Canonical Allele Identifier: CA2267631342
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273614T= , CM000679.2:g.58273614T= GRCh38
NC_000017.10:g.56350975T= , CM000679.1:g.56350975T= GRCh37
NC_000017.9:g.53705974T= NCBI36
NG_009629.1:g.12322A= , LRG_84:g.12322A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.754A=
ENST00000699291.1:c.546A= ENSP00000514272.1:p.Glu182=
ENST00000699292.1:n.461A=
ENST00000225275.4:c.1421A= MANE Select ENSP00000225275.3:p.Lys474=
ENST00000225275.3:c.1421A= ENSP00000225275.3:p.Lys474=
NM_000250.1:c.1421A= , LRG_84t1:c.1421A= NP_000241.1:p.Lys474=
XM_011524821.1:c.1607A= XP_011523123.1:p.Lys536=
XM_011524822.1:c.1136A= XP_011523124.1:p.Lys379=
XM_011524823.1:c.1446A= XP_011523125.1:p.Glu482=
NM_000250.2:c.1421A= MANE Select NP_000241.1:p.Lys474=