Canonical Allele Identifier: CA2267634842
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280907C= , CM000679.2:g.58280907C= GRCh38
NC_000017.10:g.56358268C= , CM000679.1:g.56358268C= GRCh37
NC_000017.9:g.53713267C= NCBI36
NG_009629.1:g.5029G= , LRG_84:g.5029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-149G= MANE Select ENSP00000225275.3:n.-149G=
ENST00000225275.3:c.-149G= ENSP00000225275.3:n.-149G=
NM_000250.1:c.-149G= , LRG_84t1:c.-149G= NP_000241.1:n.-149G=
XM_011524821.1:c.215+18G= XP_011523123.1:n.215+18G=
XM_011524823.1:c.215+18G= XP_011523125.1:n.215+18G=
NM_000250.2:c.-149G= MANE Select NP_000241.1:n.-149G=