Canonical Allele Identifier: CA2267630968
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272757C= , CM000679.2:g.58272757C= GRCh38
NC_000017.10:g.56350118C= , CM000679.1:g.56350118C= GRCh37
NC_000017.9:g.53705117C= NCBI36
NG_009629.1:g.13179G= , LRG_84:g.13179G=

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.1116G=
ENST00000699291.1:c.908G= ENSP00000514272.1:n.908G=
ENST00000699292.1:n.1318G=
ENST00000225275.4:c.1783G= MANE Select ENSP00000225275.3:p.Gly595=
ENST00000225275.3:c.1783G= ENSP00000225275.3:p.Gly595=
ENST00000577220.1:c.183+58G= ENSP00000464668.1:n.183+58G=
NM_000250.1:c.1783G= , LRG_84t1:c.1783G= NP_000241.1:p.Gly595=
XM_011524821.1:c.1969G= XP_011523123.1:p.Gly657=
XM_011524822.1:c.1498G= XP_011523124.1:p.Gly500=
NM_000250.2:c.1783G= MANE Select NP_000241.1:p.Gly595=