Canonical Allele Identifier: CA10389220

Gene: USP9X

Linked Data

• dbSNP Id: rs748590227
• ExAC: X:41089709 TGA / T
• gnomAD v2: X-41089709-TGA-T
• gnomAD v3: X-41230456-TGA-T
• gnomAD v4: X-41230456-TGA-T
• MyVariant Identifiers: chrX:g.41089710_41089711del (hg19) ; chrX:g.41230457_41230458del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230458_41230459del , CM000685.2:g.41230458_41230459del	GRCh38
NC_000023.10:g.41089711_41089712del , CM000685.1:g.41089711_41089712del	GRCh37
NC_000023.9:g.40974655_40974656del	NCBI36
NG_012547.1:g.149824_149825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-43_7447-42del	ENSP00000515603.1:n.7447-43_7447-42del
ENST00000703987.1:c.7495-43_7495-42del	ENSP00000515604.1:n.7495-43_7495-42del
ENST00000704649.1:c.3685-1929_3685-1928del	ENSP00000515974.1:n.3685-1929_3685-1928del
ENST00000704650.1:c.7432-43_7432-42del	ENSP00000515975.1:n.7432-43_7432-42del
ENST00000704651.1:c.7279-43_7279-42del	ENSP00000515976.1:n.7279-43_7279-42del
ENST00000704652.1:c.6531-43_6531-42del
ENST00000704654.1:c.4311-43_4311-42del
ENST00000704655.1:c.3575-43_3575-42del	ENSP00000515980.1:n.3575-43_3575-42del
ENST00000704656.1:c.2883-43_2883-42del	ENSP00000515981.1:n.2883-43_2883-42del
ENST00000324545.9:c.7480-43_7480-42del	ENSP00000316357.6:n.7480-43_7480-42del
ENST00000378308.7:c.7432-43_7432-42del MANE Select	ENSP00000367558.2:n.7432-43_7432-42del
ENST00000324545.8:c.7480-43_7480-42del	ENSP00000316357.6:n.7480-43_7480-42del
ENST00000378308.6:c.7432-43_7432-42del	ENSP00000367558.2:n.7432-43_7432-42del
NM_001039590.2:c.7480-43_7480-42del	NP_001034679.2:n.7480-43_7480-42del
NM_001039591.2:c.7432-43_7432-42del	NP_001034680.2:n.7432-43_7432-42del
XM_005272675.3:c.7495-43_7495-42del	XP_005272732.1:n.7495-43_7495-42del
XM_005272676.3:c.7447-43_7447-42del	XP_005272733.1:n.7447-43_7447-42del
XM_005272675.4:c.7495-43_7495-42del	XP_005272732.1:n.7495-43_7495-42del
XM_005272676.4:c.7447-43_7447-42del	XP_005272733.1:n.7447-43_7447-42del
NM_001039591.3:c.7432-43_7432-42del MANE Select	NP_001034680.2:n.7432-43_7432-42del
NM_001039590.3:c.7480-43_7480-42del	NP_001034679.2:n.7480-43_7480-42del