Canonical Allele Identifier: CA412754746

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41089849G>C (hg19) ; chrX:g.41230596G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230596G>C , CM000685.2:g.41230596G>C	GRCh38
NC_000023.10:g.41089849G>C , CM000685.1:g.41089849G>C	GRCh37
NC_000023.9:g.40974793G>C	NCBI36
NG_012547.1:g.149962G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7542G>C	ENSP00000515603.1:p.Gln2514His
ENST00000703987.1:c.7590G>C	ENSP00000515604.1:p.Gln2530His
ENST00000704649.1:c.3685-1791G>C	ENSP00000515974.1:n.3685-1791G>C
ENST00000704650.1:c.7527G>C	ENSP00000515975.1:p.Gln2509His
ENST00000704651.1:c.7374G>C	ENSP00000515976.1:p.Gln2458His
ENST00000704652.1:c.6626G>C
ENST00000704654.1:c.4406G>C
ENST00000704655.1:c.3670G>C	ENSP00000515980.1:n.3670G>C
ENST00000704656.1:c.2978G>C	ENSP00000515981.1:n.2978G>C
ENST00000324545.9:c.7575G>C	ENSP00000316357.6:p.Gln2525His
ENST00000378308.7:c.7527G>C MANE Select	ENSP00000367558.2:p.Gln2509His
ENST00000324545.8:c.7575G>C	ENSP00000316357.6:p.Gln2525His
ENST00000378308.6:c.7527G>C	ENSP00000367558.2:p.Gln2509His
NM_001039590.2:c.7575G>C	NP_001034679.2:p.Gln2525His
NM_001039591.2:c.7527G>C	NP_001034680.2:p.Gln2509His
XM_005272675.3:c.7590G>C	XP_005272732.1:p.Gln2530His
XM_005272676.3:c.7542G>C	XP_005272733.1:p.Gln2514His
XM_005272675.4:c.7590G>C	XP_005272732.1:p.Gln2530His
XM_005272676.4:c.7542G>C	XP_005272733.1:p.Gln2514His
NM_001039591.3:c.7527G>C MANE Select	NP_001034680.2:p.Gln2509His
NM_001039590.3:c.7575G>C	NP_001034679.2:p.Gln2525His