Canonical Allele Identifier: CA2267631304
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273542A= , CM000679.2:g.58273542A= GRCh38
NC_000017.10:g.56350903A= , CM000679.1:g.56350903A= GRCh37
NC_000017.9:g.53705902A= NCBI36
NG_009629.1:g.12394T= , LRG_84:g.12394T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.826T=
ENST00000699291.1:c.618T= ENSP00000514272.1:n.618T=
ENST00000699292.1:n.533T=
ENST00000225275.4:c.1493T= MANE Select ENSP00000225275.3:p.Phe498=
ENST00000225275.3:c.1493T= ENSP00000225275.3:p.Phe498=
NM_000250.1:c.1493T= , LRG_84t1:c.1493T= NP_000241.1:p.Phe498=
XM_011524821.1:c.1679T= XP_011523123.1:p.Phe560=
XM_011524822.1:c.1208T= XP_011523124.1:p.Phe403=
XM_011524823.1:c.*42T= XP_011523125.1:n.*42T=
NM_000250.2:c.1493T= MANE Select NP_000241.1:p.Phe498=