Canonical Allele Identifier: CA2267633988
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58279455G= , CM000679.2:g.58279455G= GRCh38
NC_000017.10:g.56356816G= , CM000679.1:g.56356816G= GRCh37
NC_000017.9:g.53711815G= NCBI36
NG_009629.1:g.6481C= , LRG_84:g.6481C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.549-29C= MANE Select ENSP00000225275.3:n.549-29C=
ENST00000225275.3:c.549-29C= ENSP00000225275.3:n.549-29C=
NM_000250.1:c.549-29C= , LRG_84t1:c.549-29C= NP_000241.1:n.549-29C=
XM_011524821.1:c.735-29C= XP_011523123.1:n.735-29C=
XM_011524822.1:c.264-29C= XP_011523124.1:n.264-29C=
XM_011524823.1:c.735-29C= XP_011523125.1:n.735-29C=
NM_000250.2:c.549-29C= MANE Select NP_000241.1:n.549-29C=
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