Canonical Allele Identifier: CA2267631259
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273463A= , CM000679.2:g.58273463A= GRCh38
NC_000017.10:g.56350824A= , CM000679.1:g.56350824A= GRCh37
NC_000017.9:g.53705823A= NCBI36
NG_009629.1:g.12473T= , LRG_84:g.12473T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.905T=
ENST00000699291.1:c.697T= ENSP00000514272.1:n.697T=
ENST00000699292.1:n.612T=
ENST00000225275.4:c.1572T= MANE Select ENSP00000225275.3:p.Arg524=
ENST00000225275.3:c.1572T= ENSP00000225275.3:p.Arg524=
ENST00000577220.1:c.30T= ENSP00000464668.1:p.Arg10=
NM_000250.1:c.1572T= , LRG_84t1:c.1572T= NP_000241.1:p.Arg524=
XM_011524821.1:c.1758T= XP_011523123.1:p.Arg586=
XM_011524822.1:c.1287T= XP_011523124.1:p.Arg429=
XM_011524823.1:c.*121T= XP_011523125.1:n.*121T=
NM_000250.2:c.1572T= MANE Select NP_000241.1:p.Arg524=