T>G MANE Select	ENSP00000494040.1:p.Val526Gly
ENST00000644958.1:n.3238T>G
ENST00000645080.1:c.*2799T>G	ENSP00000494767.1:n.*2799T>G
ENST00000645120.1:n.3072T>G
ENST00000645338.1:n.1747T>G
ENST00000645380.1:n.3041T>G
ENST00000645561.1:n.2753T>G
ENST00000645574.1:n.4441T>G
ENST00000645589.1:c.*76T>G	ENSP00000494588.1:n.*76T>G
ENST00000646107.1:c.1460T>G	ENSP00000494518.1:p.Val487Gly
ENST00000646122.1:c.1577T>G	ENSP00000496222.1:p.Val526Gly
ENST00000646196.1:n.2546T>G
ENST00000646223.1:c.*1570T>G	ENSP00000496043.1:n.*1570T>G
ENST00000646319.1:c.1577T>G	ENSP00000495377.1:p.Val526Gly
ENST00000646390.1:n.3865T>G
ENST00000646627.1:c.1019T>G	ENSP00000493795.1:p.Val340Gly
ENST00000646679.1:c.1019T>G	ENSP00000494887.1:p.Val340Gly
ENST00000646822.1:n.2639T>G
ENST00000646940.1:n.1751T>G
ENST00000647286.1:n.1675T>G
ENST00000647477.1:n.316T>G
ENST00000399959.6:c.1577T>G	ENSP00000382840.2:p.Val526Gly
ENST00000441189.3:c.341-1056T>G	ENSP00000414281.2:n.341-1056T>G
ENST00000457138.6:c.1529T>G	ENSP00000392494.2:p.Val510Gly
ENST00000478993.5:c.1577T>G	ENSP00000478443.1:p.Val526Gly
ENST00000611968.1:c.19T>G
ENST00000616050.2:c.130T>G
ENST00000625837.2:c.1577T>G	ENSP00000486306.1:p.Val526Gly
ENST00000626301.2:c.1577T>G	ENSP00000486443.1:p.Val526Gly
ENST00000629496.2:c.1577T>G	ENSP00000487224.1:p.Val526Gly
ENST00000629785.2:c.1577T>G	ENSP00000486516.1:p.Val526Gly
ENST00000630255.2:c.1577T>G	ENSP00000486720.1:p.Val526Gly
ENST00000630370.2:c.1577T>G	ENSP00000487062.1:p.Val526Gly
ENST00000630858.2:c.1577T>G	ENSP00000486514.1:p.Val526Gly
NM_001193416.2:c.1577T>G	NP_001180345.1:p.Val526Gly
NM_001193417.2:c.1529T>G	NP_001180346.1:p.Val510Gly
NM_001356.4:c.1577T>G	NP_001347.3:p.Val526Gly
NR_126093.1:n.2522T>G
XM_011543892.1:c.1577T>G	XP_011542194.1:p.Val526Gly
NM_001363819.1:c.1019T>G	NP_001350748.1:p.Val340Gly
XM_011543892.2:c.1577T>G	XP_011542194.1:p.Val526Gly
XM_017029313.1:c.1019T>G	XP_016884802.1:p.Val340Gly
NM_001193416.3:c.1577T>G	NP_001180345.1:p.Val526Gly
NM_001193417.3:c.1529T>G	NP_001180346.1:p.Val510Gly
NM_001356.5:c.1577T>G MANE Select	NP_001347.3:p.Val526Gly