Canonical Allele Identifier: CA400373011
Community Standard Title: NM_000250.2(MPO):c.995C>G (p.Ala332Gly)
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58278036G>C , CM000679.2:g.58278036G>C GRCh38
NC_000017.10:g.56355397G>C , CM000679.1:g.56355397G>C GRCh37
NC_000017.9:g.53710396G>C NCBI36
NG_009629.1:g.7900C>G , LRG_84:g.7900C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000250.2:c.995C>G MANE Select NP_000241.1:p.Ala332Gly
ENST00000225275.4:c.995C>G MANE Select ENSP00000225275.3:p.Ala332Gly
NM_000250.1:c.995C>G , LRG_84t1:c.995C>G NP_000241.1:p.Ala332Gly
ENST00000225275.3:c.995C>G ENSP00000225275.3:p.Ala332Gly
ENST00000578493.1:n.84C>G
ENST00000578493.2:n.270C>G
ENST00000699291.1:c.281C>G ENSP00000514272.1:p.Ala94Gly
XM_011524821.1:c.1181C>G XP_011523123.1:p.Ala394Gly
XM_011524822.1:c.710C>G XP_011523124.1:p.Ala237Gly
XM_011524823.1:c.1181C>G XP_011523125.1:p.Ala394Gly