Canonical Allele Identifier: CA400370177
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1475242192

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273549T>C , CM000679.2:g.58273549T>C GRCh38
NC_000017.10:g.56350910T>C , CM000679.1:g.56350910T>C GRCh37
NC_000017.9:g.53705909T>C NCBI36
NG_009629.1:g.12387A>G , LRG_84:g.12387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.819A>G
ENST00000699291.1:c.611A>G ENSP00000514272.1:n.611A>G
ENST00000699292.1:n.526A>G
ENST00000225275.4:c.1486A>G MANE Select ENSP00000225275.3:p.Asn496Asp
ENST00000225275.3:c.1486A>G ENSP00000225275.3:p.Asn496Asp
NM_000250.1:c.1486A>G , LRG_84t1:c.1486A>G NP_000241.1:p.Asn496Asp
XM_011524821.1:c.1672A>G XP_011523123.1:p.Asn558Asp
XM_011524822.1:c.1201A>G XP_011523124.1:p.Asn401Asp
XM_011524823.1:c.*35A>G XP_011523125.1:n.*35A>G
NM_000250.2:c.1486A>G MANE Select NP_000241.1:p.Asn496Asp