Canonical Allele Identifier: CA412751838

Gene: USP9X

Linked Data

• gnomAD v4: X-41229263-G-T
• COSMIC: COSM6260398 ; COSM6260399
• MyVariant Identifiers: chrX:g.41088516G>T (hg19) ; chrX:g.41229263G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229263G>T , CM000685.2:g.41229263G>T	GRCh38
NC_000023.10:g.41088516G>T , CM000685.1:g.41088516G>T	GRCh37
NC_000023.9:g.40973460G>T	NCBI36
NG_012547.1:g.148629G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7087G>T	ENSP00000515603.1:p.Ala2363Ser
ENST00000703987.1:c.7087G>T	ENSP00000515604.1:p.Ala2363Ser
ENST00000704649.1:c.3685-3124G>T	ENSP00000515974.1:n.3685-3124G>T
ENST00000704650.1:c.7072G>T	ENSP00000515975.1:p.Ala2358Ser
ENST00000704651.1:c.6919G>T	ENSP00000515976.1:p.Ala2307Ser
ENST00000704652.1:c.6171G>T
ENST00000704654.1:c.3951G>T
ENST00000704655.1:c.3215G>T	ENSP00000515980.1:n.3215G>T
ENST00000704656.1:c.2523G>T	ENSP00000515981.1:n.2523G>T
ENST00000324545.9:c.7072G>T	ENSP00000316357.6:p.Ala2358Ser
ENST00000378308.7:c.7072G>T MANE Select	ENSP00000367558.2:p.Ala2358Ser
ENST00000324545.8:c.7072G>T	ENSP00000316357.6:p.Ala2358Ser
ENST00000378308.6:c.7072G>T	ENSP00000367558.2:p.Ala2358Ser
ENST00000485180.1:n.281G>T
NM_001039590.2:c.7072G>T	NP_001034679.2:p.Ala2358Ser
NM_001039591.2:c.7072G>T	NP_001034680.2:p.Ala2358Ser
XM_005272675.3:c.7087G>T	XP_005272732.1:p.Ala2363Ser
XM_005272676.3:c.7087G>T	XP_005272733.1:p.Ala2363Ser
XM_005272675.4:c.7087G>T	XP_005272732.1:p.Ala2363Ser
XM_005272676.4:c.7087G>T	XP_005272733.1:p.Ala2363Ser
NM_001039591.3:c.7072G>T MANE Select	NP_001034680.2:p.Ala2358Ser
NM_001039590.3:c.7072G>T	NP_001034679.2:p.Ala2358Ser