Canonical Allele Identifier: CA16608923
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 384654
ClinVar RCV Id: RCV000430135 RCV001329531
dbSNP Id: rs1057522024
gnomAD v4: X-41144518-A-G
MyVariant Identifiers: chrX:g.41003771A>G (hg19) chrX:g.41144518A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41144518A>G , CM000685.2:g.41144518A>G GRCh38
NC_000023.10:g.41003771A>G , CM000685.1:g.41003771A>G GRCh37
NC_000023.9:g.40888715A>G NCBI36
NG_012547.1:g.63884A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.1315-4A>G ENSP00000515603.1:n.1315-4A>G
ENST00000703987.1:c.1315-4A>G ENSP00000515604.1:n.1315-4A>G
ENST00000704649.1:c.1315-4A>G ENSP00000515974.1:n.1315-4A>G
ENST00000704650.1:c.1315-4A>G ENSP00000515975.1:n.1315-4A>G
ENST00000704651.1:c.1162-4A>G ENSP00000515976.1:n.1162-4A>G
ENST00000704652.1:c.545-4A>G
ENST00000324545.9:c.1315-4A>G ENSP00000316357.6:n.1315-4A>G
ENST00000378308.7:c.1315-4A>G MANE Select ENSP00000367558.2:n.1315-4A>G
ENST00000324545.8:c.1315-4A>G ENSP00000316357.6:n.1315-4A>G
ENST00000378308.6:c.1315-4A>G ENSP00000367558.2:n.1315-4A>G
NM_001039590.2:c.1315-4A>G NP_001034679.2:n.1315-4A>G
NM_001039591.2:c.1315-4A>G NP_001034680.2:n.1315-4A>G
XM_005272675.3:c.1315-4A>G XP_005272732.1:n.1315-4A>G
XM_005272676.3:c.1315-4A>G XP_005272733.1:n.1315-4A>G
XM_005272675.4:c.1315-4A>G XP_005272732.1:n.1315-4A>G
XM_005272676.4:c.1315-4A>G XP_005272733.1:n.1315-4A>G
NM_001039591.3:c.1315-4A>G MANE Select NP_001034680.2:n.1315-4A>G
NM_001039590.3:c.1315-4A>G NP_001034679.2:n.1315-4A>G
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