Canonical Allele Identifier: CA2267631345
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273621T= , CM000679.2:g.58273621T= GRCh38
NC_000017.10:g.56350982T= , CM000679.1:g.56350982T= GRCh37
NC_000017.9:g.53705981T= NCBI36
NG_009629.1:g.12315A= , LRG_84:g.12315A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.747A=
ENST00000699291.1:c.539A= ENSP00000514272.1:p.His180=
ENST00000699292.1:n.454A=
ENST00000225275.4:c.1414A= MANE Select ENSP00000225275.3:p.Met472=
ENST00000225275.3:c.1414A= ENSP00000225275.3:p.Met472=
NM_000250.1:c.1414A= , LRG_84t1:c.1414A= NP_000241.1:p.Met472=
XM_011524821.1:c.1600A= XP_011523123.1:p.Met534=
XM_011524822.1:c.1129A= XP_011523124.1:p.Met377=
XM_011524823.1:c.1439A= XP_011523125.1:p.His480=
NM_000250.2:c.1414A= MANE Select NP_000241.1:p.Met472=