Canonical Allele Identifier: CA515972603

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205648T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346395T>A , CM000685.2:g.41346395T>A	GRCh38
NC_000023.10:g.41205648T>A , CM000685.1:g.41205648T>A	GRCh37
NC_000023.9:g.41090592T>A	NCBI36
NG_012830.1:g.17998T>A
NG_012830.2:g.17998T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1614T>A	ENSP00000496052.2:p.Ile538=
ENST00000399959.7:c.1479T>A	ENSP00000382840.3:p.Ile493=
ENST00000441189.4:c.1383T>A	ENSP00000414281.3:p.Ile461=
ENST00000457138.7:c.1434T>A	ENSP00000392494.2:p.Ile478=
ENST00000611968.2:c.76T>A
ENST00000616050.3:c.230T>A
ENST00000629496.3:c.1482T>A	ENSP00000487224.1:p.Ile494=
ENST00000642161.1:n.3681T>A
ENST00000642322.1:c.924T>A	ENSP00000496052.1:p.Ile308=
ENST00000642424.1:c.924T>A	ENSP00000496356.1:p.Ile308=
ENST00000642589.1:n.4804T>A
ENST00000642597.1:n.1656T>A
ENST00000642687.1:n.1515T>A
ENST00000642722.1:n.2315T>A
ENST00000642763.1:n.2373T>A
ENST00000642793.1:c.*931T>A	ENSP00000493976.1:n.*931T>A
ENST00000642801.1:n.1131T>A
ENST00000643820.1:n.758T>A
ENST00000643963.1:c.*764T>A	ENSP00000495264.1:n.*764T>A
ENST00000644073.1:c.1440T>A	ENSP00000493475.1:p.Ile480=
ENST00000644074.1:c.1479T>A	ENSP00000496663.1:p.Ile493=
ENST00000644109.1:c.1644T>A	ENSP00000494952.1:p.Ile548=
ENST00000644307.1:n.1652T>A
ENST00000644513.1:c.1482T>A	ENSP00000493819.1:p.Ile494=
ENST00000644677.1:c.1365T>A	ENSP00000496524.1:p.Ile455=
ENST00000644876.2:c.1482T>A MANE Select	ENSP00000494040.1:p.Ile494=
ENST00000644958.1:n.3143T>A
ENST00000645080.1:c.*2704T>A	ENSP00000494767.1:n.*2704T>A
ENST00000645120.1:n.2977T>A
ENST00000645338.1:n.1652T>A
ENST00000645380.1:n.2946T>A
ENST00000645561.1:n.2658T>A
ENST00000645574.1:n.4346T>A
ENST00000645589.1:c.1482T>A	ENSP00000494588.1:p.Ile494=
ENST00000646107.1:c.1365T>A	ENSP00000494518.1:p.Ile455=
ENST00000646122.1:c.1482T>A	ENSP00000496222.1:p.Ile494=
ENST00000646196.1:n.2451T>A
ENST00000646223.1:c.*1475T>A	ENSP00000496043.1:n.*1475T>A
ENST00000646319.1:c.1482T>A	ENSP00000495377.1:p.Ile494=
ENST00000646390.1:n.3770T>A
ENST00000646627.1:c.924T>A	ENSP00000493795.1:p.Ile308=
ENST00000646679.1:c.924T>A	ENSP00000494887.1:p.Ile308=
ENST00000646822.1:n.2544T>A
ENST00000646940.1:n.1656T>A
ENST00000647286.1:n.1580T>A
ENST00000647477.1:n.221T>A
ENST00000399959.6:c.1482T>A	ENSP00000382840.2:p.Ile494=
ENST00000441189.3:c.341-1245T>A	ENSP00000414281.2:n.341-1245T>A
ENST00000457138.6:c.1434T>A	ENSP00000392494.2:p.Ile478=
ENST00000478993.5:c.1482T>A	ENSP00000478443.1:p.Ile494=
ENST00000542215.5:n.1530T>A
ENST00000616050.2:c.35T>A
ENST00000625837.2:c.1482T>A	ENSP00000486306.1:p.Ile494=
ENST00000626301.2:c.1482T>A	ENSP00000486443.1:p.Ile494=
ENST00000629496.2:c.1482T>A	ENSP00000487224.1:p.Ile494=
ENST00000629785.2:c.1482T>A	ENSP00000486516.1:p.Ile494=
ENST00000630255.2:c.1482T>A	ENSP00000486720.1:p.Ile494=
ENST00000630370.2:c.1482T>A	ENSP00000487062.1:p.Ile494=
ENST00000630858.2:c.1482T>A	ENSP00000486514.1:p.Ile494=
NM_001193416.2:c.1482T>A	NP_001180345.1:p.Ile494=
NM_001193417.2:c.1434T>A	NP_001180346.1:p.Ile478=
NM_001356.4:c.1482T>A	NP_001347.3:p.Ile494=
NR_126093.1:n.2427T>A
XM_011543892.1:c.1482T>A	XP_011542194.1:p.Ile494=
NM_001363819.1:c.924T>A	NP_001350748.1:p.Ile308=
XM_011543892.2:c.1482T>A	XP_011542194.1:p.Ile494=
XM_017029313.1:c.924T>A	XP_016884802.1:p.Ile308=
NM_001193416.3:c.1482T>A	NP_001180345.1:p.Ile494=
NM_001193417.3:c.1434T>A	NP_001180346.1:p.Ile478=
NM_001356.5:c.1482T>A MANE Select	NP_001347.3:p.Ile494=