Canonical Allele Identifier: CA10388642

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41171831A>G , CM000685.2:g.41171831A>G	GRCh38
NC_000023.10:g.41031084A>G , CM000685.1:g.41031084A>G	GRCh37
NC_000023.9:g.40916028A>G	NCBI36
NG_012547.1:g.91197A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.3028-7A>G MANE Select	NP_001034680.2:n.3028-7A>G
ENST00000378308.7:c.3028-7A>G MANE Select	ENSP00000367558.2:n.3028-7A>G
NM_001039590.2:c.3028-7A>G	NP_001034679.2:n.3028-7A>G
NM_001039590.3:c.3028-7A>G	NP_001034679.2:n.3028-7A>G
NM_001039591.2:c.3028-7A>G	NP_001034680.2:n.3028-7A>G
ENST00000324545.8:c.3028-7A>G	ENSP00000316357.6:n.3028-7A>G
ENST00000324545.9:c.3028-7A>G	ENSP00000316357.6:n.3028-7A>G
ENST00000378308.6:c.3028-7A>G	ENSP00000367558.2:n.3028-7A>G
ENST00000703986.1:c.3043-7A>G	ENSP00000515603.1:n.3043-7A>G
ENST00000703987.1:c.3043-7A>G	ENSP00000515604.1:n.3043-7A>G
ENST00000704649.1:c.3028-7A>G	ENSP00000515974.1:n.3028-7A>G
ENST00000704650.1:c.3028-7A>G	ENSP00000515975.1:n.3028-7A>G
ENST00000704651.1:c.2875-7A>G	ENSP00000515976.1:n.2875-7A>G
ENST00000704652.1:c.2258-7A>G
XM_005272675.3:c.3043-7A>G	XP_005272732.1:n.3043-7A>G
XM_005272675.4:c.3043-7A>G	XP_005272732.1:n.3043-7A>G
XM_005272676.3:c.3043-7A>G	XP_005272733.1:n.3043-7A>G
XM_005272676.4:c.3043-7A>G	XP_005272733.1:n.3043-7A>G