Canonical Allele Identifier: CA515960766

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41089795T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230542T>C , CM000685.2:g.41230542T>C	GRCh38
NC_000023.10:g.41089795T>C , CM000685.1:g.41089795T>C	GRCh37
NC_000023.9:g.40974739T>C	NCBI36
NG_012547.1:g.149908T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7488T>C	ENSP00000515603.1:p.Pro2496=
ENST00000703987.1:c.7536T>C	ENSP00000515604.1:p.Pro2512=
ENST00000704649.1:c.3685-1845T>C	ENSP00000515974.1:n.3685-1845T>C
ENST00000704650.1:c.7473T>C	ENSP00000515975.1:p.Pro2491=
ENST00000704651.1:c.7320T>C	ENSP00000515976.1:p.Pro2440=
ENST00000704652.1:c.6572T>C
ENST00000704654.1:c.4352T>C
ENST00000704655.1:c.3616T>C	ENSP00000515980.1:n.3616T>C
ENST00000704656.1:c.2924T>C	ENSP00000515981.1:n.2924T>C
ENST00000324545.9:c.7521T>C	ENSP00000316357.6:p.Pro2507=
ENST00000378308.7:c.7473T>C MANE Select	ENSP00000367558.2:p.Pro2491=
ENST00000324545.8:c.7521T>C	ENSP00000316357.6:p.Pro2507=
ENST00000378308.6:c.7473T>C	ENSP00000367558.2:p.Pro2491=
NM_001039590.2:c.7521T>C	NP_001034679.2:p.Pro2507=
NM_001039591.2:c.7473T>C	NP_001034680.2:p.Pro2491=
XM_005272675.3:c.7536T>C	XP_005272732.1:p.Pro2512=
XM_005272676.3:c.7488T>C	XP_005272733.1:p.Pro2496=
XM_005272675.4:c.7536T>C	XP_005272732.1:p.Pro2512=
XM_005272676.4:c.7488T>C	XP_005272733.1:p.Pro2496=
NM_001039591.3:c.7473T>C MANE Select	NP_001034680.2:p.Pro2491=
NM_001039590.3:c.7521T>C	NP_001034679.2:p.Pro2507=