Canonical Allele Identifier: CA2267631385
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273696T= , CM000679.2:g.58273696T= GRCh38
NC_000017.10:g.56351057T= , CM000679.1:g.56351057T= GRCh37
NC_000017.9:g.53706056T= NCBI36
NG_009629.1:g.12240A= , LRG_84:g.12240A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.699-27A=
ENST00000699291.1:c.491-27A= ENSP00000514272.1:n.491-27A=
ENST00000699292.1:n.379A=
ENST00000225275.4:c.1366-27A= MANE Select ENSP00000225275.3:n.1366-27A=
ENST00000225275.3:c.1366-27A= ENSP00000225275.3:n.1366-27A=
NM_000250.1:c.1366-27A= , LRG_84t1:c.1366-27A= NP_000241.1:n.1366-27A=
XM_011524821.1:c.1552-27A= XP_011523123.1:n.1552-27A=
XM_011524822.1:c.1081-27A= XP_011523124.1:n.1081-27A=
XM_011524823.1:c.1391-27A= XP_011523125.1:n.1391-27A=
NM_000250.2:c.1366-27A= MANE Select NP_000241.1:n.1366-27A=