Canonical Allele Identifier: CA515972398

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41205537G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346284G>C , CM000685.2:g.41346284G>C	GRCh38
NC_000023.10:g.41205537G>C , CM000685.1:g.41205537G>C	GRCh37
NC_000023.9:g.41090481G>C	NCBI36
NG_012830.1:g.17887G>C
NG_012830.2:g.17887G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1503G>C	ENSP00000496052.2:p.Leu501=
ENST00000399959.7:c.1368G>C	ENSP00000382840.3:p.Leu456=
ENST00000441189.4:c.1272G>C	ENSP00000414281.3:p.Leu424=
ENST00000457138.7:c.1323G>C	ENSP00000392494.2:p.Leu441=
ENST00000616050.3:c.119G>C
ENST00000629496.3:c.1371G>C	ENSP00000487224.1:p.Leu457=
ENST00000642161.1:n.3570G>C
ENST00000642322.1:c.813G>C	ENSP00000496052.1:p.Leu271=
ENST00000642424.1:c.813G>C	ENSP00000496356.1:p.Leu271=
ENST00000642589.1:n.4693G>C
ENST00000642597.1:n.1545G>C
ENST00000642687.1:n.1404G>C
ENST00000642722.1:n.2204G>C
ENST00000642763.1:n.2262G>C
ENST00000642793.1:c.*820G>C	ENSP00000493976.1:n.*820G>C
ENST00000642801.1:n.1020G>C
ENST00000643820.1:n.647G>C
ENST00000643963.1:c.*653G>C	ENSP00000495264.1:n.*653G>C
ENST00000644073.1:c.1329G>C	ENSP00000493475.1:p.Leu443=
ENST00000644074.1:c.1368G>C	ENSP00000496663.1:p.Leu456=
ENST00000644109.1:c.1533G>C	ENSP00000494952.1:p.Leu511=
ENST00000644307.1:n.1541G>C
ENST00000644513.1:c.1371G>C	ENSP00000493819.1:p.Leu457=
ENST00000644677.1:c.1254G>C	ENSP00000496524.1:p.Leu418=
ENST00000644876.2:c.1371G>C MANE Select	ENSP00000494040.1:p.Leu457=
ENST00000644958.1:n.3032G>C
ENST00000645080.1:c.*2593G>C	ENSP00000494767.1:n.*2593G>C
ENST00000645120.1:n.2866G>C
ENST00000645338.1:n.1541G>C
ENST00000645380.1:n.2835G>C
ENST00000645561.1:n.2547G>C
ENST00000645574.1:n.4235G>C
ENST00000645589.1:c.1371G>C	ENSP00000494588.1:p.Leu457=
ENST00000646107.1:c.1254G>C	ENSP00000494518.1:p.Leu418=
ENST00000646122.1:c.1371G>C	ENSP00000496222.1:p.Leu457=
ENST00000646196.1:n.2340G>C
ENST00000646223.1:c.*1364G>C	ENSP00000496043.1:n.*1364G>C
ENST00000646319.1:c.1371G>C	ENSP00000495377.1:p.Leu457=
ENST00000646390.1:n.3659G>C
ENST00000646627.1:c.813G>C	ENSP00000493795.1:p.Leu271=
ENST00000646679.1:c.813G>C	ENSP00000494887.1:p.Leu271=
ENST00000646822.1:n.2433G>C
ENST00000646940.1:n.1545G>C
ENST00000647286.1:n.1469G>C
ENST00000647477.1:n.110G>C
ENST00000399959.6:c.1371G>C	ENSP00000382840.2:p.Leu457=
ENST00000441189.3:c.341-1356G>C	ENSP00000414281.2:n.341-1356G>C
ENST00000457138.6:c.1323G>C	ENSP00000392494.2:p.Leu441=
ENST00000478993.5:c.1371G>C	ENSP00000478443.1:p.Leu457=
ENST00000542215.5:n.1419G>C
ENST00000625837.2:c.1371G>C	ENSP00000486306.1:p.Leu457=
ENST00000626301.2:c.1371G>C	ENSP00000486443.1:p.Leu457=
ENST00000629496.2:c.1371G>C	ENSP00000487224.1:p.Leu457=
ENST00000629785.2:c.1371G>C	ENSP00000486516.1:p.Leu457=
ENST00000630255.2:c.1371G>C	ENSP00000486720.1:p.Leu457=
ENST00000630370.2:c.1371G>C	ENSP00000487062.1:p.Leu457=
ENST00000630858.2:c.1371G>C	ENSP00000486514.1:p.Leu457=
NM_001193416.2:c.1371G>C	NP_001180345.1:p.Leu457=
NM_001193417.2:c.1323G>C	NP_001180346.1:p.Leu441=
NM_001356.4:c.1371G>C	NP_001347.3:p.Leu457=
NR_126093.1:n.2316G>C
XM_011543892.1:c.1371G>C	XP_011542194.1:p.Leu457=
NM_001363819.1:c.813G>C	NP_001350748.1:p.Leu271=
XM_011543892.2:c.1371G>C	XP_011542194.1:p.Leu457=
XM_017029313.1:c.813G>C	XP_016884802.1:p.Leu271=
NM_001193416.3:c.1371G>C	NP_001180345.1:p.Leu457=
NM_001193417.3:c.1323G>C	NP_001180346.1:p.Leu441=
NM_001356.5:c.1371G>C MANE Select	NP_001347.3:p.Leu457=