Canonical Allele Identifier: CA1132546849

Gene: USP9X

Linked Data

• gnomAD v3: X-41230364-G-GTTTTTTTTTTTT
• gnomAD v4: X-41230364-G-GTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230366_41230367insTTTTTTTTTTTT , CM000685.2:g.41230366_41230367insTTTTTTTTTTTT	GRCh38
NC_000023.10:g.41089619_41089620insTTTTTTTTTTTT , CM000685.1:g.41089619_41089620insTTTTTTTTTTTT	GRCh37
NC_000023.9:g.40974563_40974564insTTTTTTTTTTTT	NCBI36
NG_012547.1:g.149732_149733insTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-135_7447-134insTTTTTTTTTTTT	ENSP00000515603.1:n.7447-135_7447-134insTTTTTTTTTTTT
ENST00000703987.1:c.7495-135_7495-134insTTTTTTTTTTTT	ENSP00000515604.1:n.7495-135_7495-134insTTTTTTTTTTTT
ENST00000704649.1:c.3685-2021_3685-2020insTTTTTTTTTTTT	ENSP00000515974.1:n.3685-2021_3685-2020insTTTTTTTTTTTT
ENST00000704650.1:c.7432-135_7432-134insTTTTTTTTTTTT	ENSP00000515975.1:n.7432-135_7432-134insTTTTTTTTTTTT
ENST00000704651.1:c.7279-135_7279-134insTTTTTTTTTTTT	ENSP00000515976.1:n.7279-135_7279-134insTTTTTTTTTTTT
ENST00000704652.1:c.6531-135_6531-134insTTTTTTTTTTTT
ENST00000704654.1:c.4311-135_4311-134insTTTTTTTTTTTT
ENST00000704655.1:c.3575-135_3575-134insTTTTTTTTTTTT	ENSP00000515980.1:n.3575-135_3575-134insTTTTTTTTTTTT
ENST00000704656.1:c.2883-135_2883-134insTTTTTTTTTTTT	ENSP00000515981.1:n.2883-135_2883-134insTTTTTTTTTTTT
ENST00000324545.9:c.7480-135_7480-134insTTTTTTTTTTTT	ENSP00000316357.6:n.7480-135_7480-134insTTTTTTTTTTTT
ENST00000378308.7:c.7432-135_7432-134insTTTTTTTTTTTT MANE Select	ENSP00000367558.2:n.7432-135_7432-134insTTTTTTTTTTTT
ENST00000324545.8:c.7480-135_7480-134insTTTTTTTTTTTT	ENSP00000316357.6:n.7480-135_7480-134insTTTTTTTTTTTT
ENST00000378308.6:c.7432-135_7432-134insTTTTTTTTTTTT	ENSP00000367558.2:n.7432-135_7432-134insTTTTTTTTTTTT
NM_001039590.2:c.7480-135_7480-134insTTTTTTTTTTTT	NP_001034679.2:n.7480-135_7480-134insTTTTTTTTTTTT
NM_001039591.2:c.7432-135_7432-134insTTTTTTTTTTTT	NP_001034680.2:n.7432-135_7432-134insTTTTTTTTTTTT
XM_005272675.3:c.7495-135_7495-134insTTTTTTTTTTTT	XP_005272732.1:n.7495-135_7495-134insTTTTTTTTTTTT
XM_005272676.3:c.7447-135_7447-134insTTTTTTTTTTTT	XP_005272733.1:n.7447-135_7447-134insTTTTTTTTTTTT
XM_005272675.4:c.7495-135_7495-134insTTTTTTTTTTTT	XP_005272732.1:n.7495-135_7495-134insTTTTTTTTTTTT
XM_005272676.4:c.7447-135_7447-134insTTTTTTTTTTTT	XP_005272733.1:n.7447-135_7447-134insTTTTTTTTTTTT
NM_001039591.3:c.7432-135_7432-134insTTTTTTTTTTTT MANE Select	NP_001034680.2:n.7432-135_7432-134insTTTTTTTTTTTT
NM_001039590.3:c.7480-135_7480-134insTTTTTTTTTTTT	NP_001034679.2:n.7480-135_7480-134insTTTTTTTTTTTT