Canonical Allele Identifier: CA2267631301
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273539C= , CM000679.2:g.58273539C= GRCh38
NC_000017.10:g.56350900C= , CM000679.1:g.56350900C= GRCh37
NC_000017.9:g.53705899C= NCBI36
NG_009629.1:g.12397G= , LRG_84:g.12397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.829G=
ENST00000699291.1:c.621G= ENSP00000514272.1:n.621G=
ENST00000699292.1:n.536G=
ENST00000225275.4:c.1496G= MANE Select ENSP00000225275.3:p.Arg499=
ENST00000225275.3:c.1496G= ENSP00000225275.3:p.Arg499=
NM_000250.1:c.1496G= , LRG_84t1:c.1496G= NP_000241.1:p.Arg499=
XM_011524821.1:c.1682G= XP_011523123.1:p.Arg561=
XM_011524822.1:c.1211G= XP_011523124.1:p.Arg404=
XM_011524823.1:c.*45G= XP_011523125.1:n.*45G=
NM_000250.2:c.1496G= MANE Select NP_000241.1:p.Arg499=