Canonical Allele Identifier: CA515972445

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205573C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346320C>G , CM000685.2:g.41346320C>G	GRCh38
NC_000023.10:g.41205573C>G , CM000685.1:g.41205573C>G	GRCh37
NC_000023.9:g.41090517C>G	NCBI36
NG_012830.1:g.17923C>G
NG_012830.2:g.17923C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642322.2:c.1539C>G	ENSP00000496052.2:p.Thr513=
ENST00000399959.7:c.1404C>G	ENSP00000382840.3:p.Thr468=
ENST00000441189.4:c.1308C>G	ENSP00000414281.3:p.Thr436=
ENST00000457138.7:c.1359C>G	ENSP00000392494.2:p.Thr453=
ENST00000611968.2:c.1C>G
ENST00000616050.3:c.155C>G
ENST00000629496.3:c.1407C>G	ENSP00000487224.1:p.Thr469=
ENST00000642161.1:n.3606C>G
ENST00000642322.1:c.849C>G	ENSP00000496052.1:p.Thr283=
ENST00000642424.1:c.849C>G	ENSP00000496356.1:p.Thr283=
ENST00000642589.1:n.4729C>G
ENST00000642597.1:n.1581C>G
ENST00000642687.1:n.1440C>G
ENST00000642722.1:n.2240C>G
ENST00000642763.1:n.2298C>G
ENST00000642793.1:c.*856C>G	ENSP00000493976.1:n.*856C>G
ENST00000642801.1:n.1056C>G
ENST00000643820.1:n.683C>G
ENST00000643963.1:c.*689C>G	ENSP00000495264.1:n.*689C>G
ENST00000644073.1:c.1365C>G	ENSP00000493475.1:p.Thr455=
ENST00000644074.1:c.1404C>G	ENSP00000496663.1:p.Thr468=
ENST00000644109.1:c.1569C>G	ENSP00000494952.1:p.Thr523=
ENST00000644307.1:n.1577C>G
ENST00000644513.1:c.1407C>G	ENSP00000493819.1:p.Thr469=
ENST00000644677.1:c.1290C>G	ENSP00000496524.1:p.Thr430=
ENST00000644876.2:c.1407C>G MANE Select	ENSP00000494040.1:p.Thr469=
ENST00000644958.1:n.3068C>G
ENST00000645080.1:c.*2629C>G	ENSP00000494767.1:n.*2629C>G
ENST00000645120.1:n.2902C>G
ENST00000645338.1:n.1577C>G
ENST00000645380.1:n.2871C>G
ENST00000645561.1:n.2583C>G
ENST00000645574.1:n.4271C>G
ENST00000645589.1:c.1407C>G	ENSP00000494588.1:p.Thr469=
ENST00000646107.1:c.1290C>G	ENSP00000494518.1:p.Thr430=
ENST00000646122.1:c.1407C>G	ENSP00000496222.1:p.Thr469=
ENST00000646196.1:n.2376C>G
ENST00000646223.1:c.*1400C>G	ENSP00000496043.1:n.*1400C>G
ENST00000646319.1:c.1407C>G	ENSP00000495377.1:p.Thr469=
ENST00000646390.1:n.3695C>G
ENST00000646627.1:c.849C>G	ENSP00000493795.1:p.Thr283=
ENST00000646679.1:c.849C>G	ENSP00000494887.1:p.Thr283=
ENST00000646822.1:n.2469C>G
ENST00000646940.1:n.1581C>G
ENST00000647286.1:n.1505C>G
ENST00000647477.1:n.146C>G
ENST00000399959.6:c.1407C>G	ENSP00000382840.2:p.Thr469=
ENST00000441189.3:c.341-1320C>G	ENSP00000414281.2:n.341-1320C>G
ENST00000457138.6:c.1359C>G	ENSP00000392494.2:p.Thr453=
ENST00000478993.5:c.1407C>G	ENSP00000478443.1:p.Thr469=
ENST00000542215.5:n.1455C>G
ENST00000625837.2:c.1407C>G	ENSP00000486306.1:p.Thr469=
ENST00000626301.2:c.1407C>G	ENSP00000486443.1:p.Thr469=
ENST00000629496.2:c.1407C>G	ENSP00000487224.1:p.Thr469=
ENST00000629785.2:c.1407C>G	ENSP00000486516.1:p.Thr469=
ENST00000630255.2:c.1407C>G	ENSP00000486720.1:p.Thr469=
ENST00000630370.2:c.1407C>G	ENSP00000487062.1:p.Thr469=
ENST00000630858.2:c.1407C>G	ENSP00000486514.1:p.Thr469=
NM_001193416.2:c.1407C>G	NP_001180345.1:p.Thr469=
NM_001193417.2:c.1359C>G	NP_001180346.1:p.Thr453=
NM_001356.4:c.1407C>G	NP_001347.3:p.Thr469=
NR_126093.1:n.2352C>G
XM_011543892.1:c.1407C>G	XP_011542194.1:p.Thr469=
NM_001363819.1:c.849C>G	NP_001350748.1:p.Thr283=
XM_011543892.2:c.1407C>G	XP_011542194.1:p.Thr469=
XM_017029313.1:c.849C>G	XP_016884802.1:p.Thr283=
NM_001193416.3:c.1407C>G	NP_001180345.1:p.Thr469=
NM_001193417.3:c.1359C>G	NP_001180346.1:p.Thr453=
NM_001356.5:c.1407C>G MANE Select	NP_001347.3:p.Thr469=