Canonical Allele Identifier: CA396970687

Gene: USP10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84744681C>A , CM000678.2:g.84744681C>A	GRCh38
NC_000016.9:g.84778287C>A , CM000678.1:g.84778287C>A	GRCh37
NC_000016.8:g.83335788C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219473.12:c.200C>A MANE Select	ENSP00000219473.7:p.Pro67His
ENST00000219473.11:c.200C>A	ENSP00000219473.7:p.Pro67His
ENST00000540269.6:c.139C>A	ENSP00000445589.2:p.Pro47Thr
ENST00000562283.5:c.182C>A	ENSP00000455712.1:p.Pro61His
ENST00000562743.5:n.358C>A
ENST00000563023.1:n.344C>A
ENST00000563048.5:c.90+11178C>A	ENSP00000454902.1:n.90+11178C>A
ENST00000563386.5:c.*130C>A	ENSP00000454943.1:n.*130C>A
ENST00000563892.5:c.151+4312C>A	ENSP00000458089.1:n.151+4312C>A
ENST00000566512.1:n.476C>A
ENST00000569038.5:c.7-932C>A	ENSP00000462762.1:n.7-932C>A
ENST00000570053.1:c.90+11178C>A	ENSP00000454751.1:n.90+11178C>A
ENST00000570191.5:c.212C>A	ENSP00000457411.1:p.Pro71His
NM_001272075.1:c.212C>A	NP_001259004.1:p.Pro71His
NM_005153.2:c.200C>A	NP_005144.2:p.Pro67His
NR_073577.1:n.232+11178C>A
NR_073578.1:n.281C>A
XM_006721330.1:c.215C>A	XP_006721393.1:p.Pro72His
XM_006721331.1:c.215C>A	XP_006721394.1:p.Pro72His
XM_006721332.1:c.-389C>A	XP_006721395.1:n.-389C>A
XM_011523440.1:c.-389C>A	XP_011521742.1:n.-389C>A
XM_011523441.1:c.-389C>A	XP_011521743.1:n.-389C>A
XM_011523442.1:c.-389C>A	XP_011521744.1:n.-389C>A
XM_011523443.1:c.-389C>A	XP_011521745.1:n.-389C>A
XM_017023863.1:c.-389C>A	XP_016879352.1:n.-389C>A
XM_017023864.1:c.-389C>A	XP_016879353.1:n.-389C>A
XM_017023865.1:c.-389C>A	XP_016879354.1:n.-389C>A
XM_017023866.2:c.-389C>A	XP_016879355.1:n.-389C>A
XM_017023867.1:c.-389C>A	XP_016879356.1:n.-389C>A
XM_017023868.1:c.-389C>A	XP_016879357.1:n.-389C>A
XM_017023869.1:c.-389C>A	XP_016879358.1:n.-389C>A
NM_001272075.2:c.212C>A	NP_001259004.1:p.Pro71His
NM_005153.3:c.200C>A MANE Select	NP_005144.2:p.Pro67His
NR_073577.2:n.181+11178C>A
NR_073578.2:n.230C>A