Canonical Allele Identifier: CA2693488130

Gene: DDX3X

Linked Data

• gnomAD v4: X-41341454-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41341458del , CM000685.2:g.41341458del	GRCh38
NC_000023.10:g.41200711del , CM000685.1:g.41200711del	GRCh37
NC_000023.9:g.41085655del	NCBI36
NG_012830.1:g.13061del
NG_012830.2:g.13061del

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.284-26del	ENSP00000496052.2:n.284-26del
ENST00000399959.7:c.149-26del	ENSP00000382840.3:n.149-26del
ENST00000441189.4:c.152-26del	ENSP00000414281.3:n.152-26del
ENST00000457138.7:c.104-26del	ENSP00000392494.2:n.104-26del
ENST00000610559.5:n.543-26del
ENST00000611546.2:n.458-26del
ENST00000615313.5:c.110-26del	ENSP00000496257.1:n.110-26del
ENST00000622198.5:n.309-26del
ENST00000629496.3:c.152-26del	ENSP00000487224.1:n.152-26del
ENST00000631641.2:n.195-26del
ENST00000642161.1:n.1447del
ENST00000642322.1:c.-407-26del	ENSP00000496052.1:n.-407-26del
ENST00000642424.1:c.-433del	ENSP00000496356.1:n.-433del
ENST00000642589.1:n.1516del
ENST00000642597.1:n.243-26del
ENST00000642624.1:n.42-26del
ENST00000642722.1:n.243-26del
ENST00000642763.1:n.139del
ENST00000642793.1:c.152-26del	ENSP00000493976.1:n.152-26del
ENST00000643963.1:c.152-26del	ENSP00000495264.1:n.152-26del
ENST00000644073.1:c.110-26del	ENSP00000493475.1:n.110-26del
ENST00000644074.1:c.149-26del	ENSP00000496663.1:n.149-26del
ENST00000644109.1:c.149-26del	ENSP00000494952.1:n.149-26del
ENST00000644307.1:n.243-26del
ENST00000644513.1:c.152-26del	ENSP00000493819.1:n.152-26del
ENST00000644677.1:c.35-26del	ENSP00000496524.1:n.35-26del
ENST00000644876.2:c.152-26del MANE Select	ENSP00000494040.1:n.152-26del
ENST00000644958.1:n.1813-26del
ENST00000645080.1:c.*1374-26del	ENSP00000494767.1:n.*1374-26del
ENST00000645120.1:n.1647-26del
ENST00000645253.1:n.1549del
ENST00000645338.1:n.243-26del
ENST00000645380.1:n.1511del
ENST00000645561.1:n.243-26del
ENST00000645574.1:n.1437del
ENST00000645589.1:c.152-26del	ENSP00000494588.1:n.152-26del
ENST00000645783.1:c.*1251-26del	ENSP00000494905.1:n.*1251-26del
ENST00000646107.1:c.35-26del	ENSP00000494518.1:n.35-26del
ENST00000646122.1:c.152-26del	ENSP00000496222.1:n.152-26del
ENST00000646196.1:n.243-26del
ENST00000646223.1:c.*145-26del	ENSP00000496043.1:n.*145-26del
ENST00000646319.1:c.152-26del	ENSP00000495377.1:n.152-26del
ENST00000646390.1:n.1453del
ENST00000646627.1:c.-407-26del	ENSP00000493795.1:n.-407-26del
ENST00000646679.1:c.-433del	ENSP00000494887.1:n.-433del
ENST00000646822.1:n.243-26del
ENST00000646940.1:n.243-26del
ENST00000647219.1:n.137-26del
ENST00000399959.6:c.152-26del	ENSP00000382840.2:n.152-26del
ENST00000441189.3:c.152-26del	ENSP00000414281.2:n.152-26del
ENST00000457138.6:c.104-26del	ENSP00000392494.2:n.104-26del
ENST00000478993.5:c.152-26del	ENSP00000478443.1:n.152-26del
ENST00000542215.5:n.286-26del
ENST00000611546.1:n.284-26del
ENST00000615313.4:n.388-26del
ENST00000615742.4:c.152-26del	ENSP00000480647.1:n.152-26del
ENST00000622198.4:n.253-26del
ENST00000625837.2:c.152-26del	ENSP00000486306.1:n.152-26del
ENST00000626301.2:c.152-26del	ENSP00000486443.1:n.152-26del
ENST00000629496.2:c.152-26del	ENSP00000487224.1:n.152-26del
ENST00000629785.2:c.152-26del	ENSP00000486516.1:n.152-26del
ENST00000630255.2:c.152-26del	ENSP00000486720.1:n.152-26del
ENST00000630370.2:c.152-26del	ENSP00000487062.1:n.152-26del
ENST00000630858.2:c.152-26del	ENSP00000486514.1:n.152-26del
ENST00000631641.1:c.104-26del	ENSP00000488854.1:n.104-26del
NM_001193416.2:c.152-26del	NP_001180345.1:n.152-26del
NM_001193417.2:c.104-26del	NP_001180346.1:n.104-26del
NM_001356.4:c.152-26del	NP_001347.3:n.152-26del
NR_126093.1:n.1097-26del
XM_011543892.1:c.152-26del	XP_011542194.1:n.152-26del
NM_001363819.1:c.-407-26del	NP_001350748.1:n.-407-26del
XM_011543892.2:c.152-26del	XP_011542194.1:n.152-26del
XM_017029313.1:c.-407-26del	XP_016884802.1:n.-407-26del
NM_001193416.3:c.152-26del	NP_001180345.1:n.152-26del
NM_001193417.3:c.104-26del	NP_001180346.1:n.104-26del
NM_001356.5:c.152-26del MANE Select	NP_001347.3:n.152-26del