Canonical Allele Identifier: CA2267634539
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280272C= , CM000679.2:g.58280272C= GRCh38
NC_000017.10:g.56357633C= , CM000679.1:g.56357633C= GRCh37
NC_000017.9:g.53712632C= NCBI36
NG_009629.1:g.5664G= , LRG_84:g.5664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.248+94G= MANE Select ENSP00000225275.3:n.248+94G=
ENST00000225275.3:c.248+94G= ENSP00000225275.3:n.248+94G=
ENST00000580005.1:n.259+12G=
NM_000250.1:c.248+94G= , LRG_84t1:c.248+94G= NP_000241.1:n.248+94G=
XM_011524821.1:c.434+94G= XP_011523123.1:n.434+94G=
XM_011524822.1:c.-37-258G= XP_011523124.1:n.-37-258G=
XM_011524823.1:c.434+94G= XP_011523125.1:n.434+94G=
NM_000250.2:c.248+94G= MANE Select NP_000241.1:n.248+94G=
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