Canonical Allele Identifier: CA2267630969
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272758G= , CM000679.2:g.58272758G= GRCh38
NC_000017.10:g.56350119G= , CM000679.1:g.56350119G= GRCh37
NC_000017.9:g.53705118G= NCBI36
NG_009629.1:g.13178C= , LRG_84:g.13178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.1115C=
ENST00000699291.1:c.907C= ENSP00000514272.1:n.907C=
ENST00000699292.1:n.1317C=
ENST00000225275.4:c.1782C= MANE Select ENSP00000225275.3:p.His594=
ENST00000225275.3:c.1782C= ENSP00000225275.3:p.His594=
ENST00000577220.1:c.183+57C= ENSP00000464668.1:n.183+57C=
NM_000250.1:c.1782C= , LRG_84t1:c.1782C= NP_000241.1:p.His594=
XM_011524821.1:c.1968C= XP_011523123.1:p.His656=
XM_011524822.1:c.1497C= XP_011523124.1:p.His499=
NM_000250.2:c.1782C= MANE Select NP_000241.1:p.His594=