Canonical Allele Identifier: CA2267631263
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273466G= , CM000679.2:g.58273466G= GRCh38
NC_000017.10:g.56350827G= , CM000679.1:g.56350827G= GRCh37
NC_000017.9:g.53705826G= NCBI36
NG_009629.1:g.12470C= , LRG_84:g.12470C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.902C=
ENST00000699291.1:c.694C= ENSP00000514272.1:n.694C=
ENST00000699292.1:n.609C=
ENST00000225275.4:c.1569C= MANE Select ENSP00000225275.3:p.Pro523=
ENST00000225275.3:c.1569C= ENSP00000225275.3:p.Pro523=
ENST00000577220.1:c.27C= ENSP00000464668.1:p.Pro9=
NM_000250.1:c.1569C= , LRG_84t1:c.1569C= NP_000241.1:p.Pro523=
XM_011524821.1:c.1755C= XP_011523123.1:p.Pro585=
XM_011524822.1:c.1284C= XP_011523124.1:p.Pro428=
XM_011524823.1:c.*118C= XP_011523125.1:n.*118C=
NM_000250.2:c.1569C= MANE Select NP_000241.1:p.Pro523=