Canonical Allele Identifier: CA2267631327
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273582A= , CM000679.2:g.58273582A= GRCh38
NC_000017.10:g.56350943A= , CM000679.1:g.56350943A= GRCh37
NC_000017.9:g.53705942A= NCBI36
NG_009629.1:g.12354T= , LRG_84:g.12354T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.786T=
ENST00000699291.1:c.578T= ENSP00000514272.1:n.578T=
ENST00000699292.1:n.493T=
ENST00000225275.4:c.1453T= MANE Select ENSP00000225275.3:p.Ser485=
ENST00000225275.3:c.1453T= ENSP00000225275.3:p.Ser485=
NM_000250.1:c.1453T= , LRG_84t1:c.1453T= NP_000241.1:p.Ser485=
XM_011524821.1:c.1639T= XP_011523123.1:p.Ser547=
XM_011524822.1:c.1168T= XP_011523124.1:p.Ser390=
XM_011524823.1:c.*2T= XP_011523125.1:n.*2T=
NM_000250.2:c.1453T= MANE Select NP_000241.1:p.Ser485=