Canonical Allele Identifier: CA412776540

Gene: DDX3X

Linked Data

• dbSNP Id: rs1311231381
• gnomAD v3: X-41346551-A-G
• gnomAD v4: X-41346551-A-G
• MyVariant Identifiers: chrX:g.41205804A>G (hg19) ; chrX:g.41346551A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41346551A>G , CM000685.2:g.41346551A>G	GRCh38
NC_000023.10:g.41205804A>G , CM000685.1:g.41205804A>G	GRCh37
NC_000023.9:g.41090748A>G	NCBI36
NG_012830.1:g.18154A>G
NG_012830.2:g.18154A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642322.2:c.1676A>G	ENSP00000496052.2:p.Asn559Ser
ENST00000399959.7:c.1541A>G	ENSP00000382840.3:p.Asn514Ser
ENST00000441189.4:c.1445A>G	ENSP00000414281.3:p.Asn482Ser
ENST00000457138.7:c.1496A>G	ENSP00000392494.2:p.Asn499Ser
ENST00000611968.2:c.138A>G
ENST00000616050.3:c.292A>G
ENST00000629496.3:c.1544A>G	ENSP00000487224.1:p.Asn515Ser
ENST00000642161.1:n.3743A>G
ENST00000642322.1:c.986A>G	ENSP00000496052.1:p.Asn329Ser
ENST00000642424.1:c.986A>G	ENSP00000496356.1:p.Asn329Ser
ENST00000642589.1:n.4866A>G
ENST00000642597.1:n.1718A>G
ENST00000642687.1:n.1577A>G
ENST00000642722.1:n.2377A>G
ENST00000642763.1:n.2435A>G
ENST00000642793.1:c.*993A>G	ENSP00000493976.1:n.*993A>G
ENST00000642801.1:n.1193A>G
ENST00000643820.1:n.914A>G
ENST00000643963.1:c.*826A>G	ENSP00000495264.1:n.*826A>G
ENST00000644073.1:c.1502A>G	ENSP00000493475.1:p.Asn501Ser
ENST00000644074.1:c.1541A>G	ENSP00000496663.1:p.Asn514Ser
ENST00000644109.1:c.1706A>G	ENSP00000494952.1:p.Asn569Ser
ENST00000644307.1:n.1714A>G
ENST00000644513.1:c.1544A>G	ENSP00000493819.1:p.Asn515Ser
ENST00000644677.1:c.1427A>G	ENSP00000496524.1:p.Asn476Ser
ENST00000644876.2:c.1544A>G MANE Select	ENSP00000494040.1:p.Asn515Ser
ENST00000644958.1:n.3205A>G
ENST00000645080.1:c.*2766A>G	ENSP00000494767.1:n.*2766A>G
ENST00000645120.1:n.3039A>G
ENST00000645338.1:n.1714A>G
ENST00000645380.1:n.3008A>G
ENST00000645561.1:n.2720A>G
ENST00000645574.1:n.4408A>G
ENST00000645589.1:c.*43A>G	ENSP00000494588.1:n.*43A>G
ENST00000646107.1:c.1427A>G	ENSP00000494518.1:p.Asn476Ser
ENST00000646122.1:c.1544A>G	ENSP00000496222.1:p.Asn515Ser
ENST00000646196.1:n.2513A>G
ENST00000646223.1:c.*1537A>G	ENSP00000496043.1:n.*1537A>G
ENST00000646319.1:c.1544A>G	ENSP00000495377.1:p.Asn515Ser
ENST00000646390.1:n.3832A>G
ENST00000646627.1:c.986A>G	ENSP00000493795.1:p.Asn329Ser
ENST00000646679.1:c.986A>G	ENSP00000494887.1:p.Asn329Ser
ENST00000646822.1:n.2606A>G
ENST00000646940.1:n.1718A>G
ENST00000647286.1:n.1642A>G
ENST00000647477.1:n.283A>G
ENST00000399959.6:c.1544A>G	ENSP00000382840.2:p.Asn515Ser
ENST00000441189.3:c.341-1089A>G	ENSP00000414281.2:n.341-1089A>G
ENST00000457138.6:c.1496A>G	ENSP00000392494.2:p.Asn499Ser
ENST00000478993.5:c.1544A>G	ENSP00000478443.1:p.Asn515Ser
ENST00000542215.5:n.1592A>G
ENST00000616050.2:c.97A>G
ENST00000625837.2:c.1544A>G	ENSP00000486306.1:p.Asn515Ser
ENST00000626301.2:c.1544A>G	ENSP00000486443.1:p.Asn515Ser
ENST00000629496.2:c.1544A>G	ENSP00000487224.1:p.Asn515Ser
ENST00000629785.2:c.1544A>G	ENSP00000486516.1:p.Asn515Ser
ENST00000630255.2:c.1544A>G	ENSP00000486720.1:p.Asn515Ser
ENST00000630370.2:c.1544A>G	ENSP00000487062.1:p.Asn515Ser
ENST00000630858.2:c.1544A>G	ENSP00000486514.1:p.Asn515Ser
NM_001193416.2:c.1544A>G	NP_001180345.1:p.Asn515Ser
NM_001193417.2:c.1496A>G	NP_001180346.1:p.Asn499Ser
NM_001356.4:c.1544A>G	NP_001347.3:p.Asn515Ser
NR_126093.1:n.2489A>G
XM_011543892.1:c.1544A>G	XP_011542194.1:p.Asn515Ser
NM_001363819.1:c.986A>G	NP_001350748.1:p.Asn329Ser
XM_011543892.2:c.1544A>G	XP_011542194.1:p.Asn515Ser
XM_017029313.1:c.986A>G	XP_016884802.1:p.Asn329Ser
NM_001193416.3:c.1544A>G	NP_001180345.1:p.Asn515Ser
NM_001193417.3:c.1496A>G	NP_001180346.1:p.Asn499Ser
NM_001356.5:c.1544A>G MANE Select	NP_001347.3:p.Asn515Ser