Canonical Allele Identifier: CA516347230

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204464T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345211T>C , CM000685.2:g.41345211T>C	GRCh38
NC_000023.10:g.41204464T>C , CM000685.1:g.41204464T>C	GRCh37
NC_000023.9:g.41089408T>C	NCBI36
NG_012830.1:g.16814T>C
NG_012830.2:g.16814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1189T>C	ENSP00000496052.2:p.Leu397=
ENST00000399959.7:c.1054T>C	ENSP00000382840.3:p.Leu352=
ENST00000441189.4:c.958T>C	ENSP00000414281.3:p.Leu320=
ENST00000457138.7:c.1009T>C	ENSP00000392494.2:p.Leu337=
ENST00000629496.3:c.1057T>C	ENSP00000487224.1:p.Leu353=
ENST00000642161.1:n.3256T>C
ENST00000642322.1:c.499T>C	ENSP00000496052.1:p.Leu167=
ENST00000642424.1:c.499T>C	ENSP00000496356.1:p.Leu167=
ENST00000642589.1:n.4379T>C
ENST00000642597.1:n.1231T>C
ENST00000642687.1:n.1090T>C
ENST00000642722.1:n.1890T>C
ENST00000642763.1:n.1948T>C
ENST00000642793.1:c.*506T>C	ENSP00000493976.1:n.*506T>C
ENST00000642801.1:n.706T>C
ENST00000643820.1:n.333T>C
ENST00000643963.1:c.*339T>C	ENSP00000495264.1:n.*339T>C
ENST00000644073.1:c.1015T>C	ENSP00000493475.1:p.Leu339=
ENST00000644074.1:c.1054T>C	ENSP00000496663.1:p.Leu352=
ENST00000644109.1:c.1219T>C	ENSP00000494952.1:p.Leu407=
ENST00000644307.1:n.1148T>C
ENST00000644513.1:c.1057T>C	ENSP00000493819.1:p.Leu353=
ENST00000644677.1:c.940T>C	ENSP00000496524.1:p.Leu314=
ENST00000644876.2:c.1057T>C MANE Select	ENSP00000494040.1:p.Leu353=
ENST00000644958.1:n.2718T>C
ENST00000645080.1:c.*2279T>C	ENSP00000494767.1:n.*2279T>C
ENST00000645120.1:n.2552T>C
ENST00000645338.1:n.1148T>C
ENST00000645380.1:n.2442T>C
ENST00000645561.1:n.2233T>C
ENST00000645574.1:n.3921T>C
ENST00000645589.1:c.1057T>C	ENSP00000494588.1:p.Leu353=
ENST00000646093.1:n.241T>C
ENST00000646107.1:c.940T>C	ENSP00000494518.1:p.Leu314=
ENST00000646122.1:c.1057T>C	ENSP00000496222.1:p.Leu353=
ENST00000646196.1:n.2026T>C
ENST00000646223.1:c.*1050T>C	ENSP00000496043.1:n.*1050T>C
ENST00000646319.1:c.1057T>C	ENSP00000495377.1:p.Leu353=
ENST00000646390.1:n.3345T>C
ENST00000646627.1:c.499T>C	ENSP00000493795.1:p.Leu167=
ENST00000646679.1:c.499T>C	ENSP00000494887.1:p.Leu167=
ENST00000646822.1:n.2119T>C
ENST00000646940.1:n.1231T>C
ENST00000647286.1:n.1155T>C
ENST00000399959.6:c.1057T>C	ENSP00000382840.2:p.Leu353=
ENST00000441189.3:c.341-2429T>C	ENSP00000414281.2:n.341-2429T>C
ENST00000457138.6:c.1009T>C	ENSP00000392494.2:p.Leu337=
ENST00000478993.5:c.1057T>C	ENSP00000478443.1:p.Leu353=
ENST00000542215.5:n.1105T>C
ENST00000625837.2:c.1057T>C	ENSP00000486306.1:p.Leu353=
ENST00000626301.2:c.1057T>C	ENSP00000486443.1:p.Leu353=
ENST00000629496.2:c.1057T>C	ENSP00000487224.1:p.Leu353=
ENST00000629785.2:c.1057T>C	ENSP00000486516.1:p.Leu353=
ENST00000630255.2:c.1057T>C	ENSP00000486720.1:p.Leu353=
ENST00000630370.2:c.1057T>C	ENSP00000487062.1:p.Leu353=
ENST00000630858.2:c.1057T>C	ENSP00000486514.1:p.Leu353=
NM_001193416.2:c.1057T>C	NP_001180345.1:p.Leu353=
NM_001193417.2:c.1009T>C	NP_001180346.1:p.Leu337=
NM_001356.4:c.1057T>C	NP_001347.3:p.Leu353=
NR_126093.1:n.2002T>C
XM_011543892.1:c.1057T>C	XP_011542194.1:p.Leu353=
NM_001363819.1:c.499T>C	NP_001350748.1:p.Leu167=
XM_011543892.2:c.1057T>C	XP_011542194.1:p.Leu353=
XM_017029313.1:c.499T>C	XP_016884802.1:p.Leu167=
NM_001193416.3:c.1057T>C	NP_001180345.1:p.Leu353=
NM_001193417.3:c.1009T>C	NP_001180346.1:p.Leu337=
NM_001356.5:c.1057T>C MANE Select	NP_001347.3:p.Leu353=