Canonical Allele Identifier: CA2267631364
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273664G= , CM000679.2:g.58273664G= GRCh38
NC_000017.10:g.56351025G= , CM000679.1:g.56351025G= GRCh37
NC_000017.9:g.53706024G= NCBI36
NG_009629.1:g.12272C= , LRG_84:g.12272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.704C=
ENST00000699291.1:c.496C= ENSP00000514272.1:p.His166=
ENST00000699292.1:n.411C=
ENST00000225275.4:c.1371C= MANE Select ENSP00000225275.3:p.Ile457=
ENST00000225275.3:c.1371C= ENSP00000225275.3:p.Ile457=
NM_000250.1:c.1371C= , LRG_84t1:c.1371C= NP_000241.1:p.Ile457=
XM_011524821.1:c.1557C= XP_011523123.1:p.Ile519=
XM_011524822.1:c.1086C= XP_011523124.1:p.Ile362=
XM_011524823.1:c.1396C= XP_011523125.1:p.His466=
NM_000250.2:c.1371C= MANE Select NP_000241.1:p.Ile457=