Canonical Allele Identifier: CA2267631319
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273564C= , CM000679.2:g.58273564C= GRCh38
NC_000017.10:g.56350925C= , CM000679.1:g.56350925C= GRCh37
NC_000017.9:g.53705924C= NCBI36
NG_009629.1:g.12372G= , LRG_84:g.12372G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.804G=
ENST00000699291.1:c.596G= ENSP00000514272.1:n.596G=
ENST00000699292.1:n.511G=
ENST00000225275.4:c.1471G= MANE Select ENSP00000225275.3:p.Ala491=
ENST00000225275.3:c.1471G= ENSP00000225275.3:p.Ala491=
NM_000250.1:c.1471G= , LRG_84t1:c.1471G= NP_000241.1:p.Ala491=
XM_011524821.1:c.1657G= XP_011523123.1:p.Ala553=
XM_011524822.1:c.1186G= XP_011523124.1:p.Ala396=
XM_011524823.1:c.*20G= XP_011523125.1:n.*20G=
NM_000250.2:c.1471G= MANE Select NP_000241.1:p.Ala491=