Canonical Allele Identifier: CA2267631325
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273577C= , CM000679.2:g.58273577C= GRCh38
NC_000017.10:g.56350938C= , CM000679.1:g.56350938C= GRCh37
NC_000017.9:g.53705937C= NCBI36
NG_009629.1:g.12359G= , LRG_84:g.12359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.791G=
ENST00000699291.1:c.583G= ENSP00000514272.1:n.583G=
ENST00000699292.1:n.498G=
ENST00000225275.4:c.1458G= MANE Select ENSP00000225275.3:p.Val486=
ENST00000225275.3:c.1458G= ENSP00000225275.3:p.Val486=
NM_000250.1:c.1458G= , LRG_84t1:c.1458G= NP_000241.1:p.Val486=
XM_011524821.1:c.1644G= XP_011523123.1:p.Val548=
XM_011524822.1:c.1173G= XP_011523124.1:p.Val391=
XM_011524823.1:c.*7G= XP_011523125.1:n.*7G=
NM_000250.2:c.1458G= MANE Select NP_000241.1:p.Val486=