Canonical Allele Identifier: CA2638975230
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280505-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280506del , CM000679.2:g.58280506del GRCh38
NC_000017.10:g.56357867del , CM000679.1:g.56357867del GRCh37
NC_000017.9:g.53712866del NCBI36
NG_009629.1:g.5430del , LRG_84:g.5430del

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.155-47del MANE Select ENSP00000225275.3:n.155-47del
ENST00000225275.3:c.155-47del ENSP00000225275.3:n.155-47del
ENST00000580005.1:n.84-47del
NM_000250.1:c.155-47del , LRG_84t1:c.155-47del NP_000241.1:n.155-47del
XM_011524821.1:c.341-47del XP_011523123.1:n.341-47del
XM_011524822.1:c.-38+99del XP_011523124.1:n.-38+99del
XM_011524823.1:c.341-47del XP_011523125.1:n.341-47del
NM_000250.2:c.155-47del MANE Select NP_000241.1:n.155-47del
Search 100 bp 5'
Search 100 bp 3'