Canonical Allele Identifier: CA2267631321
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273567T= , CM000679.2:g.58273567T= GRCh38
NC_000017.10:g.56350928T= , CM000679.1:g.56350928T= GRCh37
NC_000017.9:g.53705927T= NCBI36
NG_009629.1:g.12369A= , LRG_84:g.12369A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.801A=
ENST00000699291.1:c.593A= ENSP00000514272.1:n.593A=
ENST00000699292.1:n.508A=
ENST00000225275.4:c.1468A= MANE Select ENSP00000225275.3:p.Ile490=
ENST00000225275.3:c.1468A= ENSP00000225275.3:p.Ile490=
NM_000250.1:c.1468A= , LRG_84t1:c.1468A= NP_000241.1:p.Ile490=
XM_011524821.1:c.1654A= XP_011523123.1:p.Ile552=
XM_011524822.1:c.1183A= XP_011523124.1:p.Ile395=
XM_011524823.1:c.*17A= XP_011523125.1:n.*17A=
NM_000250.2:c.1468A= MANE Select NP_000241.1:p.Ile490=