Canonical Allele Identifier: CA2267634850
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280918A= , CM000679.2:g.58280918A= GRCh38
NC_000017.10:g.56358279A= , CM000679.1:g.56358279A= GRCh37
NC_000017.9:g.53713278A= NCBI36
NG_009629.1:g.5018T= , LRG_84:g.5018T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-160T= MANE Select ENSP00000225275.3:n.-160T=
ENST00000225275.3:c.-160T= ENSP00000225275.3:n.-160T=
NM_000250.1:c.-160T= , LRG_84t1:c.-160T= NP_000241.1:n.-160T=
XM_011524821.1:c.215+7T= XP_011523123.1:n.215+7T=
XM_011524823.1:c.215+7T= XP_011523125.1:n.215+7T=
NM_000250.2:c.-160T= MANE Select NP_000241.1:n.-160T=