Canonical Allele Identifier: CA2267631317

Gene: MPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273562_58273567delinsGGCGAT , CM000679.2:g.58273562_58273567delinsGGCGAT	GRCh38
NC_000017.10:g.56350923_56350928delinsGGCGAT , CM000679.1:g.56350923_56350928delinsGGCGAT	GRCh37
NC_000017.9:g.53705922_53705927delinsGGCGAT	NCBI36
NG_009629.1:g.12369_12374delinsATCGCC , LRG_84:g.12369_12374delinsATCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.801_806delinsATCGCC
ENST00000699291.1:c.593_598delinsATCGCC	ENSP00000514272.1:n.593_598delinsATCGCC
ENST00000699292.1:n.508_513delinsATCGCC
ENST00000225275.4:c.1468_1473delinsATCGCC MANE Select	ENSP00000225275.3:p.Ile490=
ENST00000225275.3:c.1468_1473delinsATCGCC	ENSP00000225275.3:p.Ile490=
NM_000250.1:c.1468_1473delinsATCGCC , LRG_84t1:c.1468_1473delinsATCGCC	NP_000241.1:p.Ile490=
XM_011524821.1:c.1654_1659delinsATCGCC	XP_011523123.1:p.Ile552=
XM_011524822.1:c.1183_1188delinsATCGCC	XP_011523124.1:p.Ile395=
XM_011524823.1:c.*17_*22delinsATCGCC	XP_011523125.1:n.*17_*22delinsATCGCC
NM_000250.2:c.1468_1473delinsATCGCC MANE Select	NP_000241.1:p.Ile490=