Canonical Allele Identifier: CA2267634856
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280934T= , CM000679.2:g.58280934T= GRCh38
NC_000017.10:g.56358295T= , CM000679.1:g.56358295T= GRCh37
NC_000017.9:g.53713294T= NCBI36
NG_009629.1:g.5002A= , LRG_84:g.5002A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-176A= MANE Select ENSP00000225275.3:n.-176A=
ENST00000225275.3:c.-176A= ENSP00000225275.3:n.-176A=
NM_000250.1:c.-176A= , LRG_84t1:c.-176A= NP_000241.1:n.-176A=
XM_011524821.1:c.206A= XP_011523123.1:p.Asp69=
XM_011524823.1:c.206A= XP_011523125.1:p.Asp69=
NM_000250.2:c.-176A= MANE Select NP_000241.1:n.-176A=