Canonical Allele Identifier: CA2267631332
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273594A= , CM000679.2:g.58273594A= GRCh38
NC_000017.10:g.56350955A= , CM000679.1:g.56350955A= GRCh37
NC_000017.9:g.53705954A= NCBI36
NG_009629.1:g.12342T= , LRG_84:g.12342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.774T=
ENST00000699291.1:c.566T= ENSP00000514272.1:p.Phe189=
ENST00000699292.1:n.481T=
ENST00000225275.4:c.1441T= MANE Select ENSP00000225275.3:p.Ser481=
ENST00000225275.3:c.1441T= ENSP00000225275.3:p.Ser481=
NM_000250.1:c.1441T= , LRG_84t1:c.1441T= NP_000241.1:p.Ser481=
XM_011524821.1:c.1627T= XP_011523123.1:p.Ser543=
XM_011524822.1:c.1156T= XP_011523124.1:p.Ser386=
XM_011524823.1:c.1466T= XP_011523125.1:p.Phe489=
NM_000250.2:c.1441T= MANE Select NP_000241.1:p.Ser481=