Canonical Allele Identifier: CA2267630922
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272667G= , CM000679.2:g.58272667G= GRCh38
NC_000017.10:g.56350028G= , CM000679.1:g.56350028G= GRCh37
NC_000017.9:g.53705027G= NCBI36
NG_009629.1:g.13269C= , LRG_84:g.13269C=

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.1125+81C=
ENST00000699291.1:c.917+81C= ENSP00000514272.1:n.917+81C=
ENST00000699292.1:n.1327+81C=
ENST00000225275.4:c.1792+81C= MANE Select ENSP00000225275.3:n.1792+81C=
ENST00000225275.3:c.1792+81C= ENSP00000225275.3:n.1792+81C=
ENST00000577220.1:c.183+148C= ENSP00000464668.1:n.183+148C=
NM_000250.1:c.1792+81C= , LRG_84t1:c.1792+81C= NP_000241.1:n.1792+81C=
XM_011524821.1:c.1978+81C= XP_011523123.1:n.1978+81C=
XM_011524822.1:c.1507+81C= XP_011523124.1:n.1507+81C=
NM_000250.2:c.1792+81C= MANE Select NP_000241.1:n.1792+81C=