Canonical Allele Identifier: CA2267631353
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273645G= , CM000679.2:g.58273645G= GRCh38
NC_000017.10:g.56351006G= , CM000679.1:g.56351006G= GRCh37
NC_000017.9:g.53706005G= NCBI36
NG_009629.1:g.12291C= , LRG_84:g.12291C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.723C=
ENST00000699291.1:c.515C= ENSP00000514272.1:p.Ala172=
ENST00000699292.1:n.430C=
ENST00000225275.4:c.1390C= MANE Select ENSP00000225275.3:p.Pro464=
ENST00000225275.3:c.1390C= ENSP00000225275.3:p.Pro464=
NM_000250.1:c.1390C= , LRG_84t1:c.1390C= NP_000241.1:p.Pro464=
XM_011524821.1:c.1576C= XP_011523123.1:p.Pro526=
XM_011524822.1:c.1105C= XP_011523124.1:p.Pro369=
XM_011524823.1:c.1415C= XP_011523125.1:p.Ala472=
NM_000250.2:c.1390C= MANE Select NP_000241.1:p.Pro464=