Canonical Allele Identifier: CA2425838721
Gene: USP9X HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41230357_41230364delinsTCCCCAAG , CM000685.2:g.41230357_41230364delinsTCCCCAAG GRCh38
NC_000023.10:g.41089610_41089617delinsTCCCCAAG , CM000685.1:g.41089610_41089617delinsTCCCCAAG GRCh37
NC_000023.9:g.40974554_40974561delinsTCCCCAAG NCBI36
NG_012547.1:g.149723_149730delinsTCCCCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000703986.1:c.7447-144_7447-137delinsTCCCCAAG ENSP00000515603.1:n.7447-144_7447-137delinsTCCCCAAG
ENST00000703987.1:c.7495-144_7495-137delinsTCCCCAAG ENSP00000515604.1:n.7495-144_7495-137delinsTCCCCAAG
ENST00000704649.1:c.3685-2030_3685-2023delinsTCCCCAAG ENSP00000515974.1:n.3685-2030_3685-2023delinsTCCCCAAG
ENST00000704650.1:c.7432-144_7432-137delinsTCCCCAAG ENSP00000515975.1:n.7432-144_7432-137delinsTCCCCAAG
ENST00000704651.1:c.7279-144_7279-137delinsTCCCCAAG ENSP00000515976.1:n.7279-144_7279-137delinsTCCCCAAG
ENST00000704652.1:c.6531-144_6531-137delinsTCCCCAAG
ENST00000704654.1:c.4311-144_4311-137delinsTCCCCAAG
ENST00000704655.1:c.3575-144_3575-137delinsTCCCCAAG ENSP00000515980.1:n.3575-144_3575-137delinsTCCCCAAG
ENST00000704656.1:c.2883-144_2883-137delinsTCCCCAAG ENSP00000515981.1:n.2883-144_2883-137delinsTCCCCAAG
ENST00000324545.9:c.7480-144_7480-137delinsTCCCCAAG ENSP00000316357.6:n.7480-144_7480-137delinsTCCCCAAG
ENST00000378308.7:c.7432-144_7432-137delinsTCCCCAAG MANE Select ENSP00000367558.2:n.7432-144_7432-137delinsTCCCCAAG
ENST00000324545.8:c.7480-144_7480-137delinsTCCCCAAG ENSP00000316357.6:n.7480-144_7480-137delinsTCCCCAAG
ENST00000378308.6:c.7432-144_7432-137delinsTCCCCAAG ENSP00000367558.2:n.7432-144_7432-137delinsTCCCCAAG
NM_001039590.2:c.7480-144_7480-137delinsTCCCCAAG NP_001034679.2:n.7480-144_7480-137delinsTCCCCAAG
NM_001039591.2:c.7432-144_7432-137delinsTCCCCAAG NP_001034680.2:n.7432-144_7432-137delinsTCCCCAAG
XM_005272675.3:c.7495-144_7495-137delinsTCCCCAAG XP_005272732.1:n.7495-144_7495-137delinsTCCCCAAG
XM_005272676.3:c.7447-144_7447-137delinsTCCCCAAG XP_005272733.1:n.7447-144_7447-137delinsTCCCCAAG
XM_005272675.4:c.7495-144_7495-137delinsTCCCCAAG XP_005272732.1:n.7495-144_7495-137delinsTCCCCAAG
XM_005272676.4:c.7447-144_7447-137delinsTCCCCAAG XP_005272733.1:n.7447-144_7447-137delinsTCCCCAAG
NM_001039591.3:c.7432-144_7432-137delinsTCCCCAAG MANE Select NP_001034680.2:n.7432-144_7432-137delinsTCCCCAAG
NM_001039590.3:c.7480-144_7480-137delinsTCCCCAAG NP_001034679.2:n.7480-144_7480-137delinsTCCCCAAG