Canonical Allele Identifier: CA2267631330
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273588T= , CM000679.2:g.58273588T= GRCh38
NC_000017.10:g.56350949T= , CM000679.1:g.56350949T= GRCh37
NC_000017.9:g.53705948T= NCBI36
NG_009629.1:g.12348A= , LRG_84:g.12348A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.780A=
ENST00000699291.1:c.572A= ENSP00000514272.1:p.Gln191=
ENST00000699292.1:n.487A=
ENST00000225275.4:c.1447A= MANE Select ENSP00000225275.3:p.Asn483=
ENST00000225275.3:c.1447A= ENSP00000225275.3:p.Asn483=
NM_000250.1:c.1447A= , LRG_84t1:c.1447A= NP_000241.1:p.Asn483=
XM_011524821.1:c.1633A= XP_011523123.1:p.Asn545=
XM_011524822.1:c.1162A= XP_011523124.1:p.Asn388=
XM_011524823.1:c.1472A= XP_011523125.1:p.Gln491=
NM_000250.2:c.1447A= MANE Select NP_000241.1:p.Asn483=