Canonical Allele Identifier: CA412762663

Gene: USP9X

Linked Data

• ClinVar Variation Id: 2894959
• ClinVar RCV Id: RCV003728135
• dbSNP Id: rs1411236915
• gnomAD v2: X-40996069-A-T
• gnomAD v4: X-41136816-A-T
• MyVariant Identifiers: chrX:g.40996069A>T (hg19) ; chrX:g.41136816A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41136816A>T , CM000685.2:g.41136816A>T	GRCh38
NC_000023.10:g.40996069A>T , CM000685.1:g.40996069A>T	GRCh37
NC_000023.9:g.40881013A>T	NCBI36
NG_012547.1:g.56182A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.448A>T	ENSP00000515603.1:p.Asn150Tyr
ENST00000703987.1:c.448A>T	ENSP00000515604.1:p.Asn150Tyr
ENST00000704649.1:c.448A>T	ENSP00000515974.1:p.Asn150Tyr
ENST00000704650.1:c.448A>T	ENSP00000515975.1:p.Asn150Tyr
ENST00000704651.1:c.448A>T	ENSP00000515976.1:p.Asn150Tyr
ENST00000324545.9:c.448A>T	ENSP00000316357.6:p.Asn150Tyr
ENST00000378308.7:c.448A>T MANE Select	ENSP00000367558.2:p.Asn150Tyr
ENST00000324545.8:c.448A>T	ENSP00000316357.6:p.Asn150Tyr
ENST00000378308.6:c.448A>T	ENSP00000367558.2:p.Asn150Tyr
NM_001039590.2:c.448A>T	NP_001034679.2:p.Asn150Tyr
NM_001039591.2:c.448A>T	NP_001034680.2:p.Asn150Tyr
XM_005272675.3:c.448A>T	XP_005272732.1:p.Asn150Tyr
XM_005272676.3:c.448A>T	XP_005272733.1:p.Asn150Tyr
XM_005272675.4:c.448A>T	XP_005272732.1:p.Asn150Tyr
XM_005272676.4:c.448A>T	XP_005272733.1:p.Asn150Tyr
NM_001039591.3:c.448A>T MANE Select	NP_001034680.2:p.Asn150Tyr
NM_001039590.3:c.448A>T	NP_001034679.2:p.Asn150Tyr