Canonical Allele Identifier: CA412768204

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41141351G>A , CM000685.2:g.41141351G>A	GRCh38
NC_000023.10:g.41000604G>A , CM000685.1:g.41000604G>A	GRCh37
NC_000023.9:g.40885548G>A	NCBI36
NG_012547.1:g.60717G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.1081G>A MANE Select	NP_001034680.2:p.Val361Met
ENST00000378308.7:c.1081G>A MANE Select	ENSP00000367558.2:p.Val361Met
NM_001039590.2:c.1081G>A	NP_001034679.2:p.Val361Met
NM_001039590.3:c.1081G>A	NP_001034679.2:p.Val361Met
NM_001039591.2:c.1081G>A	NP_001034680.2:p.Val361Met
ENST00000324545.8:c.1081G>A	ENSP00000316357.6:p.Val361Met
ENST00000324545.9:c.1081G>A	ENSP00000316357.6:p.Val361Met
ENST00000378308.6:c.1081G>A	ENSP00000367558.2:p.Val361Met
ENST00000703986.1:c.1081G>A	ENSP00000515603.1:p.Val361Met
ENST00000703987.1:c.1081G>A	ENSP00000515604.1:p.Val361Met
ENST00000704649.1:c.1081G>A	ENSP00000515974.1:p.Val361Met
ENST00000704650.1:c.1081G>A	ENSP00000515975.1:p.Val361Met
ENST00000704651.1:c.1081G>A	ENSP00000515976.1:p.Val361Met
ENST00000704652.1:c.311G>A
XM_005272675.3:c.1081G>A	XP_005272732.1:p.Val361Met
XM_005272675.4:c.1081G>A	XP_005272732.1:p.Val361Met
XM_005272676.3:c.1081G>A	XP_005272733.1:p.Val361Met
XM_005272676.4:c.1081G>A	XP_005272733.1:p.Val361Met