Canonical Allele Identifier: CA412771460

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204536C>T (hg19) ; chrX:g.41345283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345283C>T , CM000685.2:g.41345283C>T	GRCh38
NC_000023.10:g.41204536C>T , CM000685.1:g.41204536C>T	GRCh37
NC_000023.9:g.41089480C>T	NCBI36
NG_012830.1:g.16886C>T
NG_012830.2:g.16886C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1261C>T	ENSP00000496052.2:p.His421Tyr
ENST00000399959.7:c.1126C>T	ENSP00000382840.3:p.His376Tyr
ENST00000441189.4:c.1030C>T	ENSP00000414281.3:p.His344Tyr
ENST00000457138.7:c.1081C>T	ENSP00000392494.2:p.His361Tyr
ENST00000629496.3:c.1129C>T	ENSP00000487224.1:p.His377Tyr
ENST00000642161.1:n.3328C>T
ENST00000642322.1:c.571C>T	ENSP00000496052.1:p.His191Tyr
ENST00000642424.1:c.571C>T	ENSP00000496356.1:p.His191Tyr
ENST00000642589.1:n.4451C>T
ENST00000642597.1:n.1303C>T
ENST00000642687.1:n.1162C>T
ENST00000642722.1:n.1962C>T
ENST00000642763.1:n.2020C>T
ENST00000642793.1:c.*578C>T	ENSP00000493976.1:n.*578C>T
ENST00000642801.1:n.778C>T
ENST00000643820.1:n.405C>T
ENST00000643963.1:c.*411C>T	ENSP00000495264.1:n.*411C>T
ENST00000644073.1:c.1087C>T	ENSP00000493475.1:p.His363Tyr
ENST00000644074.1:c.1126C>T	ENSP00000496663.1:p.His376Tyr
ENST00000644109.1:c.1291C>T	ENSP00000494952.1:p.His431Tyr
ENST00000644307.1:n.1220C>T
ENST00000644513.1:c.1129C>T	ENSP00000493819.1:p.His377Tyr
ENST00000644677.1:c.1012C>T	ENSP00000496524.1:p.His338Tyr
ENST00000644876.2:c.1129C>T MANE Select	ENSP00000494040.1:p.His377Tyr
ENST00000644958.1:n.2790C>T
ENST00000645080.1:c.*2351C>T	ENSP00000494767.1:n.*2351C>T
ENST00000645120.1:n.2624C>T
ENST00000645338.1:n.1220C>T
ENST00000645380.1:n.2514C>T
ENST00000645561.1:n.2305C>T
ENST00000645574.1:n.3993C>T
ENST00000645589.1:c.1129C>T	ENSP00000494588.1:p.His377Tyr
ENST00000646093.1:n.313C>T
ENST00000646107.1:c.1012C>T	ENSP00000494518.1:p.His338Tyr
ENST00000646122.1:c.1129C>T	ENSP00000496222.1:p.His377Tyr
ENST00000646196.1:n.2098C>T
ENST00000646223.1:c.*1122C>T	ENSP00000496043.1:n.*1122C>T
ENST00000646319.1:c.1129C>T	ENSP00000495377.1:p.His377Tyr
ENST00000646390.1:n.3417C>T
ENST00000646627.1:c.571C>T	ENSP00000493795.1:p.His191Tyr
ENST00000646679.1:c.571C>T	ENSP00000494887.1:p.His191Tyr
ENST00000646822.1:n.2191C>T
ENST00000646940.1:n.1303C>T
ENST00000647286.1:n.1227C>T
ENST00000399959.6:c.1129C>T	ENSP00000382840.2:p.His377Tyr
ENST00000441189.3:c.341-2357C>T	ENSP00000414281.2:n.341-2357C>T
ENST00000457138.6:c.1081C>T	ENSP00000392494.2:p.His361Tyr
ENST00000478993.5:c.1129C>T	ENSP00000478443.1:p.His377Tyr
ENST00000542215.5:n.1177C>T
ENST00000625837.2:c.1129C>T	ENSP00000486306.1:p.His377Tyr
ENST00000626301.2:c.1129C>T	ENSP00000486443.1:p.His377Tyr
ENST00000629496.2:c.1129C>T	ENSP00000487224.1:p.His377Tyr
ENST00000629785.2:c.1129C>T	ENSP00000486516.1:p.His377Tyr
ENST00000630255.2:c.1129C>T	ENSP00000486720.1:p.His377Tyr
ENST00000630370.2:c.1129C>T	ENSP00000487062.1:p.His377Tyr
ENST00000630858.2:c.1129C>T	ENSP00000486514.1:p.His377Tyr
NM_001193416.2:c.1129C>T	NP_001180345.1:p.His377Tyr
NM_001193417.2:c.1081C>T	NP_001180346.1:p.His361Tyr
NM_001356.4:c.1129C>T	NP_001347.3:p.His377Tyr
NR_126093.1:n.2074C>T
XM_011543892.1:c.1129C>T	XP_011542194.1:p.His377Tyr
NM_001363819.1:c.571C>T	NP_001350748.1:p.His191Tyr
XM_011543892.2:c.1129C>T	XP_011542194.1:p.His377Tyr
XM_017029313.1:c.571C>T	XP_016884802.1:p.His191Tyr
NM_001193416.3:c.1129C>T	NP_001180345.1:p.His377Tyr
NM_001193417.3:c.1081C>T	NP_001180346.1:p.His361Tyr
NM_001356.5:c.1129C>T MANE Select	NP_001347.3:p.His377Tyr