Canonical Allele Identifier: CA2267631297
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273532G= , CM000679.2:g.58273532G= GRCh38
NC_000017.10:g.56350893G= , CM000679.1:g.56350893G= GRCh37
NC_000017.9:g.53705892G= NCBI36
NG_009629.1:g.12404C= , LRG_84:g.12404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.836C=
ENST00000699291.1:c.628C= ENSP00000514272.1:n.628C=
ENST00000699292.1:n.543C=
ENST00000225275.4:c.1503C= MANE Select ENSP00000225275.3:p.Gly501=
ENST00000225275.3:c.1503C= ENSP00000225275.3:p.Gly501=
NM_000250.1:c.1503C= , LRG_84t1:c.1503C= NP_000241.1:p.Gly501=
XM_011524821.1:c.1689C= XP_011523123.1:p.Gly563=
XM_011524822.1:c.1218C= XP_011523124.1:p.Gly406=
XM_011524823.1:c.*52C= XP_011523125.1:n.*52C=
NM_000250.2:c.1503C= MANE Select NP_000241.1:p.Gly501=