Canonical Allele Identifier: CA2513739294
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs2143969618

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273634del , CM000679.2:g.58273634del GRCh38
NC_000017.10:g.56350995del , CM000679.1:g.56350995del GRCh37
NC_000017.9:g.53705994del NCBI36
NG_009629.1:g.12305del , LRG_84:g.12305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.737del
ENST00000699291.1:c.529del ENSP00000514272.1:p.Ala177ProfsTer?
ENST00000699292.1:n.444del
ENST00000225275.4:c.1404del MANE Select ENSP00000225275.3:p.Pro469GlnfsTer4
ENST00000225275.3:c.1404del ENSP00000225275.3:p.Pro469GlnfsTer4
NM_000250.1:c.1404del , LRG_84t1:c.1404del NP_000241.1:p.Pro469GlnfsTer4
XM_011524821.1:c.1590del XP_011523123.1:p.Pro531GlnfsTer4
XM_011524822.1:c.1119del XP_011523124.1:p.Pro374GlnfsTer4
XM_011524823.1:c.1429del XP_011523125.1:p.Ala477ProfsTer?
NM_000250.2:c.1404del MANE Select NP_000241.1:p.Pro469GlnfsTer4