Canonical Allele Identifier: CA412775138

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205575G>C (hg19) ; chrX:g.41346322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346322G>C , CM000685.2:g.41346322G>C	GRCh38
NC_000023.10:g.41205575G>C , CM000685.1:g.41205575G>C	GRCh37
NC_000023.9:g.41090519G>C	NCBI36
NG_012830.1:g.17925G>C
NG_012830.2:g.17925G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1541G>C	ENSP00000496052.2:p.Ser514Thr
ENST00000399959.7:c.1406G>C	ENSP00000382840.3:p.Ser469Thr
ENST00000441189.4:c.1310G>C	ENSP00000414281.3:p.Ser437Thr
ENST00000457138.7:c.1361G>C	ENSP00000392494.2:p.Ser454Thr
ENST00000611968.2:c.3G>C
ENST00000616050.3:c.157G>C
ENST00000629496.3:c.1409G>C	ENSP00000487224.1:p.Ser470Thr
ENST00000642161.1:n.3608G>C
ENST00000642322.1:c.851G>C	ENSP00000496052.1:p.Ser284Thr
ENST00000642424.1:c.851G>C	ENSP00000496356.1:p.Ser284Thr
ENST00000642589.1:n.4731G>C
ENST00000642597.1:n.1583G>C
ENST00000642687.1:n.1442G>C
ENST00000642722.1:n.2242G>C
ENST00000642763.1:n.2300G>C
ENST00000642793.1:c.*858G>C	ENSP00000493976.1:n.*858G>C
ENST00000642801.1:n.1058G>C
ENST00000643820.1:n.685G>C
ENST00000643963.1:c.*691G>C	ENSP00000495264.1:n.*691G>C
ENST00000644073.1:c.1367G>C	ENSP00000493475.1:p.Ser456Thr
ENST00000644074.1:c.1406G>C	ENSP00000496663.1:p.Ser469Thr
ENST00000644109.1:c.1571G>C	ENSP00000494952.1:p.Ser524Thr
ENST00000644307.1:n.1579G>C
ENST00000644513.1:c.1409G>C	ENSP00000493819.1:p.Ser470Thr
ENST00000644677.1:c.1292G>C	ENSP00000496524.1:p.Ser431Thr
ENST00000644876.2:c.1409G>C MANE Select	ENSP00000494040.1:p.Ser470Thr
ENST00000644958.1:n.3070G>C
ENST00000645080.1:c.*2631G>C	ENSP00000494767.1:n.*2631G>C
ENST00000645120.1:n.2904G>C
ENST00000645338.1:n.1579G>C
ENST00000645380.1:n.2873G>C
ENST00000645561.1:n.2585G>C
ENST00000645574.1:n.4273G>C
ENST00000645589.1:c.1409G>C	ENSP00000494588.1:p.Ser470Thr
ENST00000646107.1:c.1292G>C	ENSP00000494518.1:p.Ser431Thr
ENST00000646122.1:c.1409G>C	ENSP00000496222.1:p.Ser470Thr
ENST00000646196.1:n.2378G>C
ENST00000646223.1:c.*1402G>C	ENSP00000496043.1:n.*1402G>C
ENST00000646319.1:c.1409G>C	ENSP00000495377.1:p.Ser470Thr
ENST00000646390.1:n.3697G>C
ENST00000646627.1:c.851G>C	ENSP00000493795.1:p.Ser284Thr
ENST00000646679.1:c.851G>C	ENSP00000494887.1:p.Ser284Thr
ENST00000646822.1:n.2471G>C
ENST00000646940.1:n.1583G>C
ENST00000647286.1:n.1507G>C
ENST00000647477.1:n.148G>C
ENST00000399959.6:c.1409G>C	ENSP00000382840.2:p.Ser470Thr
ENST00000441189.3:c.341-1318G>C	ENSP00000414281.2:n.341-1318G>C
ENST00000457138.6:c.1361G>C	ENSP00000392494.2:p.Ser454Thr
ENST00000478993.5:c.1409G>C	ENSP00000478443.1:p.Ser470Thr
ENST00000542215.5:n.1457G>C
ENST00000625837.2:c.1409G>C	ENSP00000486306.1:p.Ser470Thr
ENST00000626301.2:c.1409G>C	ENSP00000486443.1:p.Ser470Thr
ENST00000629496.2:c.1409G>C	ENSP00000487224.1:p.Ser470Thr
ENST00000629785.2:c.1409G>C	ENSP00000486516.1:p.Ser470Thr
ENST00000630255.2:c.1409G>C	ENSP00000486720.1:p.Ser470Thr
ENST00000630370.2:c.1409G>C	ENSP00000487062.1:p.Ser470Thr
ENST00000630858.2:c.1409G>C	ENSP00000486514.1:p.Ser470Thr
NM_001193416.2:c.1409G>C	NP_001180345.1:p.Ser470Thr
NM_001193417.2:c.1361G>C	NP_001180346.1:p.Ser454Thr
NM_001356.4:c.1409G>C	NP_001347.3:p.Ser470Thr
NR_126093.1:n.2354G>C
XM_011543892.1:c.1409G>C	XP_011542194.1:p.Ser470Thr
NM_001363819.1:c.851G>C	NP_001350748.1:p.Ser284Thr
XM_011543892.2:c.1409G>C	XP_011542194.1:p.Ser470Thr
XM_017029313.1:c.851G>C	XP_016884802.1:p.Ser284Thr
NM_001193416.3:c.1409G>C	NP_001180345.1:p.Ser470Thr
NM_001193417.3:c.1361G>C	NP_001180346.1:p.Ser454Thr
NM_001356.5:c.1409G>C MANE Select	NP_001347.3:p.Ser470Thr