Canonical Allele Identifier: CA412771244

Gene: DDX3X

Linked Data

• ClinVar Variation Id: 2727763
• ClinVar RCV Id: RCV003557279
• MyVariant Identifiers: chrX:g.41204444T>C (hg19) ; chrX:g.41345191T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345191T>C , CM000685.2:g.41345191T>C	GRCh38
NC_000023.10:g.41204444T>C , CM000685.1:g.41204444T>C	GRCh37
NC_000023.9:g.41089388T>C	NCBI36
NG_012830.1:g.16794T>C
NG_012830.2:g.16794T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1169T>C	ENSP00000496052.2:p.Leu390Ser
ENST00000399959.7:c.1034T>C	ENSP00000382840.3:p.Leu345Ser
ENST00000441189.4:c.938T>C	ENSP00000414281.3:p.Leu313Ser
ENST00000457138.7:c.989T>C	ENSP00000392494.2:p.Leu330Ser
ENST00000629496.3:c.1037T>C	ENSP00000487224.1:p.Leu346Ser
ENST00000642161.1:n.3236T>C
ENST00000642322.1:c.479T>C	ENSP00000496052.1:p.Leu160Ser
ENST00000642424.1:c.479T>C	ENSP00000496356.1:p.Leu160Ser
ENST00000642589.1:n.4359T>C
ENST00000642597.1:n.1211T>C
ENST00000642687.1:n.1070T>C
ENST00000642722.1:n.1870T>C
ENST00000642763.1:n.1928T>C
ENST00000642793.1:c.*486T>C	ENSP00000493976.1:n.*486T>C
ENST00000642801.1:n.686T>C
ENST00000643820.1:n.313T>C
ENST00000643963.1:c.*319T>C	ENSP00000495264.1:n.*319T>C
ENST00000644073.1:c.995T>C	ENSP00000493475.1:p.Leu332Ser
ENST00000644074.1:c.1034T>C	ENSP00000496663.1:p.Leu345Ser
ENST00000644109.1:c.1199T>C	ENSP00000494952.1:p.Leu400Ser
ENST00000644307.1:n.1128T>C
ENST00000644513.1:c.1037T>C	ENSP00000493819.1:p.Leu346Ser
ENST00000644677.1:c.920T>C	ENSP00000496524.1:p.Leu307Ser
ENST00000644876.2:c.1037T>C MANE Select	ENSP00000494040.1:p.Leu346Ser
ENST00000644958.1:n.2698T>C
ENST00000645080.1:c.*2259T>C	ENSP00000494767.1:n.*2259T>C
ENST00000645120.1:n.2532T>C
ENST00000645338.1:n.1128T>C
ENST00000645380.1:n.2422T>C
ENST00000645561.1:n.2213T>C
ENST00000645574.1:n.3901T>C
ENST00000645589.1:c.1037T>C	ENSP00000494588.1:p.Leu346Ser
ENST00000646093.1:n.221T>C
ENST00000646107.1:c.920T>C	ENSP00000494518.1:p.Leu307Ser
ENST00000646122.1:c.1037T>C	ENSP00000496222.1:p.Leu346Ser
ENST00000646196.1:n.2006T>C
ENST00000646223.1:c.*1030T>C	ENSP00000496043.1:n.*1030T>C
ENST00000646319.1:c.1037T>C	ENSP00000495377.1:p.Leu346Ser
ENST00000646390.1:n.3325T>C
ENST00000646627.1:c.479T>C	ENSP00000493795.1:p.Leu160Ser
ENST00000646679.1:c.479T>C	ENSP00000494887.1:p.Leu160Ser
ENST00000646822.1:n.2099T>C
ENST00000646940.1:n.1211T>C
ENST00000647286.1:n.1135T>C
ENST00000399959.6:c.1037T>C	ENSP00000382840.2:p.Leu346Ser
ENST00000441189.3:c.341-2449T>C	ENSP00000414281.2:n.341-2449T>C
ENST00000457138.6:c.989T>C	ENSP00000392494.2:p.Leu330Ser
ENST00000478993.5:c.1037T>C	ENSP00000478443.1:p.Leu346Ser
ENST00000542215.5:n.1085T>C
ENST00000625837.2:c.1037T>C	ENSP00000486306.1:p.Leu346Ser
ENST00000626301.2:c.1037T>C	ENSP00000486443.1:p.Leu346Ser
ENST00000629496.2:c.1037T>C	ENSP00000487224.1:p.Leu346Ser
ENST00000629785.2:c.1037T>C	ENSP00000486516.1:p.Leu346Ser
ENST00000630255.2:c.1037T>C	ENSP00000486720.1:p.Leu346Ser
ENST00000630370.2:c.1037T>C	ENSP00000487062.1:p.Leu346Ser
ENST00000630858.2:c.1037T>C	ENSP00000486514.1:p.Leu346Ser
NM_001193416.2:c.1037T>C	NP_001180345.1:p.Leu346Ser
NM_001193417.2:c.989T>C	NP_001180346.1:p.Leu330Ser
NM_001356.4:c.1037T>C	NP_001347.3:p.Leu346Ser
NR_126093.1:n.1982T>C
XM_011543892.1:c.1037T>C	XP_011542194.1:p.Leu346Ser
NM_001363819.1:c.479T>C	NP_001350748.1:p.Leu160Ser
XM_011543892.2:c.1037T>C	XP_011542194.1:p.Leu346Ser
XM_017029313.1:c.479T>C	XP_016884802.1:p.Leu160Ser
NM_001193416.3:c.1037T>C	NP_001180345.1:p.Leu346Ser
NM_001193417.3:c.989T>C	NP_001180346.1:p.Leu330Ser
NM_001356.5:c.1037T>C MANE Select	NP_001347.3:p.Leu346Ser