Canonical Allele Identifier: CA2267631352
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273641A= , CM000679.2:g.58273641A= GRCh38
NC_000017.10:g.56351002A= , CM000679.1:g.56351002A= GRCh37
NC_000017.9:g.53706001A= NCBI36
NG_009629.1:g.12295T= , LRG_84:g.12295T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.727T=
ENST00000699291.1:c.519T= ENSP00000514272.1:p.Pro173=
ENST00000699292.1:n.434T=
ENST00000225275.4:c.1394T= MANE Select ENSP00000225275.3:p.Leu465=
ENST00000225275.3:c.1394T= ENSP00000225275.3:p.Leu465=
NM_000250.1:c.1394T= , LRG_84t1:c.1394T= NP_000241.1:p.Leu465=
XM_011524821.1:c.1580T= XP_011523123.1:p.Leu527=
XM_011524822.1:c.1109T= XP_011523124.1:p.Leu370=
XM_011524823.1:c.1419T= XP_011523125.1:p.Pro473=
NM_000250.2:c.1394T= MANE Select NP_000241.1:p.Leu465=