Canonical Allele Identifier: CA2693487983

Gene: DDX3X

Linked Data

• gnomAD v4: X-41345345-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345345T>C , CM000685.2:g.41345345T>C	GRCh38
NC_000023.10:g.41204598T>C , CM000685.1:g.41204598T>C	GRCh37
NC_000023.9:g.41089542T>C	NCBI36
NG_012830.1:g.16948T>C
NG_012830.2:g.16948T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1302+21T>C	ENSP00000496052.2:n.1302+21T>C
ENST00000399959.7:c.1167+21T>C	ENSP00000382840.3:n.1167+21T>C
ENST00000441189.4:c.1071+21T>C	ENSP00000414281.3:n.1071+21T>C
ENST00000457138.7:c.1122+21T>C	ENSP00000392494.2:n.1122+21T>C
ENST00000629496.3:c.1170+21T>C	ENSP00000487224.1:n.1170+21T>C
ENST00000642161.1:n.3369+21T>C
ENST00000642322.1:c.612+21T>C	ENSP00000496052.1:n.612+21T>C
ENST00000642424.1:c.612+21T>C	ENSP00000496356.1:n.612+21T>C
ENST00000642589.1:n.4492+21T>C
ENST00000642597.1:n.1344+21T>C
ENST00000642687.1:n.1203+21T>C
ENST00000642722.1:n.2003+21T>C
ENST00000642763.1:n.2061+21T>C
ENST00000642793.1:c.*619+21T>C	ENSP00000493976.1:n.*619+21T>C
ENST00000642801.1:n.819+21T>C
ENST00000643820.1:n.446+21T>C
ENST00000643963.1:c.*452+21T>C	ENSP00000495264.1:n.*452+21T>C
ENST00000644073.1:c.1128+21T>C	ENSP00000493475.1:n.1128+21T>C
ENST00000644074.1:c.1167+21T>C	ENSP00000496663.1:n.1167+21T>C
ENST00000644109.1:c.1332+21T>C	ENSP00000494952.1:n.1332+21T>C
ENST00000644307.1:n.1282T>C
ENST00000644513.1:c.1170+21T>C	ENSP00000493819.1:n.1170+21T>C
ENST00000644677.1:c.1053+21T>C	ENSP00000496524.1:n.1053+21T>C
ENST00000644876.2:c.1170+21T>C MANE Select	ENSP00000494040.1:n.1170+21T>C
ENST00000644958.1:n.2831+21T>C
ENST00000645080.1:c.*2392+21T>C	ENSP00000494767.1:n.*2392+21T>C
ENST00000645120.1:n.2665+21T>C
ENST00000645338.1:n.1282T>C
ENST00000645380.1:n.2576T>C
ENST00000645561.1:n.2346+21T>C
ENST00000645574.1:n.4034+21T>C
ENST00000645589.1:c.1170+21T>C	ENSP00000494588.1:n.1170+21T>C
ENST00000646093.1:n.354+21T>C
ENST00000646107.1:c.1053+21T>C	ENSP00000494518.1:n.1053+21T>C
ENST00000646122.1:c.1170+21T>C	ENSP00000496222.1:n.1170+21T>C
ENST00000646196.1:n.2139+21T>C
ENST00000646223.1:c.*1163+21T>C	ENSP00000496043.1:n.*1163+21T>C
ENST00000646319.1:c.1170+21T>C	ENSP00000495377.1:n.1170+21T>C
ENST00000646390.1:n.3458+21T>C
ENST00000646627.1:c.612+21T>C	ENSP00000493795.1:n.612+21T>C
ENST00000646679.1:c.612+21T>C	ENSP00000494887.1:n.612+21T>C
ENST00000646822.1:n.2232+21T>C
ENST00000646940.1:n.1344+21T>C
ENST00000647286.1:n.1268+21T>C
ENST00000399959.6:c.1170+21T>C	ENSP00000382840.2:n.1170+21T>C
ENST00000441189.3:c.341-2295T>C	ENSP00000414281.2:n.341-2295T>C
ENST00000457138.6:c.1122+21T>C	ENSP00000392494.2:n.1122+21T>C
ENST00000478993.5:c.1170+21T>C	ENSP00000478443.1:n.1170+21T>C
ENST00000542215.5:n.1218+21T>C
ENST00000625837.2:c.1170+21T>C	ENSP00000486306.1:n.1170+21T>C
ENST00000626301.2:c.1170+21T>C	ENSP00000486443.1:n.1170+21T>C
ENST00000629496.2:c.1170+21T>C	ENSP00000487224.1:n.1170+21T>C
ENST00000629785.2:c.1170+21T>C	ENSP00000486516.1:n.1170+21T>C
ENST00000630255.2:c.1170+21T>C	ENSP00000486720.1:n.1170+21T>C
ENST00000630370.2:c.1170+21T>C	ENSP00000487062.1:n.1170+21T>C
ENST00000630858.2:c.1170+21T>C	ENSP00000486514.1:n.1170+21T>C
NM_001193416.2:c.1170+21T>C	NP_001180345.1:n.1170+21T>C
NM_001193417.2:c.1122+21T>C	NP_001180346.1:n.1122+21T>C
NM_001356.4:c.1170+21T>C	NP_001347.3:n.1170+21T>C
NR_126093.1:n.2115+21T>C
XM_011543892.1:c.1170+21T>C	XP_011542194.1:n.1170+21T>C
NM_001363819.1:c.612+21T>C	NP_001350748.1:n.612+21T>C
XM_011543892.2:c.1170+21T>C	XP_011542194.1:n.1170+21T>C
XM_017029313.1:c.612+21T>C	XP_016884802.1:n.612+21T>C
NM_001193416.3:c.1170+21T>C	NP_001180345.1:n.1170+21T>C
NM_001193417.3:c.1122+21T>C	NP_001180346.1:n.1122+21T>C
NM_001356.5:c.1170+21T>C MANE Select	NP_001347.3:n.1170+21T>C