Canonical Allele Identifier: CA516347601

Gene: DDX3X

Linked Data

• MyVariant Identifiers: chrX:g.41204689C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41345436C>A , CM000685.2:g.41345436C>A	GRCh38
NC_000023.10:g.41204689C>A , CM000685.1:g.41204689C>A	GRCh37
NC_000023.9:g.41089633C>A	NCBI36
NG_012830.1:g.17039C>A
NG_012830.2:g.17039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1335C>A	ENSP00000496052.2:p.Ile445=
ENST00000399959.7:c.1200C>A	ENSP00000382840.3:p.Ile400=
ENST00000441189.4:c.1104C>A	ENSP00000414281.3:p.Ile368=
ENST00000457138.7:c.1155C>A	ENSP00000392494.2:p.Ile385=
ENST00000629496.3:c.1203C>A	ENSP00000487224.1:p.Ile401=
ENST00000642161.1:n.3402C>A
ENST00000642322.1:c.645C>A	ENSP00000496052.1:p.Ile215=
ENST00000642424.1:c.645C>A	ENSP00000496356.1:p.Ile215=
ENST00000642589.1:n.4525C>A
ENST00000642597.1:n.1377C>A
ENST00000642687.1:n.1236C>A
ENST00000642722.1:n.2036C>A
ENST00000642763.1:n.2094C>A
ENST00000642793.1:c.*652C>A	ENSP00000493976.1:n.*652C>A
ENST00000642801.1:n.852C>A
ENST00000643820.1:n.479C>A
ENST00000643963.1:c.*485C>A	ENSP00000495264.1:n.*485C>A
ENST00000644073.1:c.1161C>A	ENSP00000493475.1:p.Ile387=
ENST00000644074.1:c.1200C>A	ENSP00000496663.1:p.Ile400=
ENST00000644109.1:c.1365C>A	ENSP00000494952.1:p.Ile455=
ENST00000644307.1:n.1373C>A
ENST00000644513.1:c.1203C>A	ENSP00000493819.1:p.Ile401=
ENST00000644677.1:c.1086C>A	ENSP00000496524.1:p.Ile362=
ENST00000644876.2:c.1203C>A MANE Select	ENSP00000494040.1:p.Ile401=
ENST00000644958.1:n.2864C>A
ENST00000645080.1:c.*2425C>A	ENSP00000494767.1:n.*2425C>A
ENST00000645120.1:n.2698C>A
ENST00000645338.1:n.1373C>A
ENST00000645380.1:n.2667C>A
ENST00000645561.1:n.2379C>A
ENST00000645574.1:n.4067C>A
ENST00000645589.1:c.1203C>A	ENSP00000494588.1:p.Ile401=
ENST00000646093.1:n.387C>A
ENST00000646107.1:c.1086C>A	ENSP00000494518.1:p.Ile362=
ENST00000646122.1:c.1203C>A	ENSP00000496222.1:p.Ile401=
ENST00000646196.1:n.2172C>A
ENST00000646223.1:c.*1196C>A	ENSP00000496043.1:n.*1196C>A
ENST00000646319.1:c.1203C>A	ENSP00000495377.1:p.Ile401=
ENST00000646390.1:n.3491C>A
ENST00000646627.1:c.645C>A	ENSP00000493795.1:p.Ile215=
ENST00000646679.1:c.645C>A	ENSP00000494887.1:p.Ile215=
ENST00000646822.1:n.2265C>A
ENST00000646940.1:n.1377C>A
ENST00000647286.1:n.1301C>A
ENST00000399959.6:c.1203C>A	ENSP00000382840.2:p.Ile401=
ENST00000441189.3:c.341-2204C>A	ENSP00000414281.2:n.341-2204C>A
ENST00000457138.6:c.1155C>A	ENSP00000392494.2:p.Ile385=
ENST00000478993.5:c.1203C>A	ENSP00000478443.1:p.Ile401=
ENST00000542215.5:n.1251C>A
ENST00000625837.2:c.1203C>A	ENSP00000486306.1:p.Ile401=
ENST00000626301.2:c.1203C>A	ENSP00000486443.1:p.Ile401=
ENST00000629496.2:c.1203C>A	ENSP00000487224.1:p.Ile401=
ENST00000629785.2:c.1203C>A	ENSP00000486516.1:p.Ile401=
ENST00000630255.2:c.1203C>A	ENSP00000486720.1:p.Ile401=
ENST00000630370.2:c.1203C>A	ENSP00000487062.1:p.Ile401=
ENST00000630858.2:c.1203C>A	ENSP00000486514.1:p.Ile401=
NM_001193416.2:c.1203C>A	NP_001180345.1:p.Ile401=
NM_001193417.2:c.1155C>A	NP_001180346.1:p.Ile385=
NM_001356.4:c.1203C>A	NP_001347.3:p.Ile401=
NR_126093.1:n.2148C>A
XM_011543892.1:c.1203C>A	XP_011542194.1:p.Ile401=
NM_001363819.1:c.645C>A	NP_001350748.1:p.Ile215=
XM_011543892.2:c.1203C>A	XP_011542194.1:p.Ile401=
XM_017029313.1:c.645C>A	XP_016884802.1:p.Ile215=
NM_001193416.3:c.1203C>A	NP_001180345.1:p.Ile401=
NM_001193417.3:c.1155C>A	NP_001180346.1:p.Ile385=
NM_001356.5:c.1203C>A MANE Select	NP_001347.3:p.Ile401=