Canonical Allele Identifier: CA2693479343

Gene: USP9X

Linked Data

• gnomAD v4: X-41214541-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41214541T>A , CM000685.2:g.41214541T>A	GRCh38
NC_000023.10:g.41073794T>A , CM000685.1:g.41073794T>A	GRCh37
NC_000023.9:g.40958738T>A	NCBI36
NG_012547.1:g.133907T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.5205-27T>A	ENSP00000515603.1:n.5205-27T>A
ENST00000703987.1:c.5205-27T>A	ENSP00000515604.1:n.5205-27T>A
ENST00000704649.1:c.3685-17846T>A	ENSP00000515974.1:n.3685-17846T>A
ENST00000704650.1:c.5190-27T>A	ENSP00000515975.1:n.5190-27T>A
ENST00000704651.1:c.5037-27T>A	ENSP00000515976.1:n.5037-27T>A
ENST00000704652.1:c.4289-27T>A
ENST00000704654.1:c.2144-27T>A
ENST00000704655.1:c.1333-27T>A	ENSP00000515980.1:n.1333-27T>A
ENST00000704656.1:c.783-1358T>A	ENSP00000515981.1:n.783-1358T>A
ENST00000324545.9:c.5190-27T>A	ENSP00000316357.6:n.5190-27T>A
ENST00000378308.7:c.5190-27T>A MANE Select	ENSP00000367558.2:n.5190-27T>A
ENST00000324545.8:c.5190-27T>A	ENSP00000316357.6:n.5190-27T>A
ENST00000378308.6:c.5190-27T>A	ENSP00000367558.2:n.5190-27T>A
NM_001039590.2:c.5190-27T>A	NP_001034679.2:n.5190-27T>A
NM_001039591.2:c.5190-27T>A	NP_001034680.2:n.5190-27T>A
XM_005272675.3:c.5205-27T>A	XP_005272732.1:n.5205-27T>A
XM_005272676.3:c.5205-27T>A	XP_005272733.1:n.5205-27T>A
XM_005272675.4:c.5205-27T>A	XP_005272732.1:n.5205-27T>A
XM_005272676.4:c.5205-27T>A	XP_005272733.1:n.5205-27T>A
NM_001039591.3:c.5190-27T>A MANE Select	NP_001034680.2:n.5190-27T>A
NM_001039590.3:c.5190-27T>A	NP_001034679.2:n.5190-27T>A