Canonical Allele Identifier: CA2267634852
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280926T= , CM000679.2:g.58280926T= GRCh38
NC_000017.10:g.56358287T= , CM000679.1:g.56358287T= GRCh37
NC_000017.9:g.53713286T= NCBI36
NG_009629.1:g.5010A= , LRG_84:g.5010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-168A= MANE Select ENSP00000225275.3:n.-168A=
ENST00000225275.3:c.-168A= ENSP00000225275.3:n.-168A=
NM_000250.1:c.-168A= , LRG_84t1:c.-168A= NP_000241.1:n.-168A=
XM_011524821.1:c.214A= XP_011523123.1:p.Arg72=
XM_011524823.1:c.214A= XP_011523125.1:p.Arg72=
NM_000250.2:c.-168A= MANE Select NP_000241.1:n.-168A=