Canonical Allele Identifier: CA2638968634
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273516del , CM000679.2:g.58273516del GRCh38
NC_000017.10:g.56350877del , CM000679.1:g.56350877del GRCh37
NC_000017.9:g.53705876del NCBI36
NG_009629.1:g.12422del , LRG_84:g.12422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.854del
ENST00000699291.1:c.646del ENSP00000514272.1:n.646del
ENST00000699292.1:n.561del
ENST00000225275.4:c.1521del MANE Select ENSP00000225275.3:p.Phe508SerfsTer?
ENST00000225275.3:c.1521del ENSP00000225275.3:p.Phe508SerfsTer?
NM_000250.1:c.1521del , LRG_84t1:c.1521del NP_000241.1:p.Phe508SerfsTer?
XM_011524821.1:c.1707del XP_011523123.1:p.Phe570SerfsTer?
XM_011524822.1:c.1236del XP_011523124.1:p.Phe413SerfsTer?
XM_011524823.1:c.*70del XP_011523125.1:n.*70del
NM_000250.2:c.1521del MANE Select NP_000241.1:p.Phe508SerfsTer?