Canonical Allele Identifier: CA412751997

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41088562T>C (hg19) ; chrX:g.41229309T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229309T>C , CM000685.2:g.41229309T>C	GRCh38
NC_000023.10:g.41088562T>C , CM000685.1:g.41088562T>C	GRCh37
NC_000023.9:g.40973506T>C	NCBI36
NG_012547.1:g.148675T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.7133T>C	ENSP00000515603.1:p.Ile2378Thr
ENST00000703987.1:c.7133T>C	ENSP00000515604.1:p.Ile2378Thr
ENST00000704649.1:c.3685-3078T>C	ENSP00000515974.1:n.3685-3078T>C
ENST00000704650.1:c.7118T>C	ENSP00000515975.1:p.Ile2373Thr
ENST00000704651.1:c.6965T>C	ENSP00000515976.1:p.Ile2322Thr
ENST00000704652.1:c.6217T>C
ENST00000704654.1:c.3997T>C
ENST00000704655.1:c.3261T>C	ENSP00000515980.1:n.3261T>C
ENST00000704656.1:c.2569T>C	ENSP00000515981.1:n.2569T>C
ENST00000324545.9:c.7118T>C	ENSP00000316357.6:p.Ile2373Thr
ENST00000378308.7:c.7118T>C MANE Select	ENSP00000367558.2:p.Ile2373Thr
ENST00000324545.8:c.7118T>C	ENSP00000316357.6:p.Ile2373Thr
ENST00000378308.6:c.7118T>C	ENSP00000367558.2:p.Ile2373Thr
ENST00000485180.1:n.327T>C
NM_001039590.2:c.7118T>C	NP_001034679.2:p.Ile2373Thr
NM_001039591.2:c.7118T>C	NP_001034680.2:p.Ile2373Thr
XM_005272675.3:c.7133T>C	XP_005272732.1:p.Ile2378Thr
XM_005272676.3:c.7133T>C	XP_005272733.1:p.Ile2378Thr
XM_005272675.4:c.7133T>C	XP_005272732.1:p.Ile2378Thr
XM_005272676.4:c.7133T>C	XP_005272733.1:p.Ile2378Thr
NM_001039591.3:c.7118T>C MANE Select	NP_001034680.2:p.Ile2373Thr
NM_001039590.3:c.7118T>C	NP_001034679.2:p.Ile2373Thr