Canonical Allele Identifier: CA2267634603
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280396A= , CM000679.2:g.58280396A= GRCh38
NC_000017.10:g.56357757A= , CM000679.1:g.56357757A= GRCh37
NC_000017.9:g.53712756A= NCBI36
NG_009629.1:g.5540T= , LRG_84:g.5540T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.218T= MANE Select ENSP00000225275.3:p.Val73=
ENST00000225275.3:c.218T= ENSP00000225275.3:p.Val73=
ENST00000580005.1:n.147T=
NM_000250.1:c.218T= , LRG_84t1:c.218T= NP_000241.1:p.Val73=
XM_011524821.1:c.404T= XP_011523123.1:p.Val135=
XM_011524822.1:c.-38+209T= XP_011523124.1:n.-38+209T=
XM_011524823.1:c.404T= XP_011523125.1:p.Val135=
NM_000250.2:c.218T= MANE Select NP_000241.1:p.Val73=