Canonical Allele Identifier: CA2820566933
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346535dup , CM000685.2:g.41346535dup GRCh38
NC_000023.10:g.41205788dup , CM000685.1:g.41205788dup GRCh37
NC_000023.9:g.41090732dup NCBI36
NG_012830.1:g.18138dup
NG_012830.2:g.18138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1660dup ENSP00000496052.2:p.Val554GlyfsTer8
ENST00000399959.7:c.1525dup ENSP00000382840.3:p.Val509GlyfsTer8
ENST00000441189.4:c.1429dup ENSP00000414281.3:p.Val477GlyfsTer8
ENST00000457138.7:c.1480dup ENSP00000392494.2:p.Val494GlyfsTer8
ENST00000611968.2:c.122dup
ENST00000616050.3:c.276dup
ENST00000629496.3:c.1528dup ENSP00000487224.1:p.Val510GlyfsTer8
ENST00000642161.1:n.3727dup
ENST00000642322.1:c.970dup ENSP00000496052.1:p.Val324GlyfsTer8
ENST00000642424.1:c.970dup ENSP00000496356.1:p.Val324GlyfsTer8
ENST00000642589.1:n.4850dup
ENST00000642597.1:n.1702dup
ENST00000642687.1:n.1561dup
ENST00000642722.1:n.2361dup
ENST00000642763.1:n.2419dup
ENST00000642793.1:c.*977dup ENSP00000493976.1:n.*977dup
ENST00000642801.1:n.1177dup
ENST00000643820.1:n.898dup
ENST00000643963.1:c.*810dup ENSP00000495264.1:n.*810dup
ENST00000644073.1:c.1486dup ENSP00000493475.1:p.Val496GlyfsTer8
ENST00000644074.1:c.1525dup ENSP00000496663.1:p.Val509GlyfsTer8
ENST00000644109.1:c.1690dup ENSP00000494952.1:p.Val564GlyfsTer8
ENST00000644307.1:n.1698dup
ENST00000644513.1:c.1528dup ENSP00000493819.1:p.Val510GlyfsTer8
ENST00000644677.1:c.1411dup ENSP00000496524.1:p.Val471GlyfsTer8
ENST00000644876.2:c.1528dup MANE Select ENSP00000494040.1:p.Val510GlyfsTer8
ENST00000644958.1:n.3189dup
ENST00000645080.1:c.*2750dup ENSP00000494767.1:n.*2750dup
ENST00000645120.1:n.3023dup
ENST00000645338.1:n.1698dup
ENST00000645380.1:n.2992dup
ENST00000645561.1:n.2704dup
ENST00000645574.1:n.4392dup
ENST00000645589.1:c.*27dup ENSP00000494588.1:n.*27dup
ENST00000646107.1:c.1411dup ENSP00000494518.1:p.Val471GlyfsTer8
ENST00000646122.1:c.1528dup ENSP00000496222.1:p.Val510GlyfsTer8
ENST00000646196.1:n.2497dup
ENST00000646223.1:c.*1521dup ENSP00000496043.1:n.*1521dup
ENST00000646319.1:c.1528dup ENSP00000495377.1:p.Val510GlyfsTer8
ENST00000646390.1:n.3816dup
ENST00000646627.1:c.970dup ENSP00000493795.1:p.Val324GlyfsTer8
ENST00000646679.1:c.970dup ENSP00000494887.1:p.Val324GlyfsTer8
ENST00000646822.1:n.2590dup
ENST00000646940.1:n.1702dup
ENST00000647286.1:n.1626dup
ENST00000647477.1:n.267dup
ENST00000399959.6:c.1528dup ENSP00000382840.2:p.Val510GlyfsTer8
ENST00000441189.3:c.341-1105dup ENSP00000414281.2:n.341-1105dup
ENST00000457138.6:c.1480dup ENSP00000392494.2:p.Val494GlyfsTer8
ENST00000478993.5:c.1528dup ENSP00000478443.1:p.Val510GlyfsTer8
ENST00000542215.5:n.1576dup
ENST00000616050.2:c.81dup
ENST00000625837.2:c.1528dup ENSP00000486306.1:p.Val510GlyfsTer8
ENST00000626301.2:c.1528dup ENSP00000486443.1:p.Val510GlyfsTer8
ENST00000629496.2:c.1528dup ENSP00000487224.1:p.Val510GlyfsTer8
ENST00000629785.2:c.1528dup ENSP00000486516.1:p.Val510GlyfsTer8
ENST00000630255.2:c.1528dup ENSP00000486720.1:p.Val510GlyfsTer8
ENST00000630370.2:c.1528dup ENSP00000487062.1:p.Val510GlyfsTer8
ENST00000630858.2:c.1528dup ENSP00000486514.1:p.Val510GlyfsTer8
NM_001193416.2:c.1528dup NP_001180345.1:p.Val510GlyfsTer8
NM_001193417.2:c.1480dup NP_001180346.1:p.Val494GlyfsTer8
NM_001356.4:c.1528dup NP_001347.3:p.Val510GlyfsTer8
NR_126093.1:n.2473dup
XM_011543892.1:c.1528dup XP_011542194.1:p.Val510GlyfsTer8
NM_001363819.1:c.970dup NP_001350748.1:p.Val324GlyfsTer8
XM_011543892.2:c.1528dup XP_011542194.1:p.Val510GlyfsTer8
XM_017029313.1:c.970dup XP_016884802.1:p.Val324GlyfsTer8
NM_001193416.3:c.1528dup NP_001180345.1:p.Val510GlyfsTer8
NM_001193417.3:c.1480dup NP_001180346.1:p.Val494GlyfsTer8
NM_001356.5:c.1528dup MANE Select NP_001347.3:p.Val510GlyfsTer8