Canonical Allele Identifier: CA396974093

Gene: USP10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84745647A>C , CM000678.2:g.84745647A>C	GRCh38
NC_000016.9:g.84779253A>C , CM000678.1:g.84779253A>C	GRCh37
NC_000016.8:g.83336754A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005153.3:c.1166A>C MANE Select	NP_005144.2:p.Glu389Ala
ENST00000219473.12:c.1166A>C MANE Select	ENSP00000219473.7:p.Glu389Ala
NM_001272075.1:c.1178A>C	NP_001259004.1:p.Glu393Ala
NM_001272075.2:c.1178A>C	NP_001259004.1:p.Glu393Ala
NM_005153.2:c.1166A>C	NP_005144.2:p.Glu389Ala
NR_073577.1:n.232+12144A>C
NR_073577.2:n.181+12144A>C
NR_073578.1:n.1247A>C
NR_073578.2:n.1196A>C
ENST00000219473.11:c.1166A>C	ENSP00000219473.7:p.Glu389Ala
ENST00000540269.6:c.*916A>C	ENSP00000445589.2:n.*916A>C
ENST00000563048.5:c.90+12144A>C	ENSP00000454902.1:n.90+12144A>C
ENST00000563892.5:c.151+5278A>C	ENSP00000458089.1:n.151+5278A>C
ENST00000569038.5:c.41A>C	ENSP00000462762.1:p.Glu14Ala
ENST00000570053.1:c.90+12144A>C	ENSP00000454751.1:n.90+12144A>C
ENST00000570191.5:c.1178A>C	ENSP00000457411.1:p.Glu393Ala
XM_006721330.1:c.1181A>C	XP_006721393.1:p.Glu394Ala
XM_006721331.1:c.1181A>C	XP_006721394.1:p.Glu394Ala
XM_006721332.1:c.578A>C	XP_006721395.1:p.Glu193Ala
XM_011523440.1:c.578A>C	XP_011521742.1:p.Glu193Ala
XM_011523441.1:c.578A>C	XP_011521743.1:p.Glu193Ala
XM_011523442.1:c.578A>C	XP_011521744.1:p.Glu193Ala
XM_011523443.1:c.578A>C	XP_011521745.1:p.Glu193Ala
XM_017023863.1:c.578A>C	XP_016879352.1:p.Glu193Ala
XM_017023864.1:c.578A>C	XP_016879353.1:p.Glu193Ala
XM_017023865.1:c.578A>C	XP_016879354.1:p.Glu193Ala
XM_017023866.2:c.578A>C	XP_016879355.1:p.Glu193Ala
XM_017023867.1:c.578A>C	XP_016879356.1:p.Glu193Ala
XM_017023868.1:c.578A>C	XP_016879357.1:p.Glu193Ala
XM_017023869.1:c.578A>C	XP_016879358.1:p.Glu193Ala