Canonical Allele Identifier: CA400376692
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.245A>T MANE Select ENSP00000225275.3:p.Glu82Val
ENST00000225275.3:c.245A>T ENSP00000225275.3:p.Glu82Val
ENST00000580005.1:n.174A>T
NM_000250.1:c.245A>T , LRG_84t1:c.245A>T NP_000241.1:p.Glu82Val
XM_011524821.1:c.431A>T XP_011523123.1:p.Glu144Val
XM_011524822.1:c.-38+236A>T XP_011523124.1:n.-38+236A>T
XM_011524823.1:c.431A>T XP_011523125.1:p.Glu144Val
NM_000250.2:c.245A>T MANE Select NP_000241.1:p.Glu82Val