Canonical Allele Identifier: CA2267632132
Community Standard Title: NM_000250.2(MPO):c.1365+277C=
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58275265G= , CM000679.2:g.58275265G= GRCh38
NC_000017.10:g.56352626G= , CM000679.1:g.56352626G= GRCh37
NC_000017.9:g.53707625G= NCBI36
NG_009629.1:g.10671C= , LRG_84:g.10671C=

Transcript Alleles

HGVS Amino-acid Change
NM_000250.2:c.1365+277C= MANE Select NP_000241.1:n.1365+277C=
ENST00000225275.4:c.1365+277C= MANE Select ENSP00000225275.3:n.1365+277C=
NM_000250.1:c.1365+277C= , LRG_84t1:c.1365+277C= NP_000241.1:n.1365+277C=
ENST00000225275.3:c.1365+277C= ENSP00000225275.3:n.1365+277C=
ENST00000578493.2:n.698+277C=
ENST00000699291.1:c.491-1596C= ENSP00000514272.1:n.491-1596C=
XM_011524821.1:c.1551+277C= XP_011523123.1:n.1551+277C=
XM_011524822.1:c.1080+277C= XP_011523124.1:n.1080+277C=
XM_011524823.1:c.1391-1596C= XP_011523125.1:n.1391-1596C=