Canonical Allele Identifier: CA2576333172
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280275del , CM000679.2:g.58280275del GRCh38
NC_000017.10:g.56357636del , CM000679.1:g.56357636del GRCh37
NC_000017.9:g.53712635del NCBI36
NG_009629.1:g.5665del , LRG_84:g.5665del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.248+95del MANE Select ENSP00000225275.3:n.248+95del
ENST00000225275.3:c.248+95del ENSP00000225275.3:n.248+95del
ENST00000580005.1:n.259+13del
NM_000250.1:c.248+95del , LRG_84t1:c.248+95del NP_000241.1:n.248+95del
XM_011524821.1:c.434+95del XP_011523123.1:n.434+95del
XM_011524822.1:c.-37-257del XP_011523124.1:n.-37-257del
XM_011524823.1:c.434+95del XP_011523125.1:n.434+95del
NM_000250.2:c.248+95del MANE Select NP_000241.1:n.248+95del