Canonical Allele Identifier: CA2267631312
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273553G= , CM000679.2:g.58273553G= GRCh38
NC_000017.10:g.56350914G= , CM000679.1:g.56350914G= GRCh37
NC_000017.9:g.53705913G= NCBI36
NG_009629.1:g.12383C= , LRG_84:g.12383C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.815C=
ENST00000699291.1:c.607C= ENSP00000514272.1:n.607C=
ENST00000699292.1:n.522C=
ENST00000225275.4:c.1482C= MANE Select ENSP00000225275.3:p.Phe494=
ENST00000225275.3:c.1482C= ENSP00000225275.3:p.Phe494=
NM_000250.1:c.1482C= , LRG_84t1:c.1482C= NP_000241.1:p.Phe494=
XM_011524821.1:c.1668C= XP_011523123.1:p.Phe556=
XM_011524822.1:c.1197C= XP_011523124.1:p.Phe399=
XM_011524823.1:c.*31C= XP_011523125.1:n.*31C=
NM_000250.2:c.1482C= MANE Select NP_000241.1:p.Phe494=