Canonical Allele Identifier: CA412777021

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205867G>C (hg19) ; chrX:g.41346614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346614G>C , CM000685.2:g.41346614G>C	GRCh38
NC_000023.10:g.41205867G>C , CM000685.1:g.41205867G>C	GRCh37
NC_000023.9:g.41090811G>C	NCBI36
NG_012830.1:g.18217G>C
NG_012830.2:g.18217G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1739G>C	ENSP00000496052.2:p.Gly580Ala
ENST00000399959.7:c.1604G>C	ENSP00000382840.3:p.Gly535Ala
ENST00000441189.4:c.1508G>C	ENSP00000414281.3:p.Gly503Ala
ENST00000457138.7:c.1559G>C	ENSP00000392494.2:p.Gly520Ala
ENST00000611968.2:c.201G>C
ENST00000616050.3:c.355G>C
ENST00000629496.3:c.1607G>C	ENSP00000487224.1:p.Gly536Ala
ENST00000642161.1:n.3806G>C
ENST00000642322.1:c.1049G>C	ENSP00000496052.1:p.Gly350Ala
ENST00000642424.1:c.1049G>C	ENSP00000496356.1:p.Gly350Ala
ENST00000642589.1:n.4929G>C
ENST00000642597.1:n.1781G>C
ENST00000642687.1:n.1640G>C
ENST00000642722.1:n.2440G>C
ENST00000642763.1:n.2498G>C
ENST00000642793.1:c.*1056G>C	ENSP00000493976.1:n.*1056G>C
ENST00000642801.1:n.1256G>C
ENST00000643820.1:n.977G>C
ENST00000643963.1:c.*889G>C	ENSP00000495264.1:n.*889G>C
ENST00000644073.1:c.1565G>C	ENSP00000493475.1:p.Gly522Ala
ENST00000644074.1:c.1604G>C	ENSP00000496663.1:p.Gly535Ala
ENST00000644109.1:c.1769G>C	ENSP00000494952.1:p.Gly590Ala
ENST00000644307.1:n.1777G>C
ENST00000644513.1:c.1607G>C	ENSP00000493819.1:p.Gly536Ala
ENST00000644677.1:c.1490G>C	ENSP00000496524.1:p.Gly497Ala
ENST00000644876.2:c.1607G>C MANE Select	ENSP00000494040.1:p.Gly536Ala
ENST00000644958.1:n.3268G>C
ENST00000645080.1:c.*2829G>C	ENSP00000494767.1:n.*2829G>C
ENST00000645120.1:n.3102G>C
ENST00000645338.1:n.1777G>C
ENST00000645380.1:n.3071G>C
ENST00000645561.1:n.2783G>C
ENST00000645574.1:n.4471G>C
ENST00000645589.1:c.*106G>C	ENSP00000494588.1:n.*106G>C
ENST00000646107.1:c.1490G>C	ENSP00000494518.1:p.Gly497Ala
ENST00000646122.1:c.1607G>C	ENSP00000496222.1:p.Gly536Ala
ENST00000646196.1:n.2576G>C
ENST00000646223.1:c.*1600G>C	ENSP00000496043.1:n.*1600G>C
ENST00000646319.1:c.1607G>C	ENSP00000495377.1:p.Gly536Ala
ENST00000646390.1:n.3895G>C
ENST00000646627.1:c.1049G>C	ENSP00000493795.1:p.Gly350Ala
ENST00000646679.1:c.1049G>C	ENSP00000494887.1:p.Gly350Ala
ENST00000646822.1:n.2669G>C
ENST00000646940.1:n.1781G>C
ENST00000647286.1:n.1705G>C
ENST00000647477.1:n.346G>C
ENST00000399959.6:c.1607G>C	ENSP00000382840.2:p.Gly536Ala
ENST00000441189.3:c.341-1026G>C	ENSP00000414281.2:n.341-1026G>C
ENST00000457138.6:c.1559G>C	ENSP00000392494.2:p.Gly520Ala
ENST00000478993.5:c.1607G>C	ENSP00000478443.1:p.Gly536Ala
ENST00000611968.1:c.49G>C
ENST00000616050.2:c.160G>C
ENST00000625837.2:c.1607G>C	ENSP00000486306.1:p.Gly536Ala
ENST00000626301.2:c.1607G>C	ENSP00000486443.1:p.Gly536Ala
ENST00000629496.2:c.1607G>C	ENSP00000487224.1:p.Gly536Ala
ENST00000629785.2:c.1607G>C	ENSP00000486516.1:p.Gly536Ala
ENST00000630255.2:c.1607G>C	ENSP00000486720.1:p.Gly536Ala
ENST00000630370.2:c.1607G>C	ENSP00000487062.1:p.Gly536Ala
ENST00000630858.2:c.1607G>C	ENSP00000486514.1:p.Gly536Ala
NM_001193416.2:c.1607G>C	NP_001180345.1:p.Gly536Ala
NM_001193417.2:c.1559G>C	NP_001180346.1:p.Gly520Ala
NM_001356.4:c.1607G>C	NP_001347.3:p.Gly536Ala
NR_126093.1:n.2552G>C
XM_011543892.1:c.1607G>C	XP_011542194.1:p.Gly536Ala
NM_001363819.1:c.1049G>C	NP_001350748.1:p.Gly350Ala
XM_011543892.2:c.1607G>C	XP_011542194.1:p.Gly536Ala
XM_017029313.1:c.1049G>C	XP_016884802.1:p.Gly350Ala
NM_001193416.3:c.1607G>C	NP_001180345.1:p.Gly536Ala
NM_001193417.3:c.1559G>C	NP_001180346.1:p.Gly520Ala
NM_001356.5:c.1607G>C MANE Select	NP_001347.3:p.Gly536Ala