Canonical Allele Identifier: CA396973352

Gene: USP10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84745388G>C , CM000678.2:g.84745388G>C	GRCh38
NC_000016.9:g.84778994G>C , CM000678.1:g.84778994G>C	GRCh37
NC_000016.8:g.83336495G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219473.12:c.907G>C MANE Select	ENSP00000219473.7:p.Glu303Gln
ENST00000219473.11:c.907G>C	ENSP00000219473.7:p.Glu303Gln
ENST00000540269.6:c.*657G>C	ENSP00000445589.2:n.*657G>C
ENST00000563048.5:c.90+11885G>C	ENSP00000454902.1:n.90+11885G>C
ENST00000563892.5:c.151+5019G>C	ENSP00000458089.1:n.151+5019G>C
ENST00000569038.5:c.7-225G>C	ENSP00000462762.1:n.7-225G>C
ENST00000570053.1:c.90+11885G>C	ENSP00000454751.1:n.90+11885G>C
ENST00000570191.5:c.919G>C	ENSP00000457411.1:p.Glu307Gln
NM_001272075.1:c.919G>C	NP_001259004.1:p.Glu307Gln
NM_005153.2:c.907G>C	NP_005144.2:p.Glu303Gln
NR_073577.1:n.232+11885G>C
NR_073578.1:n.988G>C
XM_006721330.1:c.922G>C	XP_006721393.1:p.Glu308Gln
XM_006721331.1:c.922G>C	XP_006721394.1:p.Glu308Gln
XM_006721332.1:c.319G>C	XP_006721395.1:p.Glu107Gln
XM_011523440.1:c.319G>C	XP_011521742.1:p.Glu107Gln
XM_011523441.1:c.319G>C	XP_011521743.1:p.Glu107Gln
XM_011523442.1:c.319G>C	XP_011521744.1:p.Glu107Gln
XM_011523443.1:c.319G>C	XP_011521745.1:p.Glu107Gln
XM_017023863.1:c.319G>C	XP_016879352.1:p.Glu107Gln
XM_017023864.1:c.319G>C	XP_016879353.1:p.Glu107Gln
XM_017023865.1:c.319G>C	XP_016879354.1:p.Glu107Gln
XM_017023866.2:c.319G>C	XP_016879355.1:p.Glu107Gln
XM_017023867.1:c.319G>C	XP_016879356.1:p.Glu107Gln
XM_017023868.1:c.319G>C	XP_016879357.1:p.Glu107Gln
XM_017023869.1:c.319G>C	XP_016879358.1:p.Glu107Gln
NM_001272075.2:c.919G>C	NP_001259004.1:p.Glu307Gln
NM_005153.3:c.907G>C MANE Select	NP_005144.2:p.Glu303Gln
NR_073577.2:n.181+11885G>C
NR_073578.2:n.937G>C