Canonical Allele Identifier: CA2267631390
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273705A= , CM000679.2:g.58273705A= GRCh38
NC_000017.10:g.56351066A= , CM000679.1:g.56351066A= GRCh37
NC_000017.9:g.53706065A= NCBI36
NG_009629.1:g.12231T= , LRG_84:g.12231T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.699-36T=
ENST00000699291.1:c.491-36T= ENSP00000514272.1:n.491-36T=
ENST00000699292.1:n.370T=
ENST00000225275.4:c.1366-36T= MANE Select ENSP00000225275.3:n.1366-36T=
ENST00000225275.3:c.1366-36T= ENSP00000225275.3:n.1366-36T=
NM_000250.1:c.1366-36T= , LRG_84t1:c.1366-36T= NP_000241.1:n.1366-36T=
XM_011524821.1:c.1552-36T= XP_011523123.1:n.1552-36T=
XM_011524822.1:c.1081-36T= XP_011523124.1:n.1081-36T=
XM_011524823.1:c.1391-36T= XP_011523125.1:n.1391-36T=
NM_000250.2:c.1366-36T= MANE Select NP_000241.1:n.1366-36T=