Canonical Allele Identifier: CA2579984161

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41219213del , CM000685.2:g.41219213del	GRCh38
NC_000023.10:g.41078466del , CM000685.1:g.41078466del	GRCh37
NC_000023.9:g.40963410del	NCBI36
NG_012547.1:g.138579del

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.6547del MANE Select	NP_001034680.2:p.Val2183Ter
ENST00000378308.7:c.6547del MANE Select	ENSP00000367558.2:p.Val2183Ter
NM_001039590.2:c.6547del	NP_001034679.2:p.Val2183Ter
NM_001039590.3:c.6547del	NP_001034679.2:p.Val2183Ter
NM_001039591.2:c.6547del	NP_001034680.2:p.Val2183Ter
ENST00000324545.8:c.6547del	ENSP00000316357.6:p.Val2183Ter
ENST00000324545.9:c.6547del	ENSP00000316357.6:p.Val2183Ter
ENST00000378308.6:c.6547del	ENSP00000367558.2:p.Val2183Ter
ENST00000703986.1:c.6562del	ENSP00000515603.1:p.Val2188Ter
ENST00000703987.1:c.6562del	ENSP00000515604.1:p.Val2188Ter
ENST00000704649.1:c.3685-13174del	ENSP00000515974.1:n.3685-13174del
ENST00000704650.1:c.6547del	ENSP00000515975.1:p.Val2183Ter
ENST00000704651.1:c.6394del	ENSP00000515976.1:p.Val2132Ter
ENST00000704652.1:c.5646del
ENST00000704654.1:c.3501del
ENST00000704655.1:c.2690del	ENSP00000515980.1:n.2690del
ENST00000704656.1:c.1998del	ENSP00000515981.1:n.1998del
XM_005272675.3:c.6562del	XP_005272732.1:p.Val2188Ter
XM_005272675.4:c.6562del	XP_005272732.1:p.Val2188Ter
XM_005272676.3:c.6562del	XP_005272733.1:p.Val2188Ter
XM_005272676.4:c.6562del	XP_005272733.1:p.Val2188Ter