Canonical Allele Identifier: CA875373484
Gene: USP9X HGNC NCBI

Linked Data

dbSNP Id: rs1402157352

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41230343_41230357del , CM000685.2:g.41230343_41230357del GRCh38
NC_000023.10:g.41089596_41089610del , CM000685.1:g.41089596_41089610del GRCh37
NC_000023.9:g.40974540_40974554del NCBI36
NG_012547.1:g.149709_149723del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703986.1:c.7447-158_7447-144del ENSP00000515603.1:n.7447-158_7447-144del
ENST00000703987.1:c.7495-158_7495-144del ENSP00000515604.1:n.7495-158_7495-144del
ENST00000704649.1:c.3685-2044_3685-2030del ENSP00000515974.1:n.3685-2044_3685-2030del
ENST00000704650.1:c.7432-158_7432-144del ENSP00000515975.1:n.7432-158_7432-144del
ENST00000704651.1:c.7279-158_7279-144del ENSP00000515976.1:n.7279-158_7279-144del
ENST00000704652.1:c.6531-158_6531-144del
ENST00000704654.1:c.4311-158_4311-144del
ENST00000704655.1:c.3575-158_3575-144del ENSP00000515980.1:n.3575-158_3575-144del
ENST00000704656.1:c.2883-158_2883-144del ENSP00000515981.1:n.2883-158_2883-144del
ENST00000324545.9:c.7480-158_7480-144del ENSP00000316357.6:n.7480-158_7480-144del
ENST00000378308.7:c.7432-158_7432-144del MANE Select ENSP00000367558.2:n.7432-158_7432-144del
ENST00000324545.8:c.7480-158_7480-144del ENSP00000316357.6:n.7480-158_7480-144del
ENST00000378308.6:c.7432-158_7432-144del ENSP00000367558.2:n.7432-158_7432-144del
NM_001039590.2:c.7480-158_7480-144del NP_001034679.2:n.7480-158_7480-144del
NM_001039591.2:c.7432-158_7432-144del NP_001034680.2:n.7432-158_7432-144del
XM_005272675.3:c.7495-158_7495-144del XP_005272732.1:n.7495-158_7495-144del
XM_005272676.3:c.7447-158_7447-144del XP_005272733.1:n.7447-158_7447-144del
XM_005272675.4:c.7495-158_7495-144del XP_005272732.1:n.7495-158_7495-144del
XM_005272676.4:c.7447-158_7447-144del XP_005272733.1:n.7447-158_7447-144del
NM_001039591.3:c.7432-158_7432-144del MANE Select NP_001034680.2:n.7432-158_7432-144del
NM_001039590.3:c.7480-158_7480-144del NP_001034679.2:n.7480-158_7480-144del