Canonical Allele Identifier: CA2267631225
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273384C= , CM000679.2:g.58273384C= GRCh38
NC_000017.10:g.56350745C= , CM000679.1:g.56350745C= GRCh37
NC_000017.9:g.53705744C= NCBI36
NG_009629.1:g.12552G= , LRG_84:g.12552G=

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.954+30G=
ENST00000699291.1:c.746+30G= ENSP00000514272.1:n.746+30G=
ENST00000699292.1:n.691G=
ENST00000225275.4:c.1621+30G= MANE Select ENSP00000225275.3:n.1621+30G=
ENST00000225275.3:c.1621+30G= ENSP00000225275.3:n.1621+30G=
ENST00000577220.1:c.79+30G= ENSP00000464668.1:n.79+30G=
NM_000250.1:c.1621+30G= , LRG_84t1:c.1621+30G= NP_000241.1:n.1621+30G=
XM_011524821.1:c.1807+30G= XP_011523123.1:n.1807+30G=
XM_011524822.1:c.1336+30G= XP_011523124.1:n.1336+30G=
NM_000250.2:c.1621+30G= MANE Select NP_000241.1:n.1621+30G=