Canonical Allele Identifier: CA2267631309
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273550G= , CM000679.2:g.58273550G= GRCh38
NC_000017.10:g.56350911G= , CM000679.1:g.56350911G= GRCh37
NC_000017.9:g.53705910G= NCBI36
NG_009629.1:g.12386C= , LRG_84:g.12386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.818C=
ENST00000699291.1:c.610C= ENSP00000514272.1:n.610C=
ENST00000699292.1:n.525C=
ENST00000225275.4:c.1485C= MANE Select ENSP00000225275.3:p.Thr495=
ENST00000225275.3:c.1485C= ENSP00000225275.3:p.Thr495=
NM_000250.1:c.1485C= , LRG_84t1:c.1485C= NP_000241.1:p.Thr495=
XM_011524821.1:c.1671C= XP_011523123.1:p.Thr557=
XM_011524822.1:c.1200C= XP_011523124.1:p.Thr400=
XM_011524823.1:c.*34C= XP_011523125.1:n.*34C=
NM_000250.2:c.1485C= MANE Select NP_000241.1:p.Thr495=