Canonical Allele Identifier: CA400376695
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs920327533

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280369T>G , CM000679.2:g.58280369T>G GRCh38
NC_000017.10:g.56357730T>G , CM000679.1:g.56357730T>G GRCh37
NC_000017.9:g.53712729T>G NCBI36
NG_009629.1:g.5567A>C , LRG_84:g.5567A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.245A>C MANE Select ENSP00000225275.3:p.Glu82Ala
ENST00000225275.3:c.245A>C ENSP00000225275.3:p.Glu82Ala
ENST00000580005.1:n.174A>C
NM_000250.1:c.245A>C , LRG_84t1:c.245A>C NP_000241.1:p.Glu82Ala
XM_011524821.1:c.431A>C XP_011523123.1:p.Glu144Ala
XM_011524822.1:c.-38+236A>C XP_011523124.1:n.-38+236A>C
XM_011524823.1:c.431A>C XP_011523125.1:p.Glu144Ala
NM_000250.2:c.245A>C MANE Select NP_000241.1:p.Glu82Ala