Canonical Allele Identifier: CA2267631336
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273602G= , CM000679.2:g.58273602G= GRCh38
NC_000017.10:g.56350963G= , CM000679.1:g.56350963G= GRCh37
NC_000017.9:g.53705962G= NCBI36
NG_009629.1:g.12334C= , LRG_84:g.12334C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.766C=
ENST00000699291.1:c.558C= ENSP00000514272.1:p.His186=
ENST00000699292.1:n.473C=
ENST00000225275.4:c.1433C= MANE Select ENSP00000225275.3:p.Thr478=
ENST00000225275.3:c.1433C= ENSP00000225275.3:p.Thr478=
NM_000250.1:c.1433C= , LRG_84t1:c.1433C= NP_000241.1:p.Thr478=
XM_011524821.1:c.1619C= XP_011523123.1:p.Thr540=
XM_011524822.1:c.1148C= XP_011523124.1:p.Thr383=
XM_011524823.1:c.1458C= XP_011523125.1:p.His486=
NM_000250.2:c.1433C= MANE Select NP_000241.1:p.Thr478=