Canonical Allele Identifier: CA2693481439

Gene: USP9X

Linked Data

• gnomAD v4: X-41230364-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230364G>C , CM000685.2:g.41230364G>C	GRCh38
NC_000023.10:g.41089617G>C , CM000685.1:g.41089617G>C	GRCh37
NC_000023.9:g.40974561G>C	NCBI36
NG_012547.1:g.149730G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-137G>C	ENSP00000515603.1:n.7447-137G>C
ENST00000703987.1:c.7495-137G>C	ENSP00000515604.1:n.7495-137G>C
ENST00000704649.1:c.3685-2023G>C	ENSP00000515974.1:n.3685-2023G>C
ENST00000704650.1:c.7432-137G>C	ENSP00000515975.1:n.7432-137G>C
ENST00000704651.1:c.7279-137G>C	ENSP00000515976.1:n.7279-137G>C
ENST00000704652.1:c.6531-137G>C
ENST00000704654.1:c.4311-137G>C
ENST00000704655.1:c.3575-137G>C	ENSP00000515980.1:n.3575-137G>C
ENST00000704656.1:c.2883-137G>C	ENSP00000515981.1:n.2883-137G>C
ENST00000324545.9:c.7480-137G>C	ENSP00000316357.6:n.7480-137G>C
ENST00000378308.7:c.7432-137G>C MANE Select	ENSP00000367558.2:n.7432-137G>C
ENST00000324545.8:c.7480-137G>C	ENSP00000316357.6:n.7480-137G>C
ENST00000378308.6:c.7432-137G>C	ENSP00000367558.2:n.7432-137G>C
NM_001039590.2:c.7480-137G>C	NP_001034679.2:n.7480-137G>C
NM_001039591.2:c.7432-137G>C	NP_001034680.2:n.7432-137G>C
XM_005272675.3:c.7495-137G>C	XP_005272732.1:n.7495-137G>C
XM_005272676.3:c.7447-137G>C	XP_005272733.1:n.7447-137G>C
XM_005272675.4:c.7495-137G>C	XP_005272732.1:n.7495-137G>C
XM_005272676.4:c.7447-137G>C	XP_005272733.1:n.7447-137G>C
NM_001039591.3:c.7432-137G>C MANE Select	NP_001034680.2:n.7432-137G>C
NM_001039590.3:c.7480-137G>C	NP_001034679.2:n.7480-137G>C