Canonical Allele Identifier: CA2267634588
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280369T= , CM000679.2:g.58280369T= GRCh38
NC_000017.10:g.56357730T= , CM000679.1:g.56357730T= GRCh37
NC_000017.9:g.53712729T= NCBI36
NG_009629.1:g.5567A= , LRG_84:g.5567A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.245A= MANE Select ENSP00000225275.3:p.Glu82=
ENST00000225275.3:c.245A= ENSP00000225275.3:p.Glu82=
ENST00000580005.1:n.174A=
NM_000250.1:c.245A= , LRG_84t1:c.245A= NP_000241.1:p.Glu82=
XM_011524821.1:c.431A= XP_011523123.1:p.Glu144=
XM_011524822.1:c.-38+236A= XP_011523124.1:n.-38+236A=
XM_011524823.1:c.431A= XP_011523125.1:p.Glu144=
NM_000250.2:c.245A= MANE Select NP_000241.1:p.Glu82=