Canonical Allele Identifier: CA412773785

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204803T>C (hg19) ; chrX:g.41345550T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345550T>C , CM000685.2:g.41345550T>C	GRCh38
NC_000023.10:g.41204803T>C , CM000685.1:g.41204803T>C	GRCh37
NC_000023.9:g.41089747T>C	NCBI36
NG_012830.1:g.17153T>C
NG_012830.2:g.17153T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1447+2T>C	ENSP00000496052.2:n.1447+2T>C
ENST00000399959.7:c.1312+2T>C	ENSP00000382840.3:n.1312+2T>C
ENST00000441189.4:c.1216+2T>C	ENSP00000414281.3:n.1216+2T>C
ENST00000457138.7:c.1267+2T>C	ENSP00000392494.2:n.1267+2T>C
ENST00000616050.3:c.63+2T>C
ENST00000629496.3:c.1315+2T>C	ENSP00000487224.1:n.1315+2T>C
ENST00000642161.1:n.3514+2T>C
ENST00000642322.1:c.757+2T>C	ENSP00000496052.1:n.757+2T>C
ENST00000642424.1:c.757+2T>C	ENSP00000496356.1:n.757+2T>C
ENST00000642589.1:n.4637+2T>C
ENST00000642597.1:n.1489+2T>C
ENST00000642687.1:n.1348+2T>C
ENST00000642722.1:n.2148+2T>C
ENST00000642763.1:n.2206+2T>C
ENST00000642793.1:c.*764+2T>C	ENSP00000493976.1:n.*764+2T>C
ENST00000642801.1:n.964+2T>C
ENST00000643820.1:n.591+2T>C
ENST00000643963.1:c.*597+2T>C	ENSP00000495264.1:n.*597+2T>C
ENST00000644073.1:c.1273+2T>C	ENSP00000493475.1:n.1273+2T>C
ENST00000644074.1:c.1312+2T>C	ENSP00000496663.1:n.1312+2T>C
ENST00000644109.1:c.1477+2T>C	ENSP00000494952.1:n.1477+2T>C
ENST00000644307.1:n.1485+2T>C
ENST00000644513.1:c.1315+2T>C	ENSP00000493819.1:n.1315+2T>C
ENST00000644677.1:c.1198+2T>C	ENSP00000496524.1:n.1198+2T>C
ENST00000644876.2:c.1315+2T>C MANE Select	ENSP00000494040.1:n.1315+2T>C
ENST00000644958.1:n.2976+2T>C
ENST00000645080.1:c.*2537+2T>C	ENSP00000494767.1:n.*2537+2T>C
ENST00000645120.1:n.2810+2T>C
ENST00000645338.1:n.1485+2T>C
ENST00000645380.1:n.2779+2T>C
ENST00000645561.1:n.2491+2T>C
ENST00000645574.1:n.4179+2T>C
ENST00000645589.1:c.1315+2T>C	ENSP00000494588.1:n.1315+2T>C
ENST00000646093.1:n.499+2T>C
ENST00000646107.1:c.1198+2T>C	ENSP00000494518.1:n.1198+2T>C
ENST00000646122.1:c.1315+2T>C	ENSP00000496222.1:n.1315+2T>C
ENST00000646196.1:n.2284+2T>C
ENST00000646223.1:c.*1308+2T>C	ENSP00000496043.1:n.*1308+2T>C
ENST00000646319.1:c.1315+2T>C	ENSP00000495377.1:n.1315+2T>C
ENST00000646390.1:n.3603+2T>C
ENST00000646627.1:c.757+2T>C	ENSP00000493795.1:n.757+2T>C
ENST00000646679.1:c.757+2T>C	ENSP00000494887.1:n.757+2T>C
ENST00000646822.1:n.2377+2T>C
ENST00000646940.1:n.1489+2T>C
ENST00000647286.1:n.1413+2T>C
ENST00000647477.1:n.54+2T>C
ENST00000399959.6:c.1315+2T>C	ENSP00000382840.2:n.1315+2T>C
ENST00000441189.3:c.341-2090T>C	ENSP00000414281.2:n.341-2090T>C
ENST00000457138.6:c.1267+2T>C	ENSP00000392494.2:n.1267+2T>C
ENST00000478993.5:c.1315+2T>C	ENSP00000478443.1:n.1315+2T>C
ENST00000542215.5:n.1363+2T>C
ENST00000625837.2:c.1315+2T>C	ENSP00000486306.1:n.1315+2T>C
ENST00000626301.2:c.1315+2T>C	ENSP00000486443.1:n.1315+2T>C
ENST00000629496.2:c.1315+2T>C	ENSP00000487224.1:n.1315+2T>C
ENST00000629785.2:c.1315+2T>C	ENSP00000486516.1:n.1315+2T>C
ENST00000630255.2:c.1315+2T>C	ENSP00000486720.1:n.1315+2T>C
ENST00000630370.2:c.1315+2T>C	ENSP00000487062.1:n.1315+2T>C
ENST00000630858.2:c.1315+2T>C	ENSP00000486514.1:n.1315+2T>C
NM_001193416.2:c.1315+2T>C	NP_001180345.1:n.1315+2T>C
NM_001193417.2:c.1267+2T>C	NP_001180346.1:n.1267+2T>C
NM_001356.4:c.1315+2T>C	NP_001347.3:n.1315+2T>C
NR_126093.1:n.2260+2T>C
XM_011543892.1:c.1315+2T>C	XP_011542194.1:n.1315+2T>C
NM_001363819.1:c.757+2T>C	NP_001350748.1:n.757+2T>C
XM_011543892.2:c.1315+2T>C	XP_011542194.1:n.1315+2T>C
XM_017029313.1:c.757+2T>C	XP_016884802.1:n.757+2T>C
NM_001193416.3:c.1315+2T>C	NP_001180345.1:n.1315+2T>C
NM_001193417.3:c.1267+2T>C	NP_001180346.1:n.1267+2T>C
NM_001356.5:c.1315+2T>C MANE Select	NP_001347.3:n.1315+2T>C