Canonical Allele Identifier: CA2267631339
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273610G= , CM000679.2:g.58273610G= GRCh38
NC_000017.10:g.56350971G= , CM000679.1:g.56350971G= GRCh37
NC_000017.9:g.53705970G= NCBI36
NG_009629.1:g.12326C= , LRG_84:g.12326C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.758C=
ENST00000699291.1:c.550C= ENSP00000514272.1:p.Pro184=
ENST00000699292.1:n.465C=
ENST00000225275.4:c.1425C= MANE Select ENSP00000225275.3:p.Tyr475=
ENST00000225275.3:c.1425C= ENSP00000225275.3:p.Tyr475=
NM_000250.1:c.1425C= , LRG_84t1:c.1425C= NP_000241.1:p.Tyr475=
XM_011524821.1:c.1611C= XP_011523123.1:p.Tyr537=
XM_011524822.1:c.1140C= XP_011523124.1:p.Tyr380=
XM_011524823.1:c.1450C= XP_011523125.1:p.Pro484=
NM_000250.2:c.1425C= MANE Select NP_000241.1:p.Tyr475=