Canonical Allele Identifier: CA2579588226

Gene: USP9X

Linked Data

• gnomAD v4: X-41230402-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230402C>T , CM000685.2:g.41230402C>T	GRCh38
NC_000023.10:g.41089655C>T , CM000685.1:g.41089655C>T	GRCh37
NC_000023.9:g.40974599C>T	NCBI36
NG_012547.1:g.149768C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-99C>T	ENSP00000515603.1:n.7447-99C>T
ENST00000703987.1:c.7495-99C>T	ENSP00000515604.1:n.7495-99C>T
ENST00000704649.1:c.3685-1985C>T	ENSP00000515974.1:n.3685-1985C>T
ENST00000704650.1:c.7432-99C>T	ENSP00000515975.1:n.7432-99C>T
ENST00000704651.1:c.7279-99C>T	ENSP00000515976.1:n.7279-99C>T
ENST00000704652.1:c.6531-99C>T
ENST00000704654.1:c.4311-99C>T
ENST00000704655.1:c.3575-99C>T	ENSP00000515980.1:n.3575-99C>T
ENST00000704656.1:c.2883-99C>T	ENSP00000515981.1:n.2883-99C>T
ENST00000324545.9:c.7480-99C>T	ENSP00000316357.6:n.7480-99C>T
ENST00000378308.7:c.7432-99C>T MANE Select	ENSP00000367558.2:n.7432-99C>T
ENST00000324545.8:c.7480-99C>T	ENSP00000316357.6:n.7480-99C>T
ENST00000378308.6:c.7432-99C>T	ENSP00000367558.2:n.7432-99C>T
NM_001039590.2:c.7480-99C>T	NP_001034679.2:n.7480-99C>T
NM_001039591.2:c.7432-99C>T	NP_001034680.2:n.7432-99C>T
XM_005272675.3:c.7495-99C>T	XP_005272732.1:n.7495-99C>T
XM_005272676.3:c.7447-99C>T	XP_005272733.1:n.7447-99C>T
XM_005272675.4:c.7495-99C>T	XP_005272732.1:n.7495-99C>T
XM_005272676.4:c.7447-99C>T	XP_005272733.1:n.7447-99C>T
NM_001039591.3:c.7432-99C>T MANE Select	NP_001034680.2:n.7432-99C>T
NM_001039590.3:c.7480-99C>T	NP_001034679.2:n.7480-99C>T