Canonical Allele Identifier: CA515972356
Gene: DDX3X HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.41205486G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346233G>A , CM000685.2:g.41346233G>A GRCh38
NC_000023.10:g.41205486G>A , CM000685.1:g.41205486G>A GRCh37
NC_000023.9:g.41090430G>A NCBI36
NG_012830.1:g.17836G>A
NG_012830.2:g.17836G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1452G>A ENSP00000496052.2:p.Lys484=
ENST00000399959.7:c.1317G>A ENSP00000382840.3:p.Lys439=
ENST00000441189.4:c.1221G>A ENSP00000414281.3:p.Lys407=
ENST00000457138.7:c.1272G>A ENSP00000392494.2:p.Lys424=
ENST00000616050.3:c.68G>A
ENST00000629496.3:c.1320G>A ENSP00000487224.1:p.Lys440=
ENST00000642161.1:n.3519G>A
ENST00000642322.1:c.762G>A ENSP00000496052.1:p.Lys254=
ENST00000642424.1:c.762G>A ENSP00000496356.1:p.Lys254=
ENST00000642589.1:n.4642G>A
ENST00000642597.1:n.1494G>A
ENST00000642687.1:n.1353G>A
ENST00000642722.1:n.2153G>A
ENST00000642763.1:n.2211G>A
ENST00000642793.1:c.*769G>A ENSP00000493976.1:n.*769G>A
ENST00000642801.1:n.969G>A
ENST00000643820.1:n.596G>A
ENST00000643963.1:c.*602G>A ENSP00000495264.1:n.*602G>A
ENST00000644073.1:c.1278G>A ENSP00000493475.1:p.Lys426=
ENST00000644074.1:c.1317G>A ENSP00000496663.1:p.Lys439=
ENST00000644109.1:c.1482G>A ENSP00000494952.1:p.Lys494=
ENST00000644307.1:n.1490G>A
ENST00000644513.1:c.1320G>A ENSP00000493819.1:p.Lys440=
ENST00000644677.1:c.1203G>A ENSP00000496524.1:p.Lys401=
ENST00000644876.2:c.1320G>A MANE Select ENSP00000494040.1:p.Lys440=
ENST00000644958.1:n.2981G>A
ENST00000645080.1:c.*2542G>A ENSP00000494767.1:n.*2542G>A
ENST00000645120.1:n.2815G>A
ENST00000645338.1:n.1490G>A
ENST00000645380.1:n.2784G>A
ENST00000645561.1:n.2496G>A
ENST00000645574.1:n.4184G>A
ENST00000645589.1:c.1320G>A ENSP00000494588.1:p.Lys440=
ENST00000646093.1:n.504G>A
ENST00000646107.1:c.1203G>A ENSP00000494518.1:p.Lys401=
ENST00000646122.1:c.1320G>A ENSP00000496222.1:p.Lys440=
ENST00000646196.1:n.2289G>A
ENST00000646223.1:c.*1313G>A ENSP00000496043.1:n.*1313G>A
ENST00000646319.1:c.1320G>A ENSP00000495377.1:p.Lys440=
ENST00000646390.1:n.3608G>A
ENST00000646627.1:c.762G>A ENSP00000493795.1:p.Lys254=
ENST00000646679.1:c.762G>A ENSP00000494887.1:p.Lys254=
ENST00000646822.1:n.2382G>A
ENST00000646940.1:n.1494G>A
ENST00000647286.1:n.1418G>A
ENST00000647477.1:n.59G>A
ENST00000399959.6:c.1320G>A ENSP00000382840.2:p.Lys440=
ENST00000441189.3:c.341-1407G>A ENSP00000414281.2:n.341-1407G>A
ENST00000457138.6:c.1272G>A ENSP00000392494.2:p.Lys424=
ENST00000478993.5:c.1320G>A ENSP00000478443.1:p.Lys440=
ENST00000542215.5:n.1368G>A
ENST00000625837.2:c.1320G>A ENSP00000486306.1:p.Lys440=
ENST00000626301.2:c.1320G>A ENSP00000486443.1:p.Lys440=
ENST00000629496.2:c.1320G>A ENSP00000487224.1:p.Lys440=
ENST00000629785.2:c.1320G>A ENSP00000486516.1:p.Lys440=
ENST00000630255.2:c.1320G>A ENSP00000486720.1:p.Lys440=
ENST00000630370.2:c.1320G>A ENSP00000487062.1:p.Lys440=
ENST00000630858.2:c.1320G>A ENSP00000486514.1:p.Lys440=
NM_001193416.2:c.1320G>A NP_001180345.1:p.Lys440=
NM_001193417.2:c.1272G>A NP_001180346.1:p.Lys424=
NM_001356.4:c.1320G>A NP_001347.3:p.Lys440=
NR_126093.1:n.2265G>A
XM_011543892.1:c.1320G>A XP_011542194.1:p.Lys440=
NM_001363819.1:c.762G>A NP_001350748.1:p.Lys254=
XM_011543892.2:c.1320G>A XP_011542194.1:p.Lys440=
XM_017029313.1:c.762G>A XP_016884802.1:p.Lys254=
NM_001193416.3:c.1320G>A NP_001180345.1:p.Lys440=
NM_001193417.3:c.1272G>A NP_001180346.1:p.Lys424=
NM_001356.5:c.1320G>A MANE Select NP_001347.3:p.Lys440=