Canonical Allele Identifier: CA10388344

Gene: USP9X

Linked Data

• dbSNP Id: rs761834056
• ExAC: X:40996314 T / TG
• gnomAD v2: X-40996314-T-TG
• gnomAD v3: X-41137061-T-TG
• gnomAD v4: X-41137061-T-TG
• MyVariant Identifiers: chrX:g.40996314_40996315insG (hg19) ; chrX:g.41137061_41137062insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41137061_41137062insG , CM000685.2:g.41137061_41137062insG	GRCh38
NC_000023.10:g.40996314_40996315insG , CM000685.1:g.40996314_40996315insG	GRCh37
NC_000023.9:g.40881258_40881259insG	NCBI36
NG_012547.1:g.56427_56428insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.654+39_654+40insG	ENSP00000515603.1:n.654+39_654+40insG
ENST00000703987.1:c.654+39_654+40insG	ENSP00000515604.1:n.654+39_654+40insG
ENST00000704649.1:c.654+39_654+40insG	ENSP00000515974.1:n.654+39_654+40insG
ENST00000704650.1:c.654+39_654+40insG	ENSP00000515975.1:n.654+39_654+40insG
ENST00000704651.1:c.654+39_654+40insG	ENSP00000515976.1:n.654+39_654+40insG
ENST00000324545.9:c.654+39_654+40insG	ENSP00000316357.6:n.654+39_654+40insG
ENST00000378308.7:c.654+39_654+40insG MANE Select	ENSP00000367558.2:n.654+39_654+40insG
ENST00000324545.8:c.654+39_654+40insG	ENSP00000316357.6:n.654+39_654+40insG
ENST00000378308.6:c.654+39_654+40insG	ENSP00000367558.2:n.654+39_654+40insG
NM_001039590.2:c.654+39_654+40insG	NP_001034679.2:n.654+39_654+40insG
NM_001039591.2:c.654+39_654+40insG	NP_001034680.2:n.654+39_654+40insG
XM_005272675.3:c.654+39_654+40insG	XP_005272732.1:n.654+39_654+40insG
XM_005272676.3:c.654+39_654+40insG	XP_005272733.1:n.654+39_654+40insG
XM_005272675.4:c.654+39_654+40insG	XP_005272732.1:n.654+39_654+40insG
XM_005272676.4:c.654+39_654+40insG	XP_005272733.1:n.654+39_654+40insG
NM_001039591.3:c.654+39_654+40insG MANE Select	NP_001034680.2:n.654+39_654+40insG
NM_001039590.3:c.654+39_654+40insG	NP_001034679.2:n.654+39_654+40insG