Canonical Allele Identifier: CA2267631337
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273604G= , CM000679.2:g.58273604G= GRCh38
NC_000017.10:g.56350965G= , CM000679.1:g.56350965G= GRCh37
NC_000017.9:g.53705964G= NCBI36
NG_009629.1:g.12332C= , LRG_84:g.12332C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.764C=
ENST00000699291.1:c.556C= ENSP00000514272.1:p.His186=
ENST00000699292.1:n.471C=
ENST00000225275.4:c.1431C= MANE Select ENSP00000225275.3:p.Pro477=
ENST00000225275.3:c.1431C= ENSP00000225275.3:p.Pro477=
NM_000250.1:c.1431C= , LRG_84t1:c.1431C= NP_000241.1:p.Pro477=
XM_011524821.1:c.1617C= XP_011523123.1:p.Pro539=
XM_011524822.1:c.1146C= XP_011523124.1:p.Pro382=
XM_011524823.1:c.1456C= XP_011523125.1:p.His486=
NM_000250.2:c.1431C= MANE Select NP_000241.1:p.Pro477=