Canonical Allele Identifier: CA2530115544

Gene: USP9X

Linked Data

• gnomAD v4: X-41230438-AAAAGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230442_41230447del , CM000685.2:g.41230442_41230447del	GRCh38
NC_000023.10:g.41089695_41089700del , CM000685.1:g.41089695_41089700del	GRCh37
NC_000023.9:g.40974639_40974644del	NCBI36
NG_012547.1:g.149808_149813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-59_7447-54del	ENSP00000515603.1:n.7447-59_7447-54del
ENST00000703987.1:c.7495-59_7495-54del	ENSP00000515604.1:n.7495-59_7495-54del
ENST00000704649.1:c.3685-1945_3685-1940del	ENSP00000515974.1:n.3685-1945_3685-1940del
ENST00000704650.1:c.7432-59_7432-54del	ENSP00000515975.1:n.7432-59_7432-54del
ENST00000704651.1:c.7279-59_7279-54del	ENSP00000515976.1:n.7279-59_7279-54del
ENST00000704652.1:c.6531-59_6531-54del
ENST00000704654.1:c.4311-59_4311-54del
ENST00000704655.1:c.3575-59_3575-54del	ENSP00000515980.1:n.3575-59_3575-54del
ENST00000704656.1:c.2883-59_2883-54del	ENSP00000515981.1:n.2883-59_2883-54del
ENST00000324545.9:c.7480-59_7480-54del	ENSP00000316357.6:n.7480-59_7480-54del
ENST00000378308.7:c.7432-59_7432-54del MANE Select	ENSP00000367558.2:n.7432-59_7432-54del
ENST00000324545.8:c.7480-59_7480-54del	ENSP00000316357.6:n.7480-59_7480-54del
ENST00000378308.6:c.7432-59_7432-54del	ENSP00000367558.2:n.7432-59_7432-54del
NM_001039590.2:c.7480-59_7480-54del	NP_001034679.2:n.7480-59_7480-54del
NM_001039591.2:c.7432-59_7432-54del	NP_001034680.2:n.7432-59_7432-54del
XM_005272675.3:c.7495-59_7495-54del	XP_005272732.1:n.7495-59_7495-54del
XM_005272676.3:c.7447-59_7447-54del	XP_005272733.1:n.7447-59_7447-54del
XM_005272675.4:c.7495-59_7495-54del	XP_005272732.1:n.7495-59_7495-54del
XM_005272676.4:c.7447-59_7447-54del	XP_005272733.1:n.7447-59_7447-54del
NM_001039591.3:c.7432-59_7432-54del MANE Select	NP_001034680.2:n.7432-59_7432-54del
NM_001039590.3:c.7480-59_7480-54del	NP_001034679.2:n.7480-59_7480-54del