Canonical Allele Identifier: CA2267630970
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272760G= , CM000679.2:g.58272760G= GRCh38
NC_000017.10:g.56350121G= , CM000679.1:g.56350121G= GRCh37
NC_000017.9:g.53705120G= NCBI36
NG_009629.1:g.13176C= , LRG_84:g.13176C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.1113C=
ENST00000699291.1:c.905C= ENSP00000514272.1:n.905C=
ENST00000699292.1:n.1315C=
ENST00000225275.4:c.1780C= MANE Select ENSP00000225275.3:p.His594=
ENST00000225275.3:c.1780C= ENSP00000225275.3:p.His594=
ENST00000577220.1:c.183+55C= ENSP00000464668.1:n.183+55C=
NM_000250.1:c.1780C= , LRG_84t1:c.1780C= NP_000241.1:p.His594=
XM_011524821.1:c.1966C= XP_011523123.1:p.His656=
XM_011524822.1:c.1495C= XP_011523124.1:p.His499=
NM_000250.2:c.1780C= MANE Select NP_000241.1:p.His594=