Canonical Allele Identifier: CA2741065

Gene: SENP2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185613377C>A , CM000665.2:g.185613377C>A	GRCh38
NC_000003.11:g.185331165C>A , CM000665.1:g.185331165C>A	GRCh37
NC_000003.10:g.186813859C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296257.10:c.902C>A MANE Select	ENSP00000296257.5:p.Thr301Lys
ENST00000296257.9:c.902C>A	ENSP00000296257.5:p.Thr301Lys
ENST00000413407.5:c.*520C>A	ENSP00000388893.1:n.*520C>A
ENST00000444509.1:c.23C>A	ENSP00000399201.1:p.Thr8Lys
ENST00000473760.5:n.604C>A
ENST00000476011.1:n.470C>A
ENST00000478001.1:n.303C>A
NM_021627.2:c.902C>A	NP_067640.2:p.Thr301Lys
XM_005247690.2:c.902C>A	XP_005247747.2:p.Thr301Lys
XM_005247691.1:c.557C>A	XP_005247748.1:p.Thr186Lys
XM_005247690.3:c.902C>A	XP_005247747.2:p.Thr301Lys
XM_005247691.3:c.557C>A	XP_005247748.1:p.Thr186Lys
XM_017006973.2:c.557C>A	XP_016862462.1:p.Thr186Lys
NM_021627.3:c.902C>A MANE Select	NP_067640.2:p.Thr301Lys