Canonical Allele Identifier: CA8686382

Gene: USP32

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60226111C>T , CM000679.2:g.60226111C>T	GRCh38
NC_000017.10:g.58303472C>T , CM000679.1:g.58303472C>T	GRCh37
NC_000017.9:g.55658254C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300896.9:c.1360G>A MANE Select	ENSP00000300896.3:p.Val454Met
ENST00000300896.8:c.1360G>A	ENSP00000300896.3:p.Val454Met
ENST00000587651.1:n.39G>A
ENST00000589552.1:c.121G>A	ENSP00000465922.1:p.Val41Met
ENST00000590133.5:c.1351G>A	ENSP00000465844.1:p.Val451Met
ENST00000592339.5:c.370G>A	ENSP00000467885.1:p.Val124Met
NM_032582.3:c.1360G>A	NP_115971.2:p.Val454Met
XM_011525371.1:c.1408G>A	XP_011523673.1:p.Val470Met
XM_011525372.1:c.1408G>A	XP_011523674.1:p.Val470Met
XM_011525373.1:c.1360G>A	XP_011523675.1:p.Val454Met
XM_011525374.1:c.1351G>A	XP_011523676.1:p.Val451Met
XM_011525375.1:c.1330G>A	XP_011523677.1:p.Val444Met
XM_011525376.1:c.1351G>A	XP_011523678.1:p.Val451Met
XM_011525377.1:c.1276G>A	XP_011523679.1:p.Val426Met
XM_011525378.1:c.1222G>A	XP_011523680.1:p.Val408Met
XM_011525379.1:c.487G>A	XP_011523681.1:p.Val163Met
XM_011525379.3:c.487G>A	XP_011523681.1:p.Val163Met
XM_017025233.1:c.1222G>A	XP_016880722.1:p.Val408Met
XM_017025234.1:c.370G>A	XP_016880723.1:p.Val124Met
NM_032582.4:c.1360G>A MANE Select	NP_115971.2:p.Val454Met