Canonical Allele Identifier: CA2425880928

Gene: DDX3X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345010T= , CM000685.2:g.41345010T=	GRCh38
NC_000023.10:g.41204263T= , CM000685.1:g.41204263T=	GRCh37
NC_000023.9:g.41089207T=	NCBI36
NG_012830.1:g.16613T=
NG_012830.2:g.16613T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1158-170T=	ENSP00000496052.2:n.1158-170T=
ENST00000399959.7:c.1023-170T=	ENSP00000382840.3:n.1023-170T=
ENST00000441189.4:c.927-170T=	ENSP00000414281.3:n.927-170T=
ENST00000457138.7:c.978-170T=	ENSP00000392494.2:n.978-170T=
ENST00000629496.3:c.1026-170T=	ENSP00000487224.1:n.1026-170T=
ENST00000642161.1:n.3225-170T=
ENST00000642322.1:c.468-170T=	ENSP00000496052.1:n.468-170T=
ENST00000642424.1:c.468-170T=	ENSP00000496356.1:n.468-170T=
ENST00000642589.1:n.4348-170T=
ENST00000642597.1:n.1200-170T=
ENST00000642687.1:n.1059-170T=
ENST00000642722.1:n.1859-170T=
ENST00000642763.1:n.1917-170T=
ENST00000642793.1:c.*475-170T=	ENSP00000493976.1:n.*475-170T=
ENST00000642801.1:n.675-170T=
ENST00000643820.1:n.302-170T=
ENST00000643963.1:c.*308-170T=	ENSP00000495264.1:n.*308-170T=
ENST00000644073.1:c.984-170T=	ENSP00000493475.1:n.984-170T=
ENST00000644074.1:c.1023-170T=	ENSP00000496663.1:n.1023-170T=
ENST00000644109.1:c.1188-170T=	ENSP00000494952.1:n.1188-170T=
ENST00000644307.1:n.1117-170T=
ENST00000644513.1:c.1026-170T=	ENSP00000493819.1:n.1026-170T=
ENST00000644677.1:c.909-170T=	ENSP00000496524.1:n.909-170T=
ENST00000644876.2:c.1026-170T= MANE Select	ENSP00000494040.1:n.1026-170T=
ENST00000644958.1:n.2687-170T=
ENST00000645080.1:c.*2248-170T=	ENSP00000494767.1:n.*2248-170T=
ENST00000645120.1:n.2521-170T=
ENST00000645338.1:n.1117-170T=
ENST00000645380.1:n.2411-170T=
ENST00000645561.1:n.2202-170T=
ENST00000645574.1:n.3890-170T=
ENST00000645589.1:c.1026-170T=	ENSP00000494588.1:n.1026-170T=
ENST00000646093.1:n.210-170T=
ENST00000646107.1:c.909-170T=	ENSP00000494518.1:n.909-170T=
ENST00000646122.1:c.1026-170T=	ENSP00000496222.1:n.1026-170T=
ENST00000646196.1:n.1995-170T=
ENST00000646223.1:c.*1019-170T=	ENSP00000496043.1:n.*1019-170T=
ENST00000646319.1:c.1026-170T=	ENSP00000495377.1:n.1026-170T=
ENST00000646390.1:n.3314-170T=
ENST00000646627.1:c.468-170T=	ENSP00000493795.1:n.468-170T=
ENST00000646679.1:c.468-170T=	ENSP00000494887.1:n.468-170T=
ENST00000646822.1:n.2088-170T=
ENST00000646940.1:n.1200-170T=
ENST00000647286.1:n.1124-170T=
ENST00000399959.6:c.1026-170T=	ENSP00000382840.2:n.1026-170T=
ENST00000441189.3:c.340+2460T=	ENSP00000414281.2:n.340+2460T=
ENST00000457138.6:c.978-170T=	ENSP00000392494.2:n.978-170T=
ENST00000478993.5:c.1026-170T=	ENSP00000478443.1:n.1026-170T=
ENST00000542215.5:n.1074-170T=
ENST00000625837.2:c.1026-170T=	ENSP00000486306.1:n.1026-170T=
ENST00000626301.2:c.1026-170T=	ENSP00000486443.1:n.1026-170T=
ENST00000629496.2:c.1026-170T=	ENSP00000487224.1:n.1026-170T=
ENST00000629785.2:c.1026-170T=	ENSP00000486516.1:n.1026-170T=
ENST00000630255.2:c.1026-170T=	ENSP00000486720.1:n.1026-170T=
ENST00000630370.2:c.1026-170T=	ENSP00000487062.1:n.1026-170T=
ENST00000630858.2:c.1026-170T=	ENSP00000486514.1:n.1026-170T=
NM_001193416.2:c.1026-170T=	NP_001180345.1:n.1026-170T=
NM_001193417.2:c.978-170T=	NP_001180346.1:n.978-170T=
NM_001356.4:c.1026-170T=	NP_001347.3:n.1026-170T=
NR_126093.1:n.1971-170T=
XM_011543892.1:c.1026-170T=	XP_011542194.1:n.1026-170T=
NM_001363819.1:c.468-170T=	NP_001350748.1:n.468-170T=
XM_011543892.2:c.1026-170T=	XP_011542194.1:n.1026-170T=
XM_017029313.1:c.468-170T=	XP_016884802.1:n.468-170T=
NM_001193416.3:c.1026-170T=	NP_001180345.1:n.1026-170T=
NM_001193417.3:c.978-170T=	NP_001180346.1:n.978-170T=
NM_001356.5:c.1026-170T= MANE Select	NP_001347.3:n.1026-170T=