Canonical Allele Identifier: CA2267631358
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273656C= , CM000679.2:g.58273656C= GRCh38
NC_000017.10:g.56351017C= , CM000679.1:g.56351017C= GRCh37
NC_000017.9:g.53706016C= NCBI36
NG_009629.1:g.12280G= , LRG_84:g.12280G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.712G=
ENST00000699291.1:c.504G= ENSP00000514272.1:p.Pro168=
ENST00000699292.1:n.419G=
ENST00000225275.4:c.1379G= MANE Select ENSP00000225275.3:p.Arg460=
ENST00000225275.3:c.1379G= ENSP00000225275.3:p.Arg460=
NM_000250.1:c.1379G= , LRG_84t1:c.1379G= NP_000241.1:p.Arg460=
XM_011524821.1:c.1565G= XP_011523123.1:p.Arg522=
XM_011524822.1:c.1094G= XP_011523124.1:p.Arg365=
XM_011524823.1:c.1404G= XP_011523125.1:p.Pro468=
NM_000250.2:c.1379G= MANE Select NP_000241.1:p.Arg460=