Canonical Allele Identifier: CA412775116

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205574A>T (hg19) ; chrX:g.41346321A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346321A>T , CM000685.2:g.41346321A>T	GRCh38
NC_000023.10:g.41205574A>T , CM000685.1:g.41205574A>T	GRCh37
NC_000023.9:g.41090518A>T	NCBI36
NG_012830.1:g.17924A>T
NG_012830.2:g.17924A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1540A>T	ENSP00000496052.2:p.Ser514Cys
ENST00000399959.7:c.1405A>T	ENSP00000382840.3:p.Ser469Cys
ENST00000441189.4:c.1309A>T	ENSP00000414281.3:p.Ser437Cys
ENST00000457138.7:c.1360A>T	ENSP00000392494.2:p.Ser454Cys
ENST00000611968.2:c.2A>T
ENST00000616050.3:c.156A>T
ENST00000629496.3:c.1408A>T	ENSP00000487224.1:p.Ser470Cys
ENST00000642161.1:n.3607A>T
ENST00000642322.1:c.850A>T	ENSP00000496052.1:p.Ser284Cys
ENST00000642424.1:c.850A>T	ENSP00000496356.1:p.Ser284Cys
ENST00000642589.1:n.4730A>T
ENST00000642597.1:n.1582A>T
ENST00000642687.1:n.1441A>T
ENST00000642722.1:n.2241A>T
ENST00000642763.1:n.2299A>T
ENST00000642793.1:c.*857A>T	ENSP00000493976.1:n.*857A>T
ENST00000642801.1:n.1057A>T
ENST00000643820.1:n.684A>T
ENST00000643963.1:c.*690A>T	ENSP00000495264.1:n.*690A>T
ENST00000644073.1:c.1366A>T	ENSP00000493475.1:p.Ser456Cys
ENST00000644074.1:c.1405A>T	ENSP00000496663.1:p.Ser469Cys
ENST00000644109.1:c.1570A>T	ENSP00000494952.1:p.Ser524Cys
ENST00000644307.1:n.1578A>T
ENST00000644513.1:c.1408A>T	ENSP00000493819.1:p.Ser470Cys
ENST00000644677.1:c.1291A>T	ENSP00000496524.1:p.Ser431Cys
ENST00000644876.2:c.1408A>T MANE Select	ENSP00000494040.1:p.Ser470Cys
ENST00000644958.1:n.3069A>T
ENST00000645080.1:c.*2630A>T	ENSP00000494767.1:n.*2630A>T
ENST00000645120.1:n.2903A>T
ENST00000645338.1:n.1578A>T
ENST00000645380.1:n.2872A>T
ENST00000645561.1:n.2584A>T
ENST00000645574.1:n.4272A>T
ENST00000645589.1:c.1408A>T	ENSP00000494588.1:p.Ser470Cys
ENST00000646107.1:c.1291A>T	ENSP00000494518.1:p.Ser431Cys
ENST00000646122.1:c.1408A>T	ENSP00000496222.1:p.Ser470Cys
ENST00000646196.1:n.2377A>T
ENST00000646223.1:c.*1401A>T	ENSP00000496043.1:n.*1401A>T
ENST00000646319.1:c.1408A>T	ENSP00000495377.1:p.Ser470Cys
ENST00000646390.1:n.3696A>T
ENST00000646627.1:c.850A>T	ENSP00000493795.1:p.Ser284Cys
ENST00000646679.1:c.850A>T	ENSP00000494887.1:p.Ser284Cys
ENST00000646822.1:n.2470A>T
ENST00000646940.1:n.1582A>T
ENST00000647286.1:n.1506A>T
ENST00000647477.1:n.147A>T
ENST00000399959.6:c.1408A>T	ENSP00000382840.2:p.Ser470Cys
ENST00000441189.3:c.341-1319A>T	ENSP00000414281.2:n.341-1319A>T
ENST00000457138.6:c.1360A>T	ENSP00000392494.2:p.Ser454Cys
ENST00000478993.5:c.1408A>T	ENSP00000478443.1:p.Ser470Cys
ENST00000542215.5:n.1456A>T
ENST00000625837.2:c.1408A>T	ENSP00000486306.1:p.Ser470Cys
ENST00000626301.2:c.1408A>T	ENSP00000486443.1:p.Ser470Cys
ENST00000629496.2:c.1408A>T	ENSP00000487224.1:p.Ser470Cys
ENST00000629785.2:c.1408A>T	ENSP00000486516.1:p.Ser470Cys
ENST00000630255.2:c.1408A>T	ENSP00000486720.1:p.Ser470Cys
ENST00000630370.2:c.1408A>T	ENSP00000487062.1:p.Ser470Cys
ENST00000630858.2:c.1408A>T	ENSP00000486514.1:p.Ser470Cys
NM_001193416.2:c.1408A>T	NP_001180345.1:p.Ser470Cys
NM_001193417.2:c.1360A>T	NP_001180346.1:p.Ser454Cys
NM_001356.4:c.1408A>T	NP_001347.3:p.Ser470Cys
NR_126093.1:n.2353A>T
XM_011543892.1:c.1408A>T	XP_011542194.1:p.Ser470Cys
NM_001363819.1:c.850A>T	NP_001350748.1:p.Ser284Cys
XM_011543892.2:c.1408A>T	XP_011542194.1:p.Ser470Cys
XM_017029313.1:c.850A>T	XP_016884802.1:p.Ser284Cys
NM_001193416.3:c.1408A>T	NP_001180345.1:p.Ser470Cys
NM_001193417.3:c.1360A>T	NP_001180346.1:p.Ser454Cys
NM_001356.5:c.1408A>T MANE Select	NP_001347.3:p.Ser470Cys