Canonical Allele Identifier: CA412775641

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205622C>T (hg19) ; chrX:g.41346369C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346369C>T , CM000685.2:g.41346369C>T	GRCh38
NC_000023.10:g.41205622C>T , CM000685.1:g.41205622C>T	GRCh37
NC_000023.9:g.41090566C>T	NCBI36
NG_012830.1:g.17972C>T
NG_012830.2:g.17972C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1588C>T	ENSP00000496052.2:p.Gln530Ter
ENST00000399959.7:c.1453C>T	ENSP00000382840.3:p.Gln485Ter
ENST00000441189.4:c.1357C>T	ENSP00000414281.3:p.Gln453Ter
ENST00000457138.7:c.1408C>T	ENSP00000392494.2:p.Gln470Ter
ENST00000611968.2:c.50C>T
ENST00000616050.3:c.204C>T
ENST00000629496.3:c.1456C>T	ENSP00000487224.1:p.Gln486Ter
ENST00000642161.1:n.3655C>T
ENST00000642322.1:c.898C>T	ENSP00000496052.1:p.Gln300Ter
ENST00000642424.1:c.898C>T	ENSP00000496356.1:p.Gln300Ter
ENST00000642589.1:n.4778C>T
ENST00000642597.1:n.1630C>T
ENST00000642687.1:n.1489C>T
ENST00000642722.1:n.2289C>T
ENST00000642763.1:n.2347C>T
ENST00000642793.1:c.*905C>T	ENSP00000493976.1:n.*905C>T
ENST00000642801.1:n.1105C>T
ENST00000643820.1:n.732C>T
ENST00000643963.1:c.*738C>T	ENSP00000495264.1:n.*738C>T
ENST00000644073.1:c.1414C>T	ENSP00000493475.1:p.Gln472Ter
ENST00000644074.1:c.1453C>T	ENSP00000496663.1:p.Gln485Ter
ENST00000644109.1:c.1618C>T	ENSP00000494952.1:p.Gln540Ter
ENST00000644307.1:n.1626C>T
ENST00000644513.1:c.1456C>T	ENSP00000493819.1:p.Gln486Ter
ENST00000644677.1:c.1339C>T	ENSP00000496524.1:p.Gln447Ter
ENST00000644876.2:c.1456C>T MANE Select	ENSP00000494040.1:p.Gln486Ter
ENST00000644958.1:n.3117C>T
ENST00000645080.1:c.*2678C>T	ENSP00000494767.1:n.*2678C>T
ENST00000645120.1:n.2951C>T
ENST00000645338.1:n.1626C>T
ENST00000645380.1:n.2920C>T
ENST00000645561.1:n.2632C>T
ENST00000645574.1:n.4320C>T
ENST00000645589.1:c.1456C>T	ENSP00000494588.1:p.Gln486Ter
ENST00000646107.1:c.1339C>T	ENSP00000494518.1:p.Gln447Ter
ENST00000646122.1:c.1456C>T	ENSP00000496222.1:p.Gln486Ter
ENST00000646196.1:n.2425C>T
ENST00000646223.1:c.*1449C>T	ENSP00000496043.1:n.*1449C>T
ENST00000646319.1:c.1456C>T	ENSP00000495377.1:p.Gln486Ter
ENST00000646390.1:n.3744C>T
ENST00000646627.1:c.898C>T	ENSP00000493795.1:p.Gln300Ter
ENST00000646679.1:c.898C>T	ENSP00000494887.1:p.Gln300Ter
ENST00000646822.1:n.2518C>T
ENST00000646940.1:n.1630C>T
ENST00000647286.1:n.1554C>T
ENST00000647477.1:n.195C>T
ENST00000399959.6:c.1456C>T	ENSP00000382840.2:p.Gln486Ter
ENST00000441189.3:c.341-1271C>T	ENSP00000414281.2:n.341-1271C>T
ENST00000457138.6:c.1408C>T	ENSP00000392494.2:p.Gln470Ter
ENST00000478993.5:c.1456C>T	ENSP00000478443.1:p.Gln486Ter
ENST00000542215.5:n.1504C>T
ENST00000616050.2:c.9C>T
ENST00000625837.2:c.1456C>T	ENSP00000486306.1:p.Gln486Ter
ENST00000626301.2:c.1456C>T	ENSP00000486443.1:p.Gln486Ter
ENST00000629496.2:c.1456C>T	ENSP00000487224.1:p.Gln486Ter
ENST00000629785.2:c.1456C>T	ENSP00000486516.1:p.Gln486Ter
ENST00000630255.2:c.1456C>T	ENSP00000486720.1:p.Gln486Ter
ENST00000630370.2:c.1456C>T	ENSP00000487062.1:p.Gln486Ter
ENST00000630858.2:c.1456C>T	ENSP00000486514.1:p.Gln486Ter
NM_001193416.2:c.1456C>T	NP_001180345.1:p.Gln486Ter
NM_001193417.2:c.1408C>T	NP_001180346.1:p.Gln470Ter
NM_001356.4:c.1456C>T	NP_001347.3:p.Gln486Ter
NR_126093.1:n.2401C>T
XM_011543892.1:c.1456C>T	XP_011542194.1:p.Gln486Ter
NM_001363819.1:c.898C>T	NP_001350748.1:p.Gln300Ter
XM_011543892.2:c.1456C>T	XP_011542194.1:p.Gln486Ter
XM_017029313.1:c.898C>T	XP_016884802.1:p.Gln300Ter
NM_001193416.3:c.1456C>T	NP_001180345.1:p.Gln486Ter
NM_001193417.3:c.1408C>T	NP_001180346.1:p.Gln470Ter
NM_001356.5:c.1456C>T MANE Select	NP_001347.3:p.Gln486Ter