Canonical Allele Identifier: CA412775501

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205609A>C (hg19) ; chrX:g.41346356A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346356A>C , CM000685.2:g.41346356A>C	GRCh38
NC_000023.10:g.41205609A>C , CM000685.1:g.41205609A>C	GRCh37
NC_000023.9:g.41090553A>C	NCBI36
NG_012830.1:g.17959A>C
NG_012830.2:g.17959A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1575A>C	ENSP00000496052.2:p.Glu525Asp
ENST00000399959.7:c.1440A>C	ENSP00000382840.3:p.Glu480Asp
ENST00000441189.4:c.1344A>C	ENSP00000414281.3:p.Glu448Asp
ENST00000457138.7:c.1395A>C	ENSP00000392494.2:p.Glu465Asp
ENST00000611968.2:c.37A>C
ENST00000616050.3:c.191A>C
ENST00000629496.3:c.1443A>C	ENSP00000487224.1:p.Glu481Asp
ENST00000642161.1:n.3642A>C
ENST00000642322.1:c.885A>C	ENSP00000496052.1:p.Glu295Asp
ENST00000642424.1:c.885A>C	ENSP00000496356.1:p.Glu295Asp
ENST00000642589.1:n.4765A>C
ENST00000642597.1:n.1617A>C
ENST00000642687.1:n.1476A>C
ENST00000642722.1:n.2276A>C
ENST00000642763.1:n.2334A>C
ENST00000642793.1:c.*892A>C	ENSP00000493976.1:n.*892A>C
ENST00000642801.1:n.1092A>C
ENST00000643820.1:n.719A>C
ENST00000643963.1:c.*725A>C	ENSP00000495264.1:n.*725A>C
ENST00000644073.1:c.1401A>C	ENSP00000493475.1:p.Glu467Asp
ENST00000644074.1:c.1440A>C	ENSP00000496663.1:p.Glu480Asp
ENST00000644109.1:c.1605A>C	ENSP00000494952.1:p.Glu535Asp
ENST00000644307.1:n.1613A>C
ENST00000644513.1:c.1443A>C	ENSP00000493819.1:p.Glu481Asp
ENST00000644677.1:c.1326A>C	ENSP00000496524.1:p.Glu442Asp
ENST00000644876.2:c.1443A>C MANE Select	ENSP00000494040.1:p.Glu481Asp
ENST00000644958.1:n.3104A>C
ENST00000645080.1:c.*2665A>C	ENSP00000494767.1:n.*2665A>C
ENST00000645120.1:n.2938A>C
ENST00000645338.1:n.1613A>C
ENST00000645380.1:n.2907A>C
ENST00000645561.1:n.2619A>C
ENST00000645574.1:n.4307A>C
ENST00000645589.1:c.1443A>C	ENSP00000494588.1:p.Glu481Asp
ENST00000646107.1:c.1326A>C	ENSP00000494518.1:p.Glu442Asp
ENST00000646122.1:c.1443A>C	ENSP00000496222.1:p.Glu481Asp
ENST00000646196.1:n.2412A>C
ENST00000646223.1:c.*1436A>C	ENSP00000496043.1:n.*1436A>C
ENST00000646319.1:c.1443A>C	ENSP00000495377.1:p.Glu481Asp
ENST00000646390.1:n.3731A>C
ENST00000646627.1:c.885A>C	ENSP00000493795.1:p.Glu295Asp
ENST00000646679.1:c.885A>C	ENSP00000494887.1:p.Glu295Asp
ENST00000646822.1:n.2505A>C
ENST00000646940.1:n.1617A>C
ENST00000647286.1:n.1541A>C
ENST00000647477.1:n.182A>C
ENST00000399959.6:c.1443A>C	ENSP00000382840.2:p.Glu481Asp
ENST00000441189.3:c.341-1284A>C	ENSP00000414281.2:n.341-1284A>C
ENST00000457138.6:c.1395A>C	ENSP00000392494.2:p.Glu465Asp
ENST00000478993.5:c.1443A>C	ENSP00000478443.1:p.Glu481Asp
ENST00000542215.5:n.1491A>C
ENST00000625837.2:c.1443A>C	ENSP00000486306.1:p.Glu481Asp
ENST00000626301.2:c.1443A>C	ENSP00000486443.1:p.Glu481Asp
ENST00000629496.2:c.1443A>C	ENSP00000487224.1:p.Glu481Asp
ENST00000629785.2:c.1443A>C	ENSP00000486516.1:p.Glu481Asp
ENST00000630255.2:c.1443A>C	ENSP00000486720.1:p.Glu481Asp
ENST00000630370.2:c.1443A>C	ENSP00000487062.1:p.Glu481Asp
ENST00000630858.2:c.1443A>C	ENSP00000486514.1:p.Glu481Asp
NM_001193416.2:c.1443A>C	NP_001180345.1:p.Glu481Asp
NM_001193417.2:c.1395A>C	NP_001180346.1:p.Glu465Asp
NM_001356.4:c.1443A>C	NP_001347.3:p.Glu481Asp
NR_126093.1:n.2388A>C
XM_011543892.1:c.1443A>C	XP_011542194.1:p.Glu481Asp
NM_001363819.1:c.885A>C	NP_001350748.1:p.Glu295Asp
XM_011543892.2:c.1443A>C	XP_011542194.1:p.Glu481Asp
XM_017029313.1:c.885A>C	XP_016884802.1:p.Glu295Asp
NM_001193416.3:c.1443A>C	NP_001180345.1:p.Glu481Asp
NM_001193417.3:c.1395A>C	NP_001180346.1:p.Glu465Asp
NM_001356.5:c.1443A>C MANE Select	NP_001347.3:p.Glu481Asp