Canonical Allele Identifier: CA400376676
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280366C>A , CM000679.2:g.58280366C>A GRCh38
NC_000017.10:g.56357727C>A , CM000679.1:g.56357727C>A GRCh37
NC_000017.9:g.53712726C>A NCBI36
NG_009629.1:g.5570G>T , LRG_84:g.5570G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.248G>T MANE Select ENSP00000225275.3:p.Ser83Ile
ENST00000225275.3:c.248G>T ENSP00000225275.3:p.Ser83Ile
ENST00000580005.1:n.177G>T
NM_000250.1:c.248G>T , LRG_84t1:c.248G>T NP_000241.1:p.Ser83Ile
XM_011524821.1:c.434G>T XP_011523123.1:p.Ser145Ile
XM_011524822.1:c.-38+239G>T XP_011523124.1:n.-38+239G>T
XM_011524823.1:c.434G>T XP_011523125.1:p.Ser145Ile
NM_000250.2:c.248G>T MANE Select NP_000241.1:p.Ser83Ile