Canonical Allele Identifier: CA2693488355

Gene: DDX3X

Linked Data

• gnomAD v4: X-41346653-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346659del , CM000685.2:g.41346659del	GRCh38
NC_000023.10:g.41205912del , CM000685.1:g.41205912del	GRCh37
NC_000023.9:g.41090856del	NCBI36
NG_012830.1:g.18262del
NG_012830.2:g.18262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1747+37del	ENSP00000496052.2:n.1747+37del
ENST00000399959.7:c.1612+37del	ENSP00000382840.3:n.1612+37del
ENST00000441189.4:c.1516+37del	ENSP00000414281.3:n.1516+37del
ENST00000457138.7:c.1567+37del	ENSP00000392494.2:n.1567+37del
ENST00000611968.2:c.209+37del
ENST00000616050.3:c.363+37del
ENST00000629496.3:c.1615+37del	ENSP00000487224.1:n.1615+37del
ENST00000642161.1:n.3814+37del
ENST00000642322.1:c.1057+37del	ENSP00000496052.1:n.1057+37del
ENST00000642424.1:c.1057+37del	ENSP00000496356.1:n.1057+37del
ENST00000642589.1:n.4937+37del
ENST00000642597.1:n.1789+37del
ENST00000642687.1:n.1648+37del
ENST00000642722.1:n.2448+37del
ENST00000642763.1:n.2506+37del
ENST00000642793.1:c.*1064+37del	ENSP00000493976.1:n.*1064+37del
ENST00000642801.1:n.1264+37del
ENST00000643820.1:n.985+37del
ENST00000643963.1:c.*897+37del	ENSP00000495264.1:n.*897+37del
ENST00000644073.1:c.1573+37del	ENSP00000493475.1:n.1573+37del
ENST00000644074.1:c.1612+37del	ENSP00000496663.1:n.1612+37del
ENST00000644109.1:c.1777+37del	ENSP00000494952.1:n.1777+37del
ENST00000644307.1:n.1785+37del
ENST00000644513.1:c.1615+37del	ENSP00000493819.1:n.1615+37del
ENST00000644677.1:c.1498+37del	ENSP00000496524.1:n.1498+37del
ENST00000644876.2:c.1615+37del MANE Select	ENSP00000494040.1:n.1615+37del
ENST00000644958.1:n.3276+37del
ENST00000645080.1:c.*2837+37del	ENSP00000494767.1:n.*2837+37del
ENST00000645120.1:n.3110+37del
ENST00000645338.1:n.1785+37del
ENST00000645380.1:n.3079+37del
ENST00000645561.1:n.2791+37del
ENST00000645574.1:n.4479+37del
ENST00000645589.1:c.*114+37del	ENSP00000494588.1:n.*114+37del
ENST00000646107.1:c.1498+37del	ENSP00000494518.1:n.1498+37del
ENST00000646122.1:c.1615+37del	ENSP00000496222.1:n.1615+37del
ENST00000646196.1:n.2584+37del
ENST00000646223.1:c.*1608+37del	ENSP00000496043.1:n.*1608+37del
ENST00000646319.1:c.1615+37del	ENSP00000495377.1:n.1615+37del
ENST00000646390.1:n.3903+37del
ENST00000646627.1:c.1057+37del	ENSP00000493795.1:n.1057+37del
ENST00000646679.1:c.1057+37del	ENSP00000494887.1:n.1057+37del
ENST00000646822.1:n.2677+37del
ENST00000646940.1:n.1789+37del
ENST00000647286.1:n.1713+37del
ENST00000647477.1:n.354+37del
ENST00000399959.6:c.1615+37del	ENSP00000382840.2:n.1615+37del
ENST00000441189.3:c.341-981del	ENSP00000414281.2:n.341-981del
ENST00000457138.6:c.1567+37del	ENSP00000392494.2:n.1567+37del
ENST00000478993.5:c.1615+37del	ENSP00000478443.1:n.1615+37del
ENST00000611968.1:c.57+37del
ENST00000616050.2:c.168+37del
ENST00000625837.2:c.1615+37del	ENSP00000486306.1:n.1615+37del
ENST00000626301.2:c.1615+37del	ENSP00000486443.1:n.1615+37del
ENST00000629496.2:c.1615+37del	ENSP00000487224.1:n.1615+37del
ENST00000629785.2:c.1615+37del	ENSP00000486516.1:n.1615+37del
ENST00000630255.2:c.1615+37del	ENSP00000486720.1:n.1615+37del
ENST00000630370.2:c.1615+37del	ENSP00000487062.1:n.1615+37del
ENST00000630858.2:c.1615+37del	ENSP00000486514.1:n.1615+37del
NM_001193416.2:c.1615+37del	NP_001180345.1:n.1615+37del
NM_001193417.2:c.1567+37del	NP_001180346.1:n.1567+37del
NM_001356.4:c.1615+37del	NP_001347.3:n.1615+37del
NR_126093.1:n.2560+37del
XM_011543892.1:c.1615+37del	XP_011542194.1:n.1615+37del
NM_001363819.1:c.1057+37del	NP_001350748.1:n.1057+37del
XM_011543892.2:c.1615+37del	XP_011542194.1:n.1615+37del
XM_017029313.1:c.1057+37del	XP_016884802.1:n.1057+37del
NM_001193416.3:c.1615+37del	NP_001180345.1:n.1615+37del
NM_001193417.3:c.1567+37del	NP_001180346.1:n.1567+37del
NM_001356.5:c.1615+37del MANE Select	NP_001347.3:n.1615+37del