Canonical Allele Identifier: CA8670637
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs762653317

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273596C>T , CM000679.2:g.58273596C>T GRCh38
NC_000017.10:g.56350957C>T , CM000679.1:g.56350957C>T GRCh37
NC_000017.9:g.53705956C>T NCBI36
NG_009629.1:g.12340G>A , LRG_84:g.12340G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.772G>A
ENST00000699291.1:c.564G>A ENSP00000514272.1:p.Pro188=
ENST00000699292.1:n.479G>A
ENST00000225275.4:c.1439G>A MANE Select ENSP00000225275.3:p.Arg480His
ENST00000225275.3:c.1439G>A ENSP00000225275.3:p.Arg480His
NM_000250.1:c.1439G>A , LRG_84t1:c.1439G>A NP_000241.1:p.Arg480His
XM_011524821.1:c.1625G>A XP_011523123.1:p.Arg542His
XM_011524822.1:c.1154G>A XP_011523124.1:p.Arg385His
XM_011524823.1:c.1464G>A XP_011523125.1:p.Pro488=
NM_000250.2:c.1439G>A MANE Select NP_000241.1:p.Arg480His