Canonical Allele Identifier: CA329012427

Gene: USP9X

Linked Data

• dbSNP Id: rs749990813
• gnomAD v2: X-40996413-G-A
• gnomAD v3: X-41137160-G-A
• gnomAD v4: X-41137160-G-A
• MyVariant Identifiers: chrX:g.40996413G>A (hg19) ; chrX:g.41137160G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41137160G>A , CM000685.2:g.41137160G>A	GRCh38
NC_000023.10:g.40996413G>A , CM000685.1:g.40996413G>A	GRCh37
NC_000023.9:g.40881357G>A	NCBI36
NG_012547.1:g.56526G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.654+138G>A	ENSP00000515603.1:n.654+138G>A
ENST00000703987.1:c.654+138G>A	ENSP00000515604.1:n.654+138G>A
ENST00000704649.1:c.654+138G>A	ENSP00000515974.1:n.654+138G>A
ENST00000704650.1:c.654+138G>A	ENSP00000515975.1:n.654+138G>A
ENST00000704651.1:c.654+138G>A	ENSP00000515976.1:n.654+138G>A
ENST00000324545.9:c.654+138G>A	ENSP00000316357.6:n.654+138G>A
ENST00000378308.7:c.654+138G>A MANE Select	ENSP00000367558.2:n.654+138G>A
ENST00000324545.8:c.654+138G>A	ENSP00000316357.6:n.654+138G>A
ENST00000378308.6:c.654+138G>A	ENSP00000367558.2:n.654+138G>A
NM_001039590.2:c.654+138G>A	NP_001034679.2:n.654+138G>A
NM_001039591.2:c.654+138G>A	NP_001034680.2:n.654+138G>A
XM_005272675.3:c.654+138G>A	XP_005272732.1:n.654+138G>A
XM_005272676.3:c.654+138G>A	XP_005272733.1:n.654+138G>A
XM_005272675.4:c.654+138G>A	XP_005272732.1:n.654+138G>A
XM_005272676.4:c.654+138G>A	XP_005272733.1:n.654+138G>A
NM_001039591.3:c.654+138G>A MANE Select	NP_001034680.2:n.654+138G>A
NM_001039590.3:c.654+138G>A	NP_001034679.2:n.654+138G>A