Canonical Allele Identifier: CA10389642

Gene: DDX3X

Linked Data

• dbSNP Id: rs764294654
• ExAC: X:41205665 T / C
• MyVariant Identifiers: chrX:g.41205665T>C (hg19) ; chrX:g.41346412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346412T>C , CM000685.2:g.41346412T>C	GRCh38
NC_000023.10:g.41205665T>C , CM000685.1:g.41205665T>C	GRCh37
NC_000023.9:g.41090609T>C	NCBI36
NG_012830.1:g.18015T>C
NG_012830.2:g.18015T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1629+2T>C	ENSP00000496052.2:n.1629+2T>C
ENST00000399959.7:c.1494+2T>C	ENSP00000382840.3:n.1494+2T>C
ENST00000441189.4:c.1398+2T>C	ENSP00000414281.3:n.1398+2T>C
ENST00000457138.7:c.1449+2T>C	ENSP00000392494.2:n.1449+2T>C
ENST00000611968.2:c.91+2T>C
ENST00000616050.3:c.245+2T>C
ENST00000629496.3:c.1497+2T>C	ENSP00000487224.1:n.1497+2T>C
ENST00000642161.1:n.3696+2T>C
ENST00000642322.1:c.939+2T>C	ENSP00000496052.1:n.939+2T>C
ENST00000642424.1:c.939+2T>C	ENSP00000496356.1:n.939+2T>C
ENST00000642589.1:n.4819+2T>C
ENST00000642597.1:n.1671+2T>C
ENST00000642687.1:n.1530+2T>C
ENST00000642722.1:n.2330+2T>C
ENST00000642763.1:n.2388+2T>C
ENST00000642793.1:c.*946+2T>C	ENSP00000493976.1:n.*946+2T>C
ENST00000642801.1:n.1146+2T>C
ENST00000643820.1:n.775T>C
ENST00000643963.1:c.*779+2T>C	ENSP00000495264.1:n.*779+2T>C
ENST00000644073.1:c.1455+2T>C	ENSP00000493475.1:n.1455+2T>C
ENST00000644074.1:c.1494+2T>C	ENSP00000496663.1:n.1494+2T>C
ENST00000644109.1:c.1659+2T>C	ENSP00000494952.1:n.1659+2T>C
ENST00000644307.1:n.1667+2T>C
ENST00000644513.1:c.1497+2T>C	ENSP00000493819.1:n.1497+2T>C
ENST00000644677.1:c.1380+2T>C	ENSP00000496524.1:n.1380+2T>C
ENST00000644876.2:c.1497+2T>C MANE Select	ENSP00000494040.1:n.1497+2T>C
ENST00000644958.1:n.3158+2T>C
ENST00000645080.1:c.*2719+2T>C	ENSP00000494767.1:n.*2719+2T>C
ENST00000645120.1:n.2992+2T>C
ENST00000645338.1:n.1667+2T>C
ENST00000645380.1:n.2961+2T>C
ENST00000645561.1:n.2673+2T>C
ENST00000645574.1:n.4361+2T>C
ENST00000645589.1:c.1497+2T>C	ENSP00000494588.1:n.1497+2T>C
ENST00000646107.1:c.1380+2T>C	ENSP00000494518.1:n.1380+2T>C
ENST00000646122.1:c.1497+2T>C	ENSP00000496222.1:n.1497+2T>C
ENST00000646196.1:n.2466+2T>C
ENST00000646223.1:c.*1490+2T>C	ENSP00000496043.1:n.*1490+2T>C
ENST00000646319.1:c.1497+2T>C	ENSP00000495377.1:n.1497+2T>C
ENST00000646390.1:n.3785+2T>C
ENST00000646627.1:c.939+2T>C	ENSP00000493795.1:n.939+2T>C
ENST00000646679.1:c.939+2T>C	ENSP00000494887.1:n.939+2T>C
ENST00000646822.1:n.2559+2T>C
ENST00000646940.1:n.1671+2T>C
ENST00000647286.1:n.1595+2T>C
ENST00000647477.1:n.236+2T>C
ENST00000399959.6:c.1497+2T>C	ENSP00000382840.2:n.1497+2T>C
ENST00000441189.3:c.341-1228T>C	ENSP00000414281.2:n.341-1228T>C
ENST00000457138.6:c.1449+2T>C	ENSP00000392494.2:n.1449+2T>C
ENST00000478993.5:c.1497+2T>C	ENSP00000478443.1:n.1497+2T>C
ENST00000542215.5:n.1545+2T>C
ENST00000616050.2:c.50+2T>C
ENST00000625837.2:c.1497+2T>C	ENSP00000486306.1:n.1497+2T>C
ENST00000626301.2:c.1497+2T>C	ENSP00000486443.1:n.1497+2T>C
ENST00000629496.2:c.1497+2T>C	ENSP00000487224.1:n.1497+2T>C
ENST00000629785.2:c.1497+2T>C	ENSP00000486516.1:n.1497+2T>C
ENST00000630255.2:c.1497+2T>C	ENSP00000486720.1:n.1497+2T>C
ENST00000630370.2:c.1497+2T>C	ENSP00000487062.1:n.1497+2T>C
ENST00000630858.2:c.1497+2T>C	ENSP00000486514.1:n.1497+2T>C
NM_001193416.2:c.1497+2T>C	NP_001180345.1:n.1497+2T>C
NM_001193417.2:c.1449+2T>C	NP_001180346.1:n.1449+2T>C
NM_001356.4:c.1497+2T>C	NP_001347.3:n.1497+2T>C
NR_126093.1:n.2442+2T>C
XM_011543892.1:c.1497+2T>C	XP_011542194.1:n.1497+2T>C
NM_001363819.1:c.939+2T>C	NP_001350748.1:n.939+2T>C
XM_011543892.2:c.1497+2T>C	XP_011542194.1:n.1497+2T>C
XM_017029313.1:c.939+2T>C	XP_016884802.1:n.939+2T>C
NM_001193416.3:c.1497+2T>C	NP_001180345.1:n.1497+2T>C
NM_001193417.3:c.1449+2T>C	NP_001180346.1:n.1449+2T>C
NM_001356.5:c.1497+2T>C MANE Select	NP_001347.3:n.1497+2T>C