Canonical Allele Identifier: CA8686205

Gene: USP32

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60214663C>T , CM000679.2:g.60214663C>T	GRCh38
NC_000017.10:g.58292024C>T , CM000679.1:g.58292024C>T	GRCh37
NC_000017.9:g.55646806C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300896.9:c.1979G>A MANE Select	ENSP00000300896.3:p.Arg660His
ENST00000300896.8:c.1979G>A	ENSP00000300896.3:p.Arg660His
ENST00000590133.5:c.1970G>A	ENSP00000465844.1:p.Arg657His
ENST00000591768.1:c.614G>A	ENSP00000464762.1:p.Arg205His
ENST00000592339.5:c.989G>A	ENSP00000467885.1:p.Arg330His
NM_032582.3:c.1979G>A	NP_115971.2:p.Arg660His
XM_011525371.1:c.2069G>A	XP_011523673.1:p.Arg690His
XM_011525372.1:c.2027G>A	XP_011523674.1:p.Arg676His
XM_011525373.1:c.2021G>A	XP_011523675.1:p.Arg674His
XM_011525374.1:c.2012G>A	XP_011523676.1:p.Arg671His
XM_011525375.1:c.1991G>A	XP_011523677.1:p.Arg664His
XM_011525376.1:c.1970G>A	XP_011523678.1:p.Arg657His
XM_011525377.1:c.1937G>A	XP_011523679.1:p.Arg646His
XM_011525378.1:c.1883G>A	XP_011523680.1:p.Arg628His
XM_011525379.1:c.1148G>A	XP_011523681.1:p.Arg383His
XM_011525379.3:c.1148G>A	XP_011523681.1:p.Arg383His
XM_017025233.1:c.1841G>A	XP_016880722.1:p.Arg614His
XM_017025234.1:c.1031G>A	XP_016880723.1:p.Arg344His
NM_032582.4:c.1979G>A MANE Select	NP_115971.2:p.Arg660His