Canonical Allele Identifier: CA2267631308
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273549T= , CM000679.2:g.58273549T= GRCh38
NC_000017.10:g.56350910T= , CM000679.1:g.56350910T= GRCh37
NC_000017.9:g.53705909T= NCBI36
NG_009629.1:g.12387A= , LRG_84:g.12387A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.819A=
ENST00000699291.1:c.611A= ENSP00000514272.1:n.611A=
ENST00000699292.1:n.526A=
ENST00000225275.4:c.1486A= MANE Select ENSP00000225275.3:p.Asn496=
ENST00000225275.3:c.1486A= ENSP00000225275.3:p.Asn496=
NM_000250.1:c.1486A= , LRG_84t1:c.1486A= NP_000241.1:p.Asn496=
XM_011524821.1:c.1672A= XP_011523123.1:p.Asn558=
XM_011524822.1:c.1201A= XP_011523124.1:p.Asn401=
XM_011524823.1:c.*35A= XP_011523125.1:n.*35A=
NM_000250.2:c.1486A= MANE Select NP_000241.1:p.Asn496=