Canonical Allele Identifier: CA412763104

Gene: USP9X

Linked Data

• dbSNP Id: rs1191790572
• gnomAD v2: X-40996148-T-C
• gnomAD v4: X-41136895-T-C
• MyVariant Identifiers: chrX:g.40996148T>C (hg19) ; chrX:g.41136895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41136895T>C , CM000685.2:g.41136895T>C	GRCh38
NC_000023.10:g.40996148T>C , CM000685.1:g.40996148T>C	GRCh37
NC_000023.9:g.40881092T>C	NCBI36
NG_012547.1:g.56261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.527T>C	ENSP00000515603.1:p.Met176Thr
ENST00000703987.1:c.527T>C	ENSP00000515604.1:p.Met176Thr
ENST00000704649.1:c.527T>C	ENSP00000515974.1:p.Met176Thr
ENST00000704650.1:c.527T>C	ENSP00000515975.1:p.Met176Thr
ENST00000704651.1:c.527T>C	ENSP00000515976.1:p.Met176Thr
ENST00000324545.9:c.527T>C	ENSP00000316357.6:p.Met176Thr
ENST00000378308.7:c.527T>C MANE Select	ENSP00000367558.2:p.Met176Thr
ENST00000324545.8:c.527T>C	ENSP00000316357.6:p.Met176Thr
ENST00000378308.6:c.527T>C	ENSP00000367558.2:p.Met176Thr
NM_001039590.2:c.527T>C	NP_001034679.2:p.Met176Thr
NM_001039591.2:c.527T>C	NP_001034680.2:p.Met176Thr
XM_005272675.3:c.527T>C	XP_005272732.1:p.Met176Thr
XM_005272676.3:c.527T>C	XP_005272733.1:p.Met176Thr
XM_005272675.4:c.527T>C	XP_005272732.1:p.Met176Thr
XM_005272676.4:c.527T>C	XP_005272733.1:p.Met176Thr
NM_001039591.3:c.527T>C MANE Select	NP_001034680.2:p.Met176Thr
NM_001039590.3:c.527T>C	NP_001034679.2:p.Met176Thr