Canonical Allele Identifier: CA400369996
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1381469903

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273510T>C , CM000679.2:g.58273510T>C GRCh38
NC_000017.10:g.56350871T>C , CM000679.1:g.56350871T>C GRCh37
NC_000017.9:g.53705870T>C NCBI36
NG_009629.1:g.12426A>G , LRG_84:g.12426A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.858A>G
ENST00000699291.1:c.650A>G ENSP00000514272.1:n.650A>G
ENST00000699292.1:n.565A>G
ENST00000225275.4:c.1525A>G MANE Select ENSP00000225275.3:p.Met509Val
ENST00000225275.3:c.1525A>G ENSP00000225275.3:p.Met509Val
NM_000250.1:c.1525A>G , LRG_84t1:c.1525A>G NP_000241.1:p.Met509Val
XM_011524821.1:c.1711A>G XP_011523123.1:p.Met571Val
XM_011524822.1:c.1240A>G XP_011523124.1:p.Met414Val
XM_011524823.1:c.*74A>G XP_011523125.1:n.*74A>G
NM_000250.2:c.1525A>G MANE Select NP_000241.1:p.Met509Val