Canonical Allele Identifier: CA2267631382
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273692G= , CM000679.2:g.58273692G= GRCh38
NC_000017.10:g.56351053G= , CM000679.1:g.56351053G= GRCh37
NC_000017.9:g.53706052G= NCBI36
NG_009629.1:g.12244C= , LRG_84:g.12244C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.699-23C=
ENST00000699291.1:c.491-23C= ENSP00000514272.1:n.491-23C=
ENST00000699292.1:n.383C=
ENST00000225275.4:c.1366-23C= MANE Select ENSP00000225275.3:n.1366-23C=
ENST00000225275.3:c.1366-23C= ENSP00000225275.3:n.1366-23C=
NM_000250.1:c.1366-23C= , LRG_84t1:c.1366-23C= NP_000241.1:n.1366-23C=
XM_011524821.1:c.1552-23C= XP_011523123.1:n.1552-23C=
XM_011524822.1:c.1081-23C= XP_011523124.1:n.1081-23C=
XM_011524823.1:c.1391-23C= XP_011523125.1:n.1391-23C=
NM_000250.2:c.1366-23C= MANE Select NP_000241.1:n.1366-23C=
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