Canonical Allele Identifier: CA329005972
Gene: USP9X HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.41123184G>A
GRCh37 chrX:g.40982437G>A
gnomAD v2:
X:40982437 G / A
gnomAD v3:
X:41123184 G / A
gnomAD v4:
chrX-41123184-G-A
Joint Max Group AF 0.11931412 (NFE)
Genomes Max Group AF 0.11931412 (NFE)
ClinVar RCV:
RCV001654291
ClinVar Variation:
1246199
dbSNP:
1263921
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41123184G>A , CM000685.2:g.41123184G>A GRCh38
NC_000023.10:g.40982437G>A , CM000685.1:g.40982437G>A GRCh37
NC_000023.9:g.40867381G>A NCBI36
NG_012547.1:g.42550G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703986.1:c.-158-287G>A ENSP00000515603.1:n.-158-287G>A
ENST00000703987.1:c.-158-287G>A ENSP00000515604.1:n.-158-287G>A
ENST00000704649.1:c.-158-287G>A ENSP00000515974.1:n.-158-287G>A
ENST00000704650.1:c.-158-287G>A ENSP00000515975.1:n.-158-287G>A
ENST00000704651.1:c.-158-287G>A ENSP00000515976.1:n.-158-287G>A
ENST00000324545.9:c.-158-287G>A ENSP00000316357.6:n.-158-287G>A
ENST00000378308.7:c.-158-287G>A MANE Select ENSP00000367558.2:n.-158-287G>A
ENST00000324545.8:c.-158-287G>A ENSP00000316357.6:n.-158-287G>A
ENST00000378308.6:c.-158-287G>A ENSP00000367558.2:n.-158-287G>A
NM_001039590.2:c.-158-287G>A NP_001034679.2:n.-158-287G>A
NM_001039591.2:c.-158-287G>A NP_001034680.2:n.-158-287G>A
XM_005272675.3:c.-158-287G>A XP_005272732.1:n.-158-287G>A
XM_005272676.3:c.-158-287G>A XP_005272733.1:n.-158-287G>A
XM_005272675.4:c.-158-287G>A XP_005272732.1:n.-158-287G>A
XM_005272676.4:c.-158-287G>A XP_005272733.1:n.-158-287G>A
NM_001039591.3:c.-158-287G>A MANE Select NP_001034680.2:n.-158-287G>A
NM_001039590.3:c.-158-287G>A NP_001034679.2:n.-158-287G>A
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