Canonical Allele Identifier: CA2693488350

Gene: DDX3X

Linked Data

• gnomAD v4: X-41346626-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346626A>G , CM000685.2:g.41346626A>G	GRCh38
NC_000023.10:g.41205879A>G , CM000685.1:g.41205879A>G	GRCh37
NC_000023.9:g.41090823A>G	NCBI36
NG_012830.1:g.18229A>G
NG_012830.2:g.18229A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1747+4A>G	ENSP00000496052.2:n.1747+4A>G
ENST00000399959.7:c.1612+4A>G	ENSP00000382840.3:n.1612+4A>G
ENST00000441189.4:c.1516+4A>G	ENSP00000414281.3:n.1516+4A>G
ENST00000457138.7:c.1567+4A>G	ENSP00000392494.2:n.1567+4A>G
ENST00000611968.2:c.209+4A>G
ENST00000616050.3:c.363+4A>G
ENST00000629496.3:c.1615+4A>G	ENSP00000487224.1:n.1615+4A>G
ENST00000642161.1:n.3814+4A>G
ENST00000642322.1:c.1057+4A>G	ENSP00000496052.1:n.1057+4A>G
ENST00000642424.1:c.1057+4A>G	ENSP00000496356.1:n.1057+4A>G
ENST00000642589.1:n.4937+4A>G
ENST00000642597.1:n.1789+4A>G
ENST00000642687.1:n.1648+4A>G
ENST00000642722.1:n.2448+4A>G
ENST00000642763.1:n.2506+4A>G
ENST00000642793.1:c.*1064+4A>G	ENSP00000493976.1:n.*1064+4A>G
ENST00000642801.1:n.1264+4A>G
ENST00000643820.1:n.985+4A>G
ENST00000643963.1:c.*897+4A>G	ENSP00000495264.1:n.*897+4A>G
ENST00000644073.1:c.1573+4A>G	ENSP00000493475.1:n.1573+4A>G
ENST00000644074.1:c.1612+4A>G	ENSP00000496663.1:n.1612+4A>G
ENST00000644109.1:c.1777+4A>G	ENSP00000494952.1:n.1777+4A>G
ENST00000644307.1:n.1785+4A>G
ENST00000644513.1:c.1615+4A>G	ENSP00000493819.1:n.1615+4A>G
ENST00000644677.1:c.1498+4A>G	ENSP00000496524.1:n.1498+4A>G
ENST00000644876.2:c.1615+4A>G MANE Select	ENSP00000494040.1:n.1615+4A>G
ENST00000644958.1:n.3276+4A>G
ENST00000645080.1:c.*2837+4A>G	ENSP00000494767.1:n.*2837+4A>G
ENST00000645120.1:n.3110+4A>G
ENST00000645338.1:n.1785+4A>G
ENST00000645380.1:n.3079+4A>G
ENST00000645561.1:n.2791+4A>G
ENST00000645574.1:n.4479+4A>G
ENST00000645589.1:c.*114+4A>G	ENSP00000494588.1:n.*114+4A>G
ENST00000646107.1:c.1498+4A>G	ENSP00000494518.1:n.1498+4A>G
ENST00000646122.1:c.1615+4A>G	ENSP00000496222.1:n.1615+4A>G
ENST00000646196.1:n.2584+4A>G
ENST00000646223.1:c.*1608+4A>G	ENSP00000496043.1:n.*1608+4A>G
ENST00000646319.1:c.1615+4A>G	ENSP00000495377.1:n.1615+4A>G
ENST00000646390.1:n.3903+4A>G
ENST00000646627.1:c.1057+4A>G	ENSP00000493795.1:n.1057+4A>G
ENST00000646679.1:c.1057+4A>G	ENSP00000494887.1:n.1057+4A>G
ENST00000646822.1:n.2677+4A>G
ENST00000646940.1:n.1789+4A>G
ENST00000647286.1:n.1713+4A>G
ENST00000647477.1:n.354+4A>G
ENST00000399959.6:c.1615+4A>G	ENSP00000382840.2:n.1615+4A>G
ENST00000441189.3:c.341-1014A>G	ENSP00000414281.2:n.341-1014A>G
ENST00000457138.6:c.1567+4A>G	ENSP00000392494.2:n.1567+4A>G
ENST00000478993.5:c.1615+4A>G	ENSP00000478443.1:n.1615+4A>G
ENST00000611968.1:c.57+4A>G
ENST00000616050.2:c.168+4A>G
ENST00000625837.2:c.1615+4A>G	ENSP00000486306.1:n.1615+4A>G
ENST00000626301.2:c.1615+4A>G	ENSP00000486443.1:n.1615+4A>G
ENST00000629496.2:c.1615+4A>G	ENSP00000487224.1:n.1615+4A>G
ENST00000629785.2:c.1615+4A>G	ENSP00000486516.1:n.1615+4A>G
ENST00000630255.2:c.1615+4A>G	ENSP00000486720.1:n.1615+4A>G
ENST00000630370.2:c.1615+4A>G	ENSP00000487062.1:n.1615+4A>G
ENST00000630858.2:c.1615+4A>G	ENSP00000486514.1:n.1615+4A>G
NM_001193416.2:c.1615+4A>G	NP_001180345.1:n.1615+4A>G
NM_001193417.2:c.1567+4A>G	NP_001180346.1:n.1567+4A>G
NM_001356.4:c.1615+4A>G	NP_001347.3:n.1615+4A>G
NR_126093.1:n.2560+4A>G
XM_011543892.1:c.1615+4A>G	XP_011542194.1:n.1615+4A>G
NM_001363819.1:c.1057+4A>G	NP_001350748.1:n.1057+4A>G
XM_011543892.2:c.1615+4A>G	XP_011542194.1:n.1615+4A>G
XM_017029313.1:c.1057+4A>G	XP_016884802.1:n.1057+4A>G
NM_001193416.3:c.1615+4A>G	NP_001180345.1:n.1615+4A>G
NM_001193417.3:c.1567+4A>G	NP_001180346.1:n.1567+4A>G
NM_001356.5:c.1615+4A>G MANE Select	NP_001347.3:n.1615+4A>G