Canonical Allele Identifier: CA2267634547
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280293C= , CM000679.2:g.58280293C= GRCh38
NC_000017.10:g.56357654C= , CM000679.1:g.56357654C= GRCh37
NC_000017.9:g.53712653C= NCBI36
NG_009629.1:g.5643G= , LRG_84:g.5643G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.248+73G= MANE Select ENSP00000225275.3:n.248+73G=
ENST00000225275.3:c.248+73G= ENSP00000225275.3:n.248+73G=
ENST00000580005.1:n.250G=
NM_000250.1:c.248+73G= , LRG_84t1:c.248+73G= NP_000241.1:n.248+73G=
XM_011524821.1:c.434+73G= XP_011523123.1:n.434+73G=
XM_011524822.1:c.-37-279G= XP_011523124.1:n.-37-279G=
XM_011524823.1:c.434+73G= XP_011523125.1:n.434+73G=
NM_000250.2:c.248+73G= MANE Select NP_000241.1:n.248+73G=
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