Canonical Allele Identifier: CA2576333034
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272673del , CM000679.2:g.58272673del GRCh38
NC_000017.10:g.56350034del , CM000679.1:g.56350034del GRCh37
NC_000017.9:g.53705033del NCBI36
NG_009629.1:g.13265del , LRG_84:g.13265del

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.1125+77del
ENST00000699291.1:c.917+77del ENSP00000514272.1:n.917+77del
ENST00000699292.1:n.1327+77del
ENST00000225275.4:c.1792+77del MANE Select ENSP00000225275.3:n.1792+77del
ENST00000225275.3:c.1792+77del ENSP00000225275.3:n.1792+77del
ENST00000577220.1:c.183+144del ENSP00000464668.1:n.183+144del
NM_000250.1:c.1792+77del , LRG_84t1:c.1792+77del NP_000241.1:n.1792+77del
XM_011524821.1:c.1978+77del XP_011523123.1:n.1978+77del
XM_011524822.1:c.1507+77del XP_011523124.1:n.1507+77del
NM_000250.2:c.1792+77del MANE Select NP_000241.1:n.1792+77del