Canonical Allele Identifier: CA8210460

Gene: USP10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84733469A>G , CM000678.2:g.84733469A>G	GRCh38
NC_000016.9:g.84767075A>G , CM000678.1:g.84767075A>G	GRCh37
NC_000016.8:g.83324576A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219473.12:c.56A>G MANE Select	ENSP00000219473.7:p.Asn19Ser
ENST00000219473.11:c.56A>G	ENSP00000219473.7:p.Asn19Ser
ENST00000540269.6:c.56A>G	ENSP00000445589.2:p.Asn19Ser
ENST00000562092.1:n.216A>G
ENST00000562283.5:c.38A>G	ENSP00000455712.1:p.Asn13Ser
ENST00000562743.5:n.214A>G
ENST00000563023.1:n.261A>G
ENST00000563048.5:c.56A>G	ENSP00000454902.1:p.Asn19Ser
ENST00000563386.5:c.178A>G	ENSP00000454943.1:p.Ile60Val
ENST00000563892.5:c.56A>G	ENSP00000458089.1:p.Asn19Ser
ENST00000566512.1:n.332A>G
ENST00000569038.5:c.6+388A>G	ENSP00000462762.1:n.6+388A>G
ENST00000570053.1:c.56A>G	ENSP00000454751.1:p.Asn19Ser
ENST00000570191.5:c.68A>G	ENSP00000457411.1:p.Asn23Ser
NM_001272075.1:c.68A>G	NP_001259004.1:p.Asn23Ser
NM_005153.2:c.56A>G	NP_005144.2:p.Asn19Ser
NR_073577.1:n.198A>G
NR_073578.1:n.198A>G
XM_006721330.1:c.71A>G	XP_006721393.1:p.Asn24Ser
XM_006721331.1:c.71A>G	XP_006721394.1:p.Asn24Ser
XM_006721332.1:c.-533A>G	XP_006721395.1:n.-533A>G
XM_011523440.1:c.-533A>G	XP_011521742.1:n.-533A>G
XM_011523441.1:c.-533A>G	XP_011521743.1:n.-533A>G
XM_011523442.1:c.-533A>G	XP_011521744.1:n.-533A>G
XM_011523443.1:c.-533A>G	XP_011521745.1:n.-533A>G
XM_017023863.1:c.-533A>G	XP_016879352.1:n.-533A>G
XM_017023864.1:c.-533A>G	XP_016879353.1:n.-533A>G
XM_017023865.1:c.-533A>G	XP_016879354.1:n.-533A>G
XM_017023866.2:c.-533A>G	XP_016879355.1:n.-533A>G
XM_017023867.1:c.-533A>G	XP_016879356.1:n.-533A>G
XM_017023868.1:c.-533A>G	XP_016879357.1:n.-533A>G
XM_017023869.1:c.-533A>G	XP_016879358.1:n.-533A>G
NM_001272075.2:c.68A>G	NP_001259004.1:p.Asn23Ser
NM_005153.3:c.56A>G MANE Select	NP_005144.2:p.Asn19Ser
NR_073577.2:n.147A>G
NR_073578.2:n.147A>G