Canonical Allele Identifier: CA2267634649
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280495C= , CM000679.2:g.58280495C= GRCh38
NC_000017.10:g.56357856C= , CM000679.1:g.56357856C= GRCh37
NC_000017.9:g.53712855C= NCBI36
NG_009629.1:g.5441G= , LRG_84:g.5441G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.155-36G= MANE Select ENSP00000225275.3:n.155-36G=
ENST00000225275.3:c.155-36G= ENSP00000225275.3:n.155-36G=
ENST00000580005.1:n.84-36G=
NM_000250.1:c.155-36G= , LRG_84t1:c.155-36G= NP_000241.1:n.155-36G=
XM_011524821.1:c.341-36G= XP_011523123.1:n.341-36G=
XM_011524822.1:c.-38+110G= XP_011523124.1:n.-38+110G=
XM_011524823.1:c.341-36G= XP_011523125.1:n.341-36G=
NM_000250.2:c.155-36G= MANE Select NP_000241.1:n.155-36G=