Canonical Allele Identifier: CA412771486

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204546T>G (hg19) ; chrX:g.41345293T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345293T>G , CM000685.2:g.41345293T>G	GRCh38
NC_000023.10:g.41204546T>G , CM000685.1:g.41204546T>G	GRCh37
NC_000023.9:g.41089490T>G	NCBI36
NG_012830.1:g.16896T>G
NG_012830.2:g.16896T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1271T>G	ENSP00000496052.2:p.Met424Arg
ENST00000399959.7:c.1136T>G	ENSP00000382840.3:p.Met379Arg
ENST00000441189.4:c.1040T>G	ENSP00000414281.3:p.Met347Arg
ENST00000457138.7:c.1091T>G	ENSP00000392494.2:p.Met364Arg
ENST00000629496.3:c.1139T>G	ENSP00000487224.1:p.Met380Arg
ENST00000642161.1:n.3338T>G
ENST00000642322.1:c.581T>G	ENSP00000496052.1:p.Met194Arg
ENST00000642424.1:c.581T>G	ENSP00000496356.1:p.Met194Arg
ENST00000642589.1:n.4461T>G
ENST00000642597.1:n.1313T>G
ENST00000642687.1:n.1172T>G
ENST00000642722.1:n.1972T>G
ENST00000642763.1:n.2030T>G
ENST00000642793.1:c.*588T>G	ENSP00000493976.1:n.*588T>G
ENST00000642801.1:n.788T>G
ENST00000643820.1:n.415T>G
ENST00000643963.1:c.*421T>G	ENSP00000495264.1:n.*421T>G
ENST00000644073.1:c.1097T>G	ENSP00000493475.1:p.Met366Arg
ENST00000644074.1:c.1136T>G	ENSP00000496663.1:p.Met379Arg
ENST00000644109.1:c.1301T>G	ENSP00000494952.1:p.Met434Arg
ENST00000644307.1:n.1230T>G
ENST00000644513.1:c.1139T>G	ENSP00000493819.1:p.Met380Arg
ENST00000644677.1:c.1022T>G	ENSP00000496524.1:p.Met341Arg
ENST00000644876.2:c.1139T>G MANE Select	ENSP00000494040.1:p.Met380Arg
ENST00000644958.1:n.2800T>G
ENST00000645080.1:c.*2361T>G	ENSP00000494767.1:n.*2361T>G
ENST00000645120.1:n.2634T>G
ENST00000645338.1:n.1230T>G
ENST00000645380.1:n.2524T>G
ENST00000645561.1:n.2315T>G
ENST00000645574.1:n.4003T>G
ENST00000645589.1:c.1139T>G	ENSP00000494588.1:p.Met380Arg
ENST00000646093.1:n.323T>G
ENST00000646107.1:c.1022T>G	ENSP00000494518.1:p.Met341Arg
ENST00000646122.1:c.1139T>G	ENSP00000496222.1:p.Met380Arg
ENST00000646196.1:n.2108T>G
ENST00000646223.1:c.*1132T>G	ENSP00000496043.1:n.*1132T>G
ENST00000646319.1:c.1139T>G	ENSP00000495377.1:p.Met380Arg
ENST00000646390.1:n.3427T>G
ENST00000646627.1:c.581T>G	ENSP00000493795.1:p.Met194Arg
ENST00000646679.1:c.581T>G	ENSP00000494887.1:p.Met194Arg
ENST00000646822.1:n.2201T>G
ENST00000646940.1:n.1313T>G
ENST00000647286.1:n.1237T>G
ENST00000399959.6:c.1139T>G	ENSP00000382840.2:p.Met380Arg
ENST00000441189.3:c.341-2347T>G	ENSP00000414281.2:n.341-2347T>G
ENST00000457138.6:c.1091T>G	ENSP00000392494.2:p.Met364Arg
ENST00000478993.5:c.1139T>G	ENSP00000478443.1:p.Met380Arg
ENST00000542215.5:n.1187T>G
ENST00000625837.2:c.1139T>G	ENSP00000486306.1:p.Met380Arg
ENST00000626301.2:c.1139T>G	ENSP00000486443.1:p.Met380Arg
ENST00000629496.2:c.1139T>G	ENSP00000487224.1:p.Met380Arg
ENST00000629785.2:c.1139T>G	ENSP00000486516.1:p.Met380Arg
ENST00000630255.2:c.1139T>G	ENSP00000486720.1:p.Met380Arg
ENST00000630370.2:c.1139T>G	ENSP00000487062.1:p.Met380Arg
ENST00000630858.2:c.1139T>G	ENSP00000486514.1:p.Met380Arg
NM_001193416.2:c.1139T>G	NP_001180345.1:p.Met380Arg
NM_001193417.2:c.1091T>G	NP_001180346.1:p.Met364Arg
NM_001356.4:c.1139T>G	NP_001347.3:p.Met380Arg
NR_126093.1:n.2084T>G
XM_011543892.1:c.1139T>G	XP_011542194.1:p.Met380Arg
NM_001363819.1:c.581T>G	NP_001350748.1:p.Met194Arg
XM_011543892.2:c.1139T>G	XP_011542194.1:p.Met380Arg
XM_017029313.1:c.581T>G	XP_016884802.1:p.Met194Arg
NM_001193416.3:c.1139T>G	NP_001180345.1:p.Met380Arg
NM_001193417.3:c.1091T>G	NP_001180346.1:p.Met364Arg
NM_001356.5:c.1139T>G MANE Select	NP_001347.3:p.Met380Arg