Canonical Allele Identifier: CA412761507

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41193527A>C (hg19) ; chrX:g.41334274A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41334274A>C , CM000685.2:g.41334274A>C	GRCh38
NC_000023.10:g.41193527A>C , CM000685.1:g.41193527A>C	GRCh37
NC_000023.9:g.41078471A>C	NCBI36
NG_012830.1:g.5877A>C
NG_012830.2:g.5877A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399959.7:c.22A>C	ENSP00000382840.3:p.Asn8His
ENST00000441189.4:c.22A>C	ENSP00000414281.3:p.Asn8His
ENST00000457138.7:c.22A>C	ENSP00000392494.2:p.Asn8His
ENST00000480592.6:n.113A>C
ENST00000610559.5:n.436+491A>C
ENST00000611546.2:n.351+575A>C
ENST00000629496.3:c.22A>C	ENSP00000487224.1:p.Asn8His
ENST00000631641.2:n.113A>C
ENST00000642597.1:n.113A>C
ENST00000642624.1:n.18A>C
ENST00000642722.1:n.113A>C
ENST00000642793.1:c.22A>C	ENSP00000493976.1:p.Asn8His
ENST00000643821.1:c.22A>C	ENSP00000493997.1:p.Asn8His
ENST00000643963.1:c.22A>C	ENSP00000495264.1:p.Asn8His
ENST00000644074.1:c.22A>C	ENSP00000496663.1:p.Asn8His
ENST00000644109.1:c.22A>C	ENSP00000494952.1:p.Asn8His
ENST00000644307.1:n.113A>C
ENST00000644513.1:c.22A>C	ENSP00000493819.1:p.Asn8His
ENST00000644876.2:c.22A>C MANE Select	ENSP00000494040.1:p.Asn8His
ENST00000644958.1:n.113A>C
ENST00000645080.1:c.22A>C	ENSP00000494767.1:p.Asn8His
ENST00000645338.1:n.113A>C
ENST00000645561.1:n.113A>C
ENST00000645589.1:c.22A>C	ENSP00000494588.1:p.Asn8His
ENST00000645783.1:c.22A>C	ENSP00000494905.1:p.Asn8His
ENST00000646122.1:c.22A>C	ENSP00000496222.1:p.Asn8His
ENST00000646196.1:n.113A>C
ENST00000646223.1:c.22A>C	ENSP00000496043.1:p.Asn8His
ENST00000646319.1:c.22A>C	ENSP00000495377.1:p.Asn8His
ENST00000646822.1:n.113A>C
ENST00000646940.1:n.113A>C
ENST00000647219.1:n.113A>C
ENST00000399959.6:c.22A>C	ENSP00000382840.2:p.Asn8His
ENST00000441189.3:c.22A>C	ENSP00000414281.2:p.Asn8His
ENST00000457138.6:c.22A>C	ENSP00000392494.2:p.Asn8His
ENST00000478993.5:c.22A>C	ENSP00000478443.1:p.Asn8His
ENST00000480592.5:n.101A>C
ENST00000610559.4:n.436+491A>C
ENST00000615742.4:c.22A>C	ENSP00000480647.1:p.Asn8His
ENST00000625837.2:c.22A>C	ENSP00000486306.1:p.Asn8His
ENST00000626301.2:c.22A>C	ENSP00000486443.1:p.Asn8His
ENST00000629496.2:c.22A>C	ENSP00000487224.1:p.Asn8His
ENST00000629785.2:c.22A>C	ENSP00000486516.1:p.Asn8His
ENST00000630255.2:c.22A>C	ENSP00000486720.1:p.Asn8His
ENST00000630370.2:c.22A>C	ENSP00000487062.1:p.Asn8His
ENST00000630858.2:c.22A>C	ENSP00000486514.1:p.Asn8His
ENST00000631641.1:c.22A>C	ENSP00000488854.1:p.Asn8His
NM_001193416.2:c.22A>C	NP_001180345.1:p.Asn8His
NM_001193417.2:c.22A>C	NP_001180346.1:p.Asn8His
NM_001356.4:c.22A>C	NP_001347.3:p.Asn8His
NR_126093.1:n.967A>C
NR_126094.1:n.113A>C
XM_011543892.1:c.22A>C	XP_011542194.1:p.Asn8His
NM_001363819.1:c.-1882A>C	NP_001350748.1:n.-1882A>C
XM_011543892.2:c.22A>C	XP_011542194.1:p.Asn8His
XM_017029313.1:c.-1882A>C	XP_016884802.1:n.-1882A>C
XR_001755832.1:n.76+592T>G
XR_001755833.1:n.78+592T>G
XR_001755834.1:n.76+592T>G
XR_001755835.1:n.80+592T>G
NM_001193416.3:c.22A>C	NP_001180345.1:p.Asn8His
NM_001193417.3:c.22A>C	NP_001180346.1:p.Asn8His
NM_001356.5:c.22A>C MANE Select	NP_001347.3:p.Asn8His
NR_126094.2:n.113A>C