Canonical Allele Identifier: CA8210693

Gene: USP10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84745301G>A , CM000678.2:g.84745301G>A	GRCh38
NC_000016.9:g.84778907G>A , CM000678.1:g.84778907G>A	GRCh37
NC_000016.8:g.83336408G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219473.12:c.820G>A MANE Select	ENSP00000219473.7:p.Val274Ile
ENST00000219473.11:c.820G>A	ENSP00000219473.7:p.Val274Ile
ENST00000540269.6:c.*570G>A	ENSP00000445589.2:n.*570G>A
ENST00000563048.5:c.90+11798G>A	ENSP00000454902.1:n.90+11798G>A
ENST00000563892.5:c.151+4932G>A	ENSP00000458089.1:n.151+4932G>A
ENST00000569038.5:c.7-312G>A	ENSP00000462762.1:n.7-312G>A
ENST00000570053.1:c.90+11798G>A	ENSP00000454751.1:n.90+11798G>A
ENST00000570191.5:c.832G>A	ENSP00000457411.1:p.Val278Ile
NM_001272075.1:c.832G>A	NP_001259004.1:p.Val278Ile
NM_005153.2:c.820G>A	NP_005144.2:p.Val274Ile
NR_073577.1:n.232+11798G>A
NR_073578.1:n.901G>A
XM_006721330.1:c.835G>A	XP_006721393.1:p.Val279Ile
XM_006721331.1:c.835G>A	XP_006721394.1:p.Val279Ile
XM_006721332.1:c.232G>A	XP_006721395.1:p.Val78Ile
XM_011523440.1:c.232G>A	XP_011521742.1:p.Val78Ile
XM_011523441.1:c.232G>A	XP_011521743.1:p.Val78Ile
XM_011523442.1:c.232G>A	XP_011521744.1:p.Val78Ile
XM_011523443.1:c.232G>A	XP_011521745.1:p.Val78Ile
XM_017023863.1:c.232G>A	XP_016879352.1:p.Val78Ile
XM_017023864.1:c.232G>A	XP_016879353.1:p.Val78Ile
XM_017023865.1:c.232G>A	XP_016879354.1:p.Val78Ile
XM_017023866.2:c.232G>A	XP_016879355.1:p.Val78Ile
XM_017023867.1:c.232G>A	XP_016879356.1:p.Val78Ile
XM_017023868.1:c.232G>A	XP_016879357.1:p.Val78Ile
XM_017023869.1:c.232G>A	XP_016879358.1:p.Val78Ile
NM_001272075.2:c.832G>A	NP_001259004.1:p.Val278Ile
NM_005153.3:c.820G>A MANE Select	NP_005144.2:p.Val274Ile
NR_073577.2:n.181+11798G>A
NR_073578.2:n.850G>A