Canonical Allele Identifier: CA2638975220
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280494G>A , CM000679.2:g.58280494G>A GRCh38
NC_000017.10:g.56357855G>A , CM000679.1:g.56357855G>A GRCh37
NC_000017.9:g.53712854G>A NCBI36
NG_009629.1:g.5442C>T , LRG_84:g.5442C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.155-35C>T MANE Select ENSP00000225275.3:n.155-35C>T
ENST00000225275.3:c.155-35C>T ENSP00000225275.3:n.155-35C>T
ENST00000580005.1:n.84-35C>T
NM_000250.1:c.155-35C>T , LRG_84t1:c.155-35C>T NP_000241.1:n.155-35C>T
XM_011524821.1:c.341-35C>T XP_011523123.1:n.341-35C>T
XM_011524822.1:c.-38+111C>T XP_011523124.1:n.-38+111C>T
XM_011524823.1:c.341-35C>T XP_011523125.1:n.341-35C>T
NM_000250.2:c.155-35C>T MANE Select NP_000241.1:n.155-35C>T