Canonical Allele Identifier: CA2638975845
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280891-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280893del , CM000679.2:g.58280893del GRCh38
NC_000017.10:g.56358254del , CM000679.1:g.56358254del GRCh37
NC_000017.9:g.53713253del NCBI36
NG_009629.1:g.5044del , LRG_84:g.5044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-134del MANE Select ENSP00000225275.3:n.-134del
ENST00000225275.3:c.-134del ENSP00000225275.3:n.-134del
NM_000250.1:c.-134del , LRG_84t1:c.-134del NP_000241.1:n.-134del
XM_011524821.1:c.215+33del XP_011523123.1:n.215+33del
XM_011524823.1:c.215+33del XP_011523125.1:n.215+33del
NM_000250.2:c.-134del MANE Select NP_000241.1:n.-134del
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