Canonical Allele Identifier: CA328995928

Gene: USP9X

Linked Data

• dbSNP Id: rs982087910
• gnomAD v4: X-41229313-G-A
• MyVariant Identifiers: chrX:g.41088566G>A (hg19) ; chrX:g.41229313G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229313G>A , CM000685.2:g.41229313G>A	GRCh38
NC_000023.10:g.41088566G>A , CM000685.1:g.41088566G>A	GRCh37
NC_000023.9:g.40973510G>A	NCBI36
NG_012547.1:g.148679G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7137G>A	ENSP00000515603.1:p.Gln2379=
ENST00000703987.1:c.7137G>A	ENSP00000515604.1:p.Gln2379=
ENST00000704649.1:c.3685-3074G>A	ENSP00000515974.1:n.3685-3074G>A
ENST00000704650.1:c.7122G>A	ENSP00000515975.1:p.Gln2374=
ENST00000704651.1:c.6969G>A	ENSP00000515976.1:p.Gln2323=
ENST00000704652.1:c.6221G>A
ENST00000704654.1:c.4001G>A
ENST00000704655.1:c.3265G>A	ENSP00000515980.1:n.3265G>A
ENST00000704656.1:c.2573G>A	ENSP00000515981.1:n.2573G>A
ENST00000324545.9:c.7122G>A	ENSP00000316357.6:p.Gln2374=
ENST00000378308.7:c.7122G>A MANE Select	ENSP00000367558.2:p.Gln2374=
ENST00000324545.8:c.7122G>A	ENSP00000316357.6:p.Gln2374=
ENST00000378308.6:c.7122G>A	ENSP00000367558.2:p.Gln2374=
ENST00000485180.1:n.331G>A
NM_001039590.2:c.7122G>A	NP_001034679.2:p.Gln2374=
NM_001039591.2:c.7122G>A	NP_001034680.2:p.Gln2374=
XM_005272675.3:c.7137G>A	XP_005272732.1:p.Gln2379=
XM_005272676.3:c.7137G>A	XP_005272733.1:p.Gln2379=
XM_005272675.4:c.7137G>A	XP_005272732.1:p.Gln2379=
XM_005272676.4:c.7137G>A	XP_005272733.1:p.Gln2379=
NM_001039591.3:c.7122G>A MANE Select	NP_001034680.2:p.Gln2374=
NM_001039590.3:c.7122G>A	NP_001034679.2:p.Gln2374=