Canonical Allele Identifier: CA2425881490
Gene: DDX3X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41346541_41346543delinsCAT , CM000685.2:g.41346541_41346543delinsCAT GRCh38
NC_000023.10:g.41205794_41205796delinsCAT , CM000685.1:g.41205794_41205796delinsCAT GRCh37
NC_000023.9:g.41090738_41090740delinsCAT NCBI36
NG_012830.1:g.18144_18146delinsCAT
NG_012830.2:g.18144_18146delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000642322.2:c.1666_1668delinsCAT ENSP00000496052.2:p.His556=
ENST00000399959.7:c.1531_1533delinsCAT ENSP00000382840.3:p.His511=
ENST00000441189.4:c.1435_1437delinsCAT ENSP00000414281.3:p.His479=
ENST00000457138.7:c.1486_1488delinsCAT ENSP00000392494.2:p.His496=
ENST00000611968.2:c.128_130delinsCAT
ENST00000616050.3:c.282_284delinsCAT
ENST00000629496.3:c.1534_1536delinsCAT ENSP00000487224.1:p.His512=
ENST00000642161.1:n.3733_3735delinsCAT
ENST00000642322.1:c.976_978delinsCAT ENSP00000496052.1:p.His326=
ENST00000642424.1:c.976_978delinsCAT ENSP00000496356.1:p.His326=
ENST00000642589.1:n.4856_4858delinsCAT
ENST00000642597.1:n.1708_1710delinsCAT
ENST00000642687.1:n.1567_1569delinsCAT
ENST00000642722.1:n.2367_2369delinsCAT
ENST00000642763.1:n.2425_2427delinsCAT
ENST00000642793.1:c.*983_*985delinsCAT ENSP00000493976.1:n.*983_*985delinsCAT
ENST00000642801.1:n.1183_1185delinsCAT
ENST00000643820.1:n.904_906delinsCAT
ENST00000643963.1:c.*816_*818delinsCAT ENSP00000495264.1:n.*816_*818delinsCAT
ENST00000644073.1:c.1492_1494delinsCAT ENSP00000493475.1:p.His498=
ENST00000644074.1:c.1531_1533delinsCAT ENSP00000496663.1:p.His511=
ENST00000644109.1:c.1696_1698delinsCAT ENSP00000494952.1:p.His566=
ENST00000644307.1:n.1704_1706delinsCAT
ENST00000644513.1:c.1534_1536delinsCAT ENSP00000493819.1:p.His512=
ENST00000644677.1:c.1417_1419delinsCAT ENSP00000496524.1:p.His473=
ENST00000644876.2:c.1534_1536delinsCAT MANE Select ENSP00000494040.1:p.His512=
ENST00000644958.1:n.3195_3197delinsCAT
ENST00000645080.1:c.*2756_*2758delinsCAT ENSP00000494767.1:n.*2756_*2758delinsCAT
ENST00000645120.1:n.3029_3031delinsCAT
ENST00000645338.1:n.1704_1706delinsCAT
ENST00000645380.1:n.2998_3000delinsCAT
ENST00000645561.1:n.2710_2712delinsCAT
ENST00000645574.1:n.4398_4400delinsCAT
ENST00000645589.1:c.*33_*35delinsCAT ENSP00000494588.1:n.*33_*35delinsCAT
ENST00000646107.1:c.1417_1419delinsCAT ENSP00000494518.1:p.His473=
ENST00000646122.1:c.1534_1536delinsCAT ENSP00000496222.1:p.His512=
ENST00000646196.1:n.2503_2505delinsCAT
ENST00000646223.1:c.*1527_*1529delinsCAT ENSP00000496043.1:n.*1527_*1529delinsCAT
ENST00000646319.1:c.1534_1536delinsCAT ENSP00000495377.1:p.His512=
ENST00000646390.1:n.3822_3824delinsCAT
ENST00000646627.1:c.976_978delinsCAT ENSP00000493795.1:p.His326=
ENST00000646679.1:c.976_978delinsCAT ENSP00000494887.1:p.His326=
ENST00000646822.1:n.2596_2598delinsCAT
ENST00000646940.1:n.1708_1710delinsCAT
ENST00000647286.1:n.1632_1634delinsCAT
ENST00000647477.1:n.273_275delinsCAT
ENST00000399959.6:c.1534_1536delinsCAT ENSP00000382840.2:p.His512=
ENST00000441189.3:c.341-1099_341-1097delinsCAT ENSP00000414281.2:n.341-1099_341-1097delinsCAT
ENST00000457138.6:c.1486_1488delinsCAT ENSP00000392494.2:p.His496=
ENST00000478993.5:c.1534_1536delinsCAT ENSP00000478443.1:p.His512=
ENST00000542215.5:n.1582_1584delinsCAT
ENST00000616050.2:c.87_89delinsCAT
ENST00000625837.2:c.1534_1536delinsCAT ENSP00000486306.1:p.His512=
ENST00000626301.2:c.1534_1536delinsCAT ENSP00000486443.1:p.His512=
ENST00000629496.2:c.1534_1536delinsCAT ENSP00000487224.1:p.His512=
ENST00000629785.2:c.1534_1536delinsCAT ENSP00000486516.1:p.His512=
ENST00000630255.2:c.1534_1536delinsCAT ENSP00000486720.1:p.His512=
ENST00000630370.2:c.1534_1536delinsCAT ENSP00000487062.1:p.His512=
ENST00000630858.2:c.1534_1536delinsCAT ENSP00000486514.1:p.His512=
NM_001193416.2:c.1534_1536delinsCAT NP_001180345.1:p.His512=
NM_001193417.2:c.1486_1488delinsCAT NP_001180346.1:p.His496=
NM_001356.4:c.1534_1536delinsCAT NP_001347.3:p.His512=
NR_126093.1:n.2479_2481delinsCAT
XM_011543892.1:c.1534_1536delinsCAT XP_011542194.1:p.His512=
NM_001363819.1:c.976_978delinsCAT NP_001350748.1:p.His326=
XM_011543892.2:c.1534_1536delinsCAT XP_011542194.1:p.His512=
XM_017029313.1:c.976_978delinsCAT XP_016884802.1:p.His326=
NM_001193416.3:c.1534_1536delinsCAT NP_001180345.1:p.His512=
NM_001193417.3:c.1486_1488delinsCAT NP_001180346.1:p.His496=
NM_001356.5:c.1534_1536delinsCAT MANE Select NP_001347.3:p.His512=