Canonical Allele Identifier: CA400370138
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs771572116

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273539C>A , CM000679.2:g.58273539C>A GRCh38
NC_000017.10:g.56350900C>A , CM000679.1:g.56350900C>A GRCh37
NC_000017.9:g.53705899C>A NCBI36
NG_009629.1:g.12397G>T , LRG_84:g.12397G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.829G>T
ENST00000699291.1:c.621G>T ENSP00000514272.1:n.621G>T
ENST00000699292.1:n.536G>T
ENST00000225275.4:c.1496G>T MANE Select ENSP00000225275.3:p.Arg499Leu
ENST00000225275.3:c.1496G>T ENSP00000225275.3:p.Arg499Leu
NM_000250.1:c.1496G>T , LRG_84t1:c.1496G>T NP_000241.1:p.Arg499Leu
XM_011524821.1:c.1682G>T XP_011523123.1:p.Arg561Leu
XM_011524822.1:c.1211G>T XP_011523124.1:p.Arg404Leu
XM_011524823.1:c.*45G>T XP_011523125.1:n.*45G>T
NM_000250.2:c.1496G>T MANE Select NP_000241.1:p.Arg499Leu