Canonical Allele Identifier: CA2267631290
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273511G= , CM000679.2:g.58273511G= GRCh38
NC_000017.10:g.56350872G= , CM000679.1:g.56350872G= GRCh37
NC_000017.9:g.53705871G= NCBI36
NG_009629.1:g.12425C= , LRG_84:g.12425C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.857C=
ENST00000699291.1:c.649C= ENSP00000514272.1:n.649C=
ENST00000699292.1:n.564C=
ENST00000225275.4:c.1524C= MANE Select ENSP00000225275.3:p.Phe508=
ENST00000225275.3:c.1524C= ENSP00000225275.3:p.Phe508=
NM_000250.1:c.1524C= , LRG_84t1:c.1524C= NP_000241.1:p.Phe508=
XM_011524821.1:c.1710C= XP_011523123.1:p.Phe570=
XM_011524822.1:c.1239C= XP_011523124.1:p.Phe413=
XM_011524823.1:c.*73C= XP_011523125.1:n.*73C=
NM_000250.2:c.1524C= MANE Select NP_000241.1:p.Phe508=