Canonical Allele Identifier: CA412774331

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205518A>C (hg19) ; chrX:g.41346265A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346265A>C , CM000685.2:g.41346265A>C	GRCh38
NC_000023.10:g.41205518A>C , CM000685.1:g.41205518A>C	GRCh37
NC_000023.9:g.41090462A>C	NCBI36
NG_012830.1:g.17868A>C
NG_012830.2:g.17868A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1484A>C	ENSP00000496052.2:p.Lys495Thr
ENST00000399959.7:c.1349A>C	ENSP00000382840.3:p.Lys450Thr
ENST00000441189.4:c.1253A>C	ENSP00000414281.3:p.Lys418Thr
ENST00000457138.7:c.1304A>C	ENSP00000392494.2:p.Lys435Thr
ENST00000616050.3:c.100A>C
ENST00000629496.3:c.1352A>C	ENSP00000487224.1:p.Lys451Thr
ENST00000642161.1:n.3551A>C
ENST00000642322.1:c.794A>C	ENSP00000496052.1:p.Lys265Thr
ENST00000642424.1:c.794A>C	ENSP00000496356.1:p.Lys265Thr
ENST00000642589.1:n.4674A>C
ENST00000642597.1:n.1526A>C
ENST00000642687.1:n.1385A>C
ENST00000642722.1:n.2185A>C
ENST00000642763.1:n.2243A>C
ENST00000642793.1:c.*801A>C	ENSP00000493976.1:n.*801A>C
ENST00000642801.1:n.1001A>C
ENST00000643820.1:n.628A>C
ENST00000643963.1:c.*634A>C	ENSP00000495264.1:n.*634A>C
ENST00000644073.1:c.1310A>C	ENSP00000493475.1:p.Lys437Thr
ENST00000644074.1:c.1349A>C	ENSP00000496663.1:p.Lys450Thr
ENST00000644109.1:c.1514A>C	ENSP00000494952.1:p.Lys505Thr
ENST00000644307.1:n.1522A>C
ENST00000644513.1:c.1352A>C	ENSP00000493819.1:p.Lys451Thr
ENST00000644677.1:c.1235A>C	ENSP00000496524.1:p.Lys412Thr
ENST00000644876.2:c.1352A>C MANE Select	ENSP00000494040.1:p.Lys451Thr
ENST00000644958.1:n.3013A>C
ENST00000645080.1:c.*2574A>C	ENSP00000494767.1:n.*2574A>C
ENST00000645120.1:n.2847A>C
ENST00000645338.1:n.1522A>C
ENST00000645380.1:n.2816A>C
ENST00000645561.1:n.2528A>C
ENST00000645574.1:n.4216A>C
ENST00000645589.1:c.1352A>C	ENSP00000494588.1:p.Lys451Thr
ENST00000646107.1:c.1235A>C	ENSP00000494518.1:p.Lys412Thr
ENST00000646122.1:c.1352A>C	ENSP00000496222.1:p.Lys451Thr
ENST00000646196.1:n.2321A>C
ENST00000646223.1:c.*1345A>C	ENSP00000496043.1:n.*1345A>C
ENST00000646319.1:c.1352A>C	ENSP00000495377.1:p.Lys451Thr
ENST00000646390.1:n.3640A>C
ENST00000646627.1:c.794A>C	ENSP00000493795.1:p.Lys265Thr
ENST00000646679.1:c.794A>C	ENSP00000494887.1:p.Lys265Thr
ENST00000646822.1:n.2414A>C
ENST00000646940.1:n.1526A>C
ENST00000647286.1:n.1450A>C
ENST00000647477.1:n.91A>C
ENST00000399959.6:c.1352A>C	ENSP00000382840.2:p.Lys451Thr
ENST00000441189.3:c.341-1375A>C	ENSP00000414281.2:n.341-1375A>C
ENST00000457138.6:c.1304A>C	ENSP00000392494.2:p.Lys435Thr
ENST00000478993.5:c.1352A>C	ENSP00000478443.1:p.Lys451Thr
ENST00000542215.5:n.1400A>C
ENST00000625837.2:c.1352A>C	ENSP00000486306.1:p.Lys451Thr
ENST00000626301.2:c.1352A>C	ENSP00000486443.1:p.Lys451Thr
ENST00000629496.2:c.1352A>C	ENSP00000487224.1:p.Lys451Thr
ENST00000629785.2:c.1352A>C	ENSP00000486516.1:p.Lys451Thr
ENST00000630255.2:c.1352A>C	ENSP00000486720.1:p.Lys451Thr
ENST00000630370.2:c.1352A>C	ENSP00000487062.1:p.Lys451Thr
ENST00000630858.2:c.1352A>C	ENSP00000486514.1:p.Lys451Thr
NM_001193416.2:c.1352A>C	NP_001180345.1:p.Lys451Thr
NM_001193417.2:c.1304A>C	NP_001180346.1:p.Lys435Thr
NM_001356.4:c.1352A>C	NP_001347.3:p.Lys451Thr
NR_126093.1:n.2297A>C
XM_011543892.1:c.1352A>C	XP_011542194.1:p.Lys451Thr
NM_001363819.1:c.794A>C	NP_001350748.1:p.Lys265Thr
XM_011543892.2:c.1352A>C	XP_011542194.1:p.Lys451Thr
XM_017029313.1:c.794A>C	XP_016884802.1:p.Lys265Thr
NM_001193416.3:c.1352A>C	NP_001180345.1:p.Lys451Thr
NM_001193417.3:c.1304A>C	NP_001180346.1:p.Lys435Thr
NM_001356.5:c.1352A>C MANE Select	NP_001347.3:p.Lys451Thr