Canonical Allele Identifier: CA2267631328
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273584T= , CM000679.2:g.58273584T= GRCh38
NC_000017.10:g.56350945T= , CM000679.1:g.56350945T= GRCh37
NC_000017.9:g.53705944T= NCBI36
NG_009629.1:g.12352A= , LRG_84:g.12352A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.784A=
ENST00000699291.1:c.576A= ENSP00000514272.1:p.Ter192=
ENST00000699292.1:n.491A=
ENST00000225275.4:c.1451A= MANE Select ENSP00000225275.3:p.Asp484=
ENST00000225275.3:c.1451A= ENSP00000225275.3:p.Asp484=
NM_000250.1:c.1451A= , LRG_84t1:c.1451A= NP_000241.1:p.Asp484=
XM_011524821.1:c.1637A= XP_011523123.1:p.Asp546=
XM_011524822.1:c.1166A= XP_011523124.1:p.Asp389=
XM_011524823.1:c.1476A= XP_011523125.1:p.Ter492=
NM_000250.2:c.1451A= MANE Select NP_000241.1:p.Asp484=